Introduction

Deleterious changes in most high and moderate penetrance breast and ovarian cancer (HBOC) risk genes are causally linked with deficiencies in the DSB-response and repair by HR [1, 2]. Changes in the HBOC genes BRCA1 and BRCA2 explain a quarter of the familial risk [2]. Screening other HR genes identified additional definitive HBOC genes, including BARD1, PALB2 and BRIP1, all three encoding BRCA1-binding proteins [3]. While PALB2 serves HR by bridging the coiled-coil domain of BRCA1 with BRCA2 [4, 5], BARD1 interacts with BRCA1´s RING domain to aid BRCA1 in counteracting 53BP1 on DNA ends [6]. Through its BRCA1 C-Terminal (BRCT) domains, BRCA1 forms mutually exclusive complexes with the pSPxF-motifs containing proteins ABRAXAS1 (alias ABRA1, CCDC98, FAM175A) [7,8,9], BRIP1 (BRCA1 interacting protein C-terminal helicase 1, alias BACH1, FANCJ) [10, 11] and CTIP (C-terminal binding protein-interacting protein, alias RBBP8) [12, 13]. These three CDK-mediated, phosphorylation-dependent interactions result in formation of BRCA1-A to -C complexes in S- and G2-phase of the cell cycle [14].

Of particular interest for this work, ABRAXAS1 serves as adapter of BRCA1-A complex components BRCA1, RAP80, MERIT40, BRCC45 and BRCC36 [9, 15,16,17]. In this way, BRCA1-A (i) accumulates BRCA1 at DSBs via RAP80-mediated recognition of Lys63-linked ubiquitin (K63Ub) adducts in the damaged chromatin [9, 15, 18], (ii) terminates the DDR via BRCC36-mediated K63Ub deubiquitinase (DUB)-activity [19] and (iii) prevents over-resection through sequestration of BRCA1 to the flanks of the DSBs, thereby depleting the local pool of BRCA1 available to enhance DNA end-resection by BRCA1-C [20]. In BRCA1-C, CTIP and MRE11–RAD50–NBS1 (MRN) initiate end-resection at DSBs and therefore HR [21, 22]. There has been a debate on whether BRCA1-A is necessary to ensure proper execution of HR [7, 9, 15, 18, 23] or to prevent excessive HR through antagonizing DSB end-resection [24, 25]. Nevertheless, there is a general consensus on that the localization of the BRCA1-A complex at DNA damage sites is crucial for repair, DDR and genome stability.

ABRAXAS1 germline variants have been described in Northern Finnish high-risk breast cancer families [23] and in the germline of Non-Finnish cancer patients [1, 26,27,28,29]. Yet, a case-control screening study of ABRAXAS1 missense and non-coding mutations in non-isolated populations of the Breast Cancer Family Registry did not reveal significant association with breast cancer risk [30]. Here, we identified and functionally characterized two ABRAXAS1 germline mutations in early-onset breast cancer patients from Germany: ABRAXAS1 c.1106dup, previously identified in the germline of two ovarian cancer patients of a US-Swedish cohort with family history of the disease [1], a US triple-negative breast cancer patient [27] and three further cancer patients [26, 28, 29] but not in the Flossies project of ~10000 cancer-free women >70 (https://whi.color.com/). ABRAXAS1 c.577C>T was newly identified in patients and recorded once in the Flossies project. Our analysis of functions associated with these ABRAXAS1 variants revealed a dominant effect of the two truncated ABRAXAS1 proteins on de-repression of the mutagenic DSBR-pathway SSA, yet in different ways, namely by a shift of BRCA1 from BRCA1-A into -C complexes in case of c.1106dup and enhanced formation of the total number of MRE11 complexes as part of excessive stress signaling in case of c.577C>T.

Results

Comparative analysis of BRCA1-A complex formation in cells from early-onset breast cancer patients with truncating ABRAXAS1-mutations

We studied DDRs in cells from heterozygous ABRAXAS1-mutation carriers to understand whether breast cancer-associated mutations in the gene encoding the BRCA1 complex partner ABRAXAS1 entail similar phenotypic changes as described for BRCA1-mutations. To this end we engaged LCLs ABR-1106, ABR-577 and ABR-wt from two German mutation carriers (c.1106dup, c.577C>T) and one healthy family member with wild-type ABRAXAS1, respectively (Supplementary Table S1). In parallel, we analyzed LCL BR-0968 as representative external healthy wild-type control from a previous study [31]. Strikingly, in both ABRAXAS1-mutation carriers breast cancer was diagnosed at early age (25 years). Both mutations caused truncations, thereby deleting the C-terminal BRCA1-binding region in case of ABRAXAS1 c.1106dup, p.(Ser370Ilefs*2) and the BRCA1- plus BRCC36-interaction sites in case of ABRAXAS1 c.577C>T, p.(Arg193*) (Fig. 1a). Western blotting engaging mAbs recognizing the C-terminal amino acids 394–408 demonstrated reduction of full-length ABRAXAS1 protein down to on average 60% in cells from heterozygous mutation carriers when compared to the controls (Supplementary Fig. S1a). Concomitantly, BRCA1 levels showed a trend of downregulation to ~70% in ABRAXAS1-mutated LCLs (Supplementary Fig. S1b).

Fig. 1: Analysis of ABRAXAS1- and BRCA1-foci accumulation in response to IR.
figure 1

Wild-type ABRAXAS1 (ABR-wt: white), ABRAXAS1 c.1106dup-mutated (ABR-1106: light grey) and ABRAXAS1 c.577C>T-mutated (ABR-577: dark grey) LCLs were either exposed to γ-irradiation with a dose of 2 Gy (IR) followed by cultivation for 4 h or left untreated. Foci per nucleus were scored by automated quantification of 50 nuclei from three independent experiments each and normalized to the mean foci numbers per nucleus calculated from irradiated wild-type LCLs (ABR-wt and external control BR-0968) measured on the same day, which were defined as 100%. GraphPad Prism software was used for graphic presentation and calculation of statistically significant differences via Kruskal–Wallis test followed by two-tailed Mann–Whitney U test comparing mean values in ABR-wt, ABR-1106 and ABR-577 under untreated or IR-treated conditions. Columns show mean values; n = 150; bars, SEM; **P < 0.01, ***P < 0.001, ****P < 0.0001. a Schematic drawings visualizing the truncated mutant proteins ABRAXAS1 p.(Ser370Ilefs*2) encoded by ABRAXAS1 c.1106dup with deletion of the C-terminal BRCA1-interaction site (comprising a SPTF motif, amino acids 406–409, [23]) and of ABRAXAS1 p.(Arg193*) encoded by ABRAXAS1 c.577C>T additionally devoid of the BRCC36-interaction site (amino acids 200–270, [65]). Both proteins retain most of the ABR domain mediating interactions with BRCC45, MERIT40 and RAP80. Green, truncated proteins; NLS nuclear localization signal, pSPTF phosphoserine motif that binds to the BRCT domains of BRCA1 [23]. b Graphic presentation of ABRAXAS1-foci per nucleus (absolute values corresponding to 100%: 4.2). c Graphic presentation of BRCA1-foci per nucleus (absolute values corresponding to 100%: 5.6). d Graphic presentation of ABRAXAS1/BRCA1 co-localizing foci (absolute values corresponding to 100%: 4.8). e Representative images of ABRAXAS1 (red) and BRCA1 (green) in DAPI-stained nuclei (blue). The scale bars here and further on represent 10 μm.

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To understand whether these changes in protein levels also impact on formation of DNA damage-associated protein complexes, we performed quantitative immunofluorescence microscopy of nuclear proteins in cells 4 h after treatment with 2 Gy ionizing radiation (IR), when ABRAXAS1 signals peaked (data not shown). ABRAXAS1 showed tenfold reduced foci numbers in ABR-1106 compared with ABR-wt independently of IR (Fig. 1b). ABR-577 displayed normal ABRAXAS1-foci numbers pre-IR and 21% reduction post-IR. IR-induced foci increases seen for ABR-wt were neither detectable for ABR-1106 nor ABR-577. Surprisingly, BRCA1-foci were two- and threefold elevated in ABR-577 compared with ABR-wt before and after IR (Fig. 1c). Differently, ABR-1106 formed BRCA1-foci twofold less efficiently post-IR. Yet, IR-induced formation was observed in all three cell types. Thus, despite decreases in overall protein levels, ABRAXAS1-foci numbers were constitutively high in ABR-577 and BRCA1-foci numbers also elevated. In ABR-1106 ABRAXAS1 and to a lesser extent also BRCA1-foci formation were compromised.

When inspecting foci overlays, co-localization of ABRAXAS1- with BRCA1-foci was readily noticeable in ABR-wt, and showed a fivefold increase post-IR (Fig. 1d, e). In both ABRAXAS1-mutated LCLs we observed a fraction of BRCA1-foci without ABRAXAS1 co-localization, and colocalizing foci post-IR amounted to only ~40% of the ones in ABR-wt. To directly count multi-protein complexes containing both BRCA1 and ABRAXAS1, named BRCA1-A [32], we engaged PLA. As depicted in Fig. 2, PLA-foci marking association of ABRAXAS1 and BRCA1 were reduced down to half in ABR-1106 and ABR-577 compared to untreated wild-type cells. In IR-treated cells PLA-foci were reduced by 23% in ABR-1106 but not ABR-577. Differences between PLA and co-localization data have been observed before and may be due to the higher sensitivity and spatial resolution of PLA [33]. Altogether, our data suggest compromised BRCA1-A complex formation at DSBs in ABRAXAS1 c.1106dup-mutated cells, and to some extent also in ABRAXAS1 c.577C>T-mutated cells despite excessive BRCA1-foci numbers.

Fig. 2: Analysis of BRCA1 and ABRAXAS1 associations.
figure 2

Association between BRCA1 and ABRAXAS1 was examined in LCLs ABR-wt, ABR-1106 and ABR-577 with wild-type ABRAXAS1 (white columns), with ABRAXAS1 c.1106dup (light grey column) and ABRAXAS1 c.577C>T (dark grey column), respectively, via PLA. LCLs were either exposed to IR and re-cultivated for 4 h or left untreated. PLA-foci were scored by automated quantification of 100 nuclei for each time-point in three independent experiments each and normalized to the mean PLA-foci values of the wild-type control ABR-wt 4 h post IR (absolute values corresponding to 100%: PLA, 7.3). Columns show mean values; n = 300; bars, SEM; **P < 0.01, ***P < 0.001; ****P < 0.0001. Statistically significant differences were calculated via Kruskal–Wallis test followed by two-tailed Mann–Whitney U test comparing mean values for different LCLs. a Graphic presentation of ABRAXAS1/BRCA1 PLA-foci per nucleus (%). b Representative images of PLA-foci (red) using primary antibodies anti-BRCA1 (mouse) and anti-ABRAXAS1 (rabbit) in DAPI-stained nuclei (blue). Negative controls without the primary (1st) and secondary (2nd) antibody (Ab), respectively, were performed to validate the specificity of the stainings.

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Aberrant DSBR-pathway usage in cells with truncating ABRAXAS1-mutations

Next, we investigated whether imbalanced BRCA1-A complex formation in ABRAXAS1-mutated cells impacted on DSBR-pathway usage as previously described for cells from predisposed individuals with heterozygous BRCA1- or BRCA2-mutations [34,35,36]. Therefore, we employed EGFP-based reporter substrates enabling specific analyses of DSBR by HR, NHEJ, MMEJ and SSA (Fig. 3a). BRCA1-A complex is known to regulate HR [24]. ABR-577 displayed threefold increased frequencies of HR, however, also of the competing NHEJ-pathway, when compared with the wild-type control. In contrast, HR as well as NHEJ were unaltered in ABR-1106. MMEJ measurements did not reveal a significant change in the ABRAXAS1-mutated cells. Intriguingly however, SSA-frequencies were twofold enhanced in both ABRAXAS1 c.1106dup- and c.577C>T-mutated cells.

Fig. 3: DSBR pathway usage in cells expressing mutated versus wild-type ABRAXAS1.
figure 3

Repair events were analyzed by flow cytometry 48 h after transfection of LCLs with EGFP-based and pathway-specific DSBR reporter plasmids plus I-SceI meganuclease expression plasmid. Percentages of EGFP-positive cells in the live cell population were individually corrected for transfection efficiencies obtained in split culture samples transfected with the same plasmid mixture but replacing a filler plasmid by wild-type EGFP expression plasmid (triplicates for repair events and triplicates for transfection efficiencies each). Resulting DSBR frequencies were normalized to the mean frequencies for controls measured on the same day, namely for both wild-type ABRAXAS1 cell lines in (a) and for wild-type ABRAXAS1 cells transfected with empty vector in (b). These reference values were defined as 100% (corresponding to 3.7 × 10−4 for HR, 3.9 × 10−3 for NHEJ, 5.3 × 10−4 for MMEJ, 2.5 × 10−3 for SSA). Columns show DSBR frequencies; bars, SEM; GraphPad Prism software was used for graphic presentation and calculation of statistically significant differences via Kruskal–Wallis-test followed by two-tailed Mann–Whitney U test. *P < 0.05, **P < 0.01, **** P < 0.0001; a DSBR in heterozygously ABRAXAS1-mutated and wild-type individuals. LCLs from two wild-type ABRAXAS1 individuals (ABR-wt: white columns and external control BR-0968: hatched), one ABRAXAS1 c.1106dup (ABR-1106: light grey) and one ABRAXAS1 c.577C>T (ABR-577: dark grey) mutation carrier were transfected with a DNA mixture containing reporter constructs for analysis of HR, NHEJ, MMEJ or SSA (schematically drawn on the left side of each panel [80, 79]). Statistically significant differences were calculated between the mean values in ABR-wt, ABR-1106 and ABR-577. n = 15 from five independent experiments; b DSBR after ectopic expression of ABRAXAS1 variants. LCL ABR-wt cells were co-transfected with plasmid mixtures for HR, NHEJ or SSA measurements including I-SceI meganuclease expression plasmid (see a) plus expression plasmids for wild-type ABRAXAS1 (wt: white), the mutated variants (dup, ABRAXAS1 c.1106dup: light grey; c.577, ABRAXAS1 c.577C>T: dark grey) or empty vector (ctrl: hatched). Statistically significant differences were calculated between the mean values in cells expressing exogenous wild-type versus mutated ABRAXAS1. n = 6–9 from two to three independent experiments.

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To test whether the changes in DSBR-pathway usage can indeed be explained by the truncated ABRAXAS1 proteins, we ectopically expressed them in comparison with wild-type protein in control cells (ABR-wt) (Supplementary Fig. S2a). Expression of both mutant proteins, encoded by ABRAXAS1 c.1106dup and c.577C>T, stimulated SSA twofold compared with wild-type (Fig. 3b). We also observed a twofold increase in HR- and NHEJ-frequencies when ectopically expressing c.577C>T-encoded ABRAXAS1, altogether, mimicking the differences seen with mutation carrier versus control cells. Moreover, we performed DSBR measurements in the chromatin context after ectopic expression of ABRAXAS1 variants together with meganuclease I-SceI cleaving a chromosomally integrated reporter. The results show that homologous repair, RAD52-dependent SSA, in particular [37], rose 1.4- to 1.5-fold in cells expressing mutated ABRAXAS1 (Supplementary Fig. S2b, c). These data excluded the possibility that the differences observed with LCLs were due to clonal particularities demonstrating true effects of the truncated ABRAXAS1 proteins.

To interrogate a key step during HR [38], we scored formation of RAD51 nucleoprotein filaments by immunofluorescence microscopy. While we observed that RAD51-foci numbers rose in all IR-treated cells, we did not observe a statistically significant difference in ABRAXAS1-mutated versus wild-type cells (Supplementary Fig. S3a, left panel, and b). However, basal RAD51-foci numbers were reduced in ABR-577 down to 26% compared with ABR-wt. Loss of HR function has been connected with hypersensitivity to poly(ADP-ribose)polymerase (PARP) inhibition [39, 40]. Measurements of the concentration-dependent cell viabilities of LCLs following PARP-inhibitor treatment (1,5-isoquinolinediol, IQD) did not reveal a statistically significant change of IC50-values in ABRAXAS1-mutated cells compared with the wild-type (Supplementary Fig. S4a). For comparison, when analyzing BRCA2-mutated cells, we observed increased sensitivity in carriers of bi-allelic but again not mono-allelic mutation carriers (Supplementary Fig. S4b). Altogether and as similarly noticed in previous studies with LCLs from heterozygous BRCA1-, BRCA2- and PALB2-mutation carriers [31, 34, 36], mono-allelic mutation of ABRAXAS1 did not cause a defect in HR but de-repression of SSA.

Aberrant DDRs in cells with ABRAXAS1 c.577C>T

To provide insight into the mechanism underlying aberrant DSBR-activities in ABRAXAS1-mutated cells, we investigated the hallmarks of DDRs by immunofluorescence microscopy [41, 42]. To investigate recruitment of 53BP1 to DSBs and subsequent clearance we performed time course experiments post-IR (Supplementary Fig. S5a, b). Strikingly, focal nuclear signals were consistently elevated in ABR-577 before and after IR-treatment when compared with ABR-1106 (up to 12-fold) as well as with ABR-wt (up to fivefold). Conversely, ABR-1106 formed 53BP1-foci less efficiently than ABR-wt (down to 28%). When focusing on the small number of gigantic 53BP1 bodies, known to shield under-replicated DNA outside of S-phase [43], we obtained a similar pattern (Supplementary Fig. S5c). Next, we scored the DNA damage marker γH2AX, i.e. focal phosphorylation of Ser139 in H2AX. γH2AX-foci were at least sixfold higher in untreated and at least twofold higher in irradiated ABR-577 compared with ABR-wt and ABR-1106 (Fig. 4a, d).

Fig. 4: Monitoring replication stress and DSB responses.
figure 4

Wild-type ABRAXAS1 (ABR-wt: white and external control BR-0968: hatched), ABRAXAS1 c.1106dup (ABR-1106: light grey) and ABRAXAS1 c.577C>T (ABR-577: dark grey) LCLs were IR-treated and re-cultivated for 4 h (a–d). Foci per nucleus were scored by automated quantification and normalized to the mean foci numbers per nucleus calculated from irradiated wild-type LCLs (ABR-wt and external control BR-0968) measured on the same day (100%). Calculation of statistically significant differences between mean values in the LCLs ABR-wt, ABR-1106 and ABR-577 via Kruskal–Wallis test followed by two-tailed Mann–Whitney U test. Columns show mean values; bars, SEM; *P < 0.05, ***P < 0.001, ****P < 0.0001. a γH2AX-foci per nucleus (n = 150–200 from three independent experiments; absolute values corresponding to 100%: 7.2). (b) MRE11-foci per nucleus (n = 100 from two independent experiments; absolute values corresponding to 100%: 1.9). c RPA-foci per nucleus (n = 100 from two independent experiments; absolute values corresponding to 100%: 10.3). d Representative images of foci (γH2AX: green, MRE11: red, RPA: green) in DAPI-stained nuclei (blue). e Analysis of RPA32 and KAP1 phosphorylation. Representative western blot (n = 2) showing immunodetection of KAP1 phosphorylated on Ser824, RPA32 on Ser33 and total KAP1 as well as RPA32 in control LCL transfected with expression plasmids for wild-type (wt) or mutant ABRAXAS1 variants (dup, ABRAXAS1 c.1106dup; C>T, ABRAXAS1 c.577C>T) followed by 48 h of unperturbed growth (untreated) or 24 h of growth, IR and recultivation for 4 h (4 h post IR). Detection of Tubulin served as loading control. Uncropped western blots are shown in Extended Figure E2.

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When DNA ends are resected for HR or SSA, the endo-/exonuclease MRE11 is critically involved in initial processing. The resulting single-stranded DNA (ssDNA) is immediately coated by RPA to protect it from degradation [44]. Microscopic analysis indicated threefold elevated MRE11- and ≥twofold elevated RPA-foci levels in ABR-577 post-IR as compared with the other cell types (Fig. 4b–d). Basal MRE11-foci were twofold higher in ABR-577 compared with ABR-wt, RPA-foci ≥fivefold compared with the other cell types. In ABR-1106 MRE11-foci remained at wild-type level regardless of treatment. RPA-foci rose ≥2.5-fold versus wild-type controls post-IR, reaching statistical significance when compared with BR-0968 (****P < 0.0001).

During replication stress the checkpoint kinase ATR phosphorylates Ser33 in RPA while bound to ssDNA [45]. When we monitored phosphorylation of RPA32 at Ser33 by western blotting, we noticed a rise of pRPA32/RPA normalized band intensities in control LCL cells ectopically expressing ABRAXAS1 c.1106dup or c.577C>T compared to wild-type by on average twofold (Fig. 4e). For comparison, we also analyzed phosphorylation of the ATM substrate KAP1 on Ser824 in these samples [46], showing comparable IR-induced KAP1 phosphorylation upon expression of all three ABRAXAS1 variants (<10% differences of pKAP1/KAP1). We conclude that ATR rather than ATM signaling was active in cells expressing mutated ABRAXAS1 variants due to endogenous stress.

HR factors can protect replication forks from MRE11-dependent degradation independently of their recombination-activities [6, 47]. Therefore, we analyzed DNA replication stress as a mechanism potentially underlying constitutively enhanced MRE11-activities in ABR-577. To this end we performed DNA fiber spreading assays with sequential incorporation of CldU and IdU interrupted by hydroxyurea (HU) treatment provoking MRE11-dependent attack of nascent DNA (Supplementary Fig. S6a). Measurement of CldU-positive replication track lengths did reveal the expected track shortening upon HU- versus mock-treatment (Supplementary Fig. S6b). Yet, despite elevated MRE11- and RPA-foci in ABR-577, DNA replication tracks were not shortened but elongated (1.3-fold) in cells ectopically expressing ABRAXAS1 c.577C>T compared to wild-type. Analysis of the percentage of aberrant CldU/IdU replication track ratios did not carve out any differences (Supplementary Fig. S6c). Altogether, these data sets argue against major differences in replication fork stalling or fork degradation.

Given that ABR-577 showed dramatic DDRs already in the untreated state, we tested whether the mutations also affect the genomic stability by quantification of micronuclei post-IR. Strikingly, we noticed up to fivefold higher micronucleus numbers in ABR-1106 with compromised 53BP1-foci formation (Fig. 5a). Next, we analyzed the activation of cell cycle checkpoints [32]. Flow cytometric analysis revealed a similar distribution of ABR-wt and ABR-1106 in the cell cycle phases G1, S and G2/M (Fig. 5b, c). However, ABR-577 showed a three times higher percentage of G2/M-phase cells (Fig. 5c, d). Concomitantly, cell death was reduced in these cells compared to ABR-wt and ABR-1106. However, when we transiently expressed ABRAXAS1 variants in control LCLs, we observed 1.2- to 1.3-fold G2/M-accumulation in cells expressing c.1106dup versus wild-type for 24 h and 48 h (Supplementary Fig. S7a, b). IR-treatment 24 h post transfection elevated G2/M-DNA contents 1.4-fold in cells expressing both c.1106dup and c.577C>T but not wild-type. Forty-eight hours and 72 h post transfection all cell types showed a similar IR-induced G2/M-accumulation. No significant changes were seen in the percentages of cells with subG1-DNA content (Supplementary Fig. S7c). To specifically detect cell death by apoptosis, we monitored accumulation of the cleaved form of PARP1 by western blotting. We observed appearance in irradiated cells, whereby cleaved PARP signals rose in cells ectopically expressing mutated versus wild-type ABRAXAS1, particularly c.577C>T (Supplementary Fig. S7d). Altogether, in LCLs constitutively expressing mutated ABRAXAS1 we observed pronounced G2/M-accumulation for c.577C>T, in transiently expressing cells minor accumulation for mutated variants, but particularly pronounced IR-induced apoptosis for c.577C>T. In conclusion, ABR-1106 cells showed reduced 53BP1-foci numbers accompanied by micronucleus formation indicating genomic instability, while ABR-577 cells were particular in that they displayed exacerbated DDRs.

Fig. 5: Micronuclei and cell cycle distribution.
figure 5

a Quantification of micronucleus formation. LCLs derived from wild-type ABRAXAS1 individual (ABR-wt) and from the ABRAXAS1 c.1106dup (ABR-1106) and the ABRAXAS1 c.577C>T (ABR-577) mutation carriers were exposed to IR and re-cultivated before cells were fixed at the indicated time points. Micronuclei per nucleus were scored and normalized to the mean value of ABR-wt 1 h post IR measured on the same day each. This reference value (100%) represents four micronuclei/100 nuclei. Statistically significant differences between values for LCLs ABR-wt, ABR-1106 and ABR-577 for each treatment condition and pairwise for untreated cells and 1 h post IR were calculated via Kruskal–Wallis test followed by two-tailed Mann–Whitney U test. Data points indicate mean values and SEM of 150 nuclei obtained from three experiments. *P < 0.05, **P < 0.01, ***P < 0.001. The image on the right shows a representative microscopic image of a DAPI-stained nucleus with micronucleus at the tip of the white arrow. b DNA content was determined flow cytometrically after propidium iodide staining of LCLs from external wild-type control BR-0968, ABR-wt, ABR-1106 and ABR-577. Cell cycle distribution of G1-, S- and G2/M-phases in living cells is graphically presented. c Representative histograms of propidium iodide stained LCLs. d Statistically significant differences between the mean percentages of cells with G2/M-phase and subG1-DNA content were calculated for ABR-wt, ABR-1106 and ABR-577 via Kruskal–Wallis-test followed by two-tailed Mann–Whitney U test (n = 4 from two independent experiments); bars, SEM; *P < 0.05.

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Given that RAD51 expression is cell cycle-dependent [48], we scored RAD51-foci in LCL cells ectopically expressing the different ABRAXAS1 proteins for 24 h, i.e. causing minor cell cycle changes. Under these conditions the pattern of RAD51-foci accumulation was similar as seen in patient-derived cells except for threefold lower foci numbers 4 h post IR in cells expressing c.577C>T versus wild-type ABRAXAS1 (Supplementary Fig. S3a, right panel). These data suggest that RAD51 filament formation at DSBs is compromised in LCLs transiently expressing ABRAXAS1 c.577C>T, which is rescued in constitutively expressing patient-derived LCLs due to an exacerbated DDR.

ABRAXAS1 c.1106dup shifts BRCA1 into the BRCA1-C complex

To analyze patient-derived ABRAXAS1-mutations in breast epithelial cells, we performed CRISPR/Cas9-based knockout (KO) in immortalized, non-cancer MCF10A cells. ABRAXAS1-KO resulted in bi-allelic deletion of 47 bp encompassing the ABRAXAS1 start codon in clone D1; in clone E7, 11 bp were deleted around the start codon on one allele and 16 bp in combination with a 1410 bp insertion on the second allele (Supplementary Fig. S8a, b). Expression analysis verified complete loss of ABRAXAS1 mRNA in clone D1; in E7 residual levels were detectable (Supplementary Fig. S8c). When examining ABRAXAS1-foci, we noticed 5- to 11-fold induction post-IR in parental MCF10A and the A9 control clone (Fig. 6a). Consistent with mRNA expression, nuclear ABRAXAS1 signals were at the detection limit in KO clone D1 regardless of IR-treatment, whereas residual ABRAXAS1-foci were detectable in E7 post-IR. Consequently, we chose D1 for analysis of exogenous ABRAXAS1 proteins in the following experiments.

Fig. 6: DDR in mammary epithelial cells as a function of ABRAXAS1.
figure 6

Mammary epithelial control MCF10A cells (parental and clone A9) and ABRAXAS1 KO cells (clones D1 and E7) were nucleofected with expression plasmids for wild-type ABRAXAS1 (wt), the mutated variants (dup, ABRAXAS1 c.1106dup; C>T, ABRAXAS1 c.577C>T) or empty vector (ctrl), irradiated 24 h later with a dose of 2 Gy and re-cultivated for another 2 h. Nuclear foci were scored and normalized to mean foci numbers of controls on the same experimental day (100%). Columns show mean values (n = 100–400 from two to four independent experiments); bars, SEM; Kruskal–Wallis test followed by two-tailed Mann–Whitney U test; *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001. a ABRAXAS1-foci per nucleus in the different cell types with and without IR (absolute values corresponding to 100%: 8.9 in irradiated parental MCF10A cells). b–d Foci per nucleus in control (A9) and ABRAXAS1 KO cells (D1) after expression of different ABRAXAS1 proteins and IR-treatment for 2 h. b ABRAXAS1-foci per nucleus (A9 10.3, D1: 3.1 corresponding to 100% in cells expressing wt). c BRCA1-foci per nucleus (A9: 1.2, D1: 0.9 corresponding to 100% in cells expressing wt). d MRE11-foci per nucleus (A9: 1.9, D1: 2.1 corresponding to 100% in cells expressing wt).

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To compare ABRAXAS1 c.1106dup, c.577C>T and wild-type expression in ABRAXAS1-negative and -positive backgrounds, we ectopically expressed these variants in ABRAXAS1-KO- and control MCF10A cells (Supplementary Fig. S8d). Re-expression of wild-type but not mutant ABRAXAS1 reconstituted IR-induced ABRAXAS1-foci formation in KO cells (Fig. 6b, Supplementary Fig. S8e). In ABRAXAS1-positive control cells, we counted fewer ABRAXAS1-foci after expression of the c.1106dup variant versus wild-type or c.577C>T, compatible with an inhibitory effect on foci formation by endogenous ABRAXAS1, already seen in heterozygously mutated LCLs (Fig. 1b). BRCA1-foci numbers post-IR were lower in KO cells ectopically expressing c.1106dup versus wild-type, whereby generally low BRCA1-foci numbers in MCF10A cells did not permit to carve out further statistically significant differences (Fig. 6c). Analysis of MRE11-foci in KO cells post-IR showed that ABRAXAS1 c.1106dup expression increased foci counts compared with all other samples (Fig. 6d). In ABRAXAS1-positive control cells, maximum MRE11 signals were observed after c.577C>T expression, similar to LCL ABR-577 where this variant stimulated DDRs. In MCF10A cells checkpoint activation after mutant ABRAXAS1 expression was exerted in G1, which reached statistical significance when comparing fold changes between the group of KO cells expressing mutated ABRAXAS1 (c.1106dup or c.577C>T) with the other KO cells (expressing wild-type or no ABRAXAS1, Supplementary Fig. S9a–c).

Inspired by the fact that MRE11-foci formation was enhanced in IR-treated cells expressing endogenous wild-type ABRAXAS1 plus c.577C>T in different cell types (Figs. 4b and 6d), we asked whether unleashed MRE11-dependent end-processing (Fig. 4c) and SSA (Fig. 3) were accompanied by BRCA1-association with MRE11 within BRCA1-C [32]. Surprisingly, ectopic expression of ABRAXAS1 c.577C>T in ABR-wt did not alter the association of MRE11 and BRCA1 versus wild-type. However, expression of c.1106dup doubled MRE11/BRCA1 PLA-foci post-IR (Fig. 7a). Together with our finding that BRCA1-A complex formation was compromised in ABR-1106 (Figs. 1d and 2a), these data suggest a shift of BRCA1 from BRCA1-A to –C in cells expressing ABRAXAS1 devoid of the extreme C-terminus.

Fig. 7: Analysis of BRCA1-C complex formation and model for functional defects of ABRAXAS1 mutant proteins.
figure 7

a Analysis of MRE11 and BRCA1 associations. LCL ABR-wt was transfected 24 h before IR with expression plasmids for wild-type (wt) or mutant ABRAXAS1 variants (dup, ABRAXAS1 c.1106dup; C>T, ABRAXAS1 c.577C>T). PLA was performed 4 h post IR. MRE11/BRCA1 PLA-foci were scored by automated quantification of 150 nuclei from three independent experiments and normalized to the mean for the external control transfected with empty vector, which was defined as 100% (0.2). Columns show mean values; n = 450; bars, SEM; Kruskal–Wallis test followed by two-tailed Mann–Whitney U test; **P < 0.01, ***P < 0.001, ****P < 0.0001. The right panel shows representative images of PLA-foci (red) 4 h post IR using primary antibodies anti-MRE11 (rabbit) and anti-BRCA1 (mouse) in DAPI-stained nuclei (blue). b Model for the findings revealing how the truncated ABRAXAS1 mutant proteins differentially deregulate DSBR. See main text for details. In brevity, ABRAXAS1 p.(Ser370Ilefs*2), encoded by ABRAXAS1 c.1106dup, cannot bind the C-terminal BRCT domains of BRCA1, therefore giving access to CTIP and MRE11-RAD50-NBS1. This causes a shift of BRCA1-A to BRCA1-C complex formation, which spurs end-processing and SSA at DSBs. ABRAXAS1 p.(Arg193*), encoded by ABRAXAS1 c.577C>T, additionally cannot bind BRCC36, which therefore cannot limit the DSB-induced ubiquitination cascade, entailing excess DNA damage signaling and unspecific DSBR-activities. Red color marks the impact of ABRAXAS1 mutant proteins on biochemical processes underlying the observed changes in DSBR.

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Discussion

In this work, we investigated functional consequences of the ABRAXAS1-variants c.1106dup and c.577C>T identified in two German patients with early-onset breast cancer. ABRAXAS1 physically links BRCA1 to the other BRCA1-A complex components, i.e. to BRCC45, MERIT40, BRCC36 and RAP80, thereby accumulating BRCA1 adjacent to DSBs [49]. While BRCA1 as BRCA1-C component is important for MRN/CTIP-dependent initiation of end-processing and therefore homology-directed DSBR [32], its incorporation into BRCA1-A complexes counterbalances these processes [74]. Germline variants were detected using freebayes (https://github.com/freebayes/freebayes). Variants were annotated with Ensembl’s VEP [75] and custom in-house data from previously sequenced patients. Variants were classified according to the ACMG guidelines [76].

Lymphoblastoid cell lines (LCLs)

LCLs were generated as previously described [57] and used at passage numbers 6–25 for functional analyses. LCL BR-0968 from a previous study was included as representative external healthy wild-type control [31]. Previously described LCLs [34], namely HA238 with heterozygously mutated BRCA2 (provided by Medical University Hannover, Germany), GM13023A with biallelic BRCA2/FANCD1-mutation (purchased at Coriell Institute, Camden, NJ, USA) and TK6 (provided by Eppendorf University Clinic, Hamburg, Germany) were further engaged for comparative analysis of cell viabilities. LCLs were cultured in RPMI 1640 medium (Gibco/Invitrogen, Carlsbad CA, USA) supplemented with 15% fetal bovine serum (Biochrom, Merck Millipore, Darmstadt, Germany) and antibiotics (Penicillin-Streptomycin-Glutamine, Gibco/Invitrogen). Experiments were performed in antibiotics-free media with 1.5% l-glutamine (Gibco/Invitrogen). LCLs and all other cell lines were tested negative for Mycoplasma contamination.

CRISPR/Cas9-mediated knockout of ABRAXAS1 in mammary epithelial cells

Parental MCF10A cells (ATCC®CRL-10317TM) used for the gene-editing were purchased from Sigma-Aldrich (Saint Louis, MO, USA) and were maintained according to the original protocol by Debnath and co-workers [77]. For experiments, cultivation relied on DMEM HAM’s F12 (PAA Laboratories GmbH, Pasching, Austria) with 5% horse serum (Gibco), MEM non-essential amino acids, 2 mM L-glutamine, 20 ng/ml EGF, 10 μg/ml Insulin, 100 ng/ml cholera toxin and 500 nM hydrocortisone.

In order to generate ABRAXAS1 KO cell lines the method of Ran and coworkers [78] was followed. Briefly, the protospacer pair (5′-CACCGCTGAGGCGGCGGTAGCATGG-3′ and 5′-AAACCCATGCTACCGCCGCCTCAGC-3′) targeting the translation initiation codon of ABRAXAS1 was first introduced into the BbsI site in the pCAG-eCas9-GFP-U6-gRNA vector that was a gift from Jizhong Zou (Addgene plasmid #79145; https://n2t.net/addgene:79145; RRID:Addgene_79145). The vector construct and empty vector were transfected into parental MCF10A cells using Nucleofector II device with a kit L and program X-001 (Lonza, Basel, Switzerland) to create ABRAXAS1-KO and control cell lines, respectively. After 48 h, GFP positive cells were sorted with BD FACSAriaTM III (BD Biosciences, San Jose, CA, USA) and single cell colonies were expanded and screened. Genomic DNA was purified with Epicentre’s QuickExtract solution (Illumina, Madison, WI, USA) from each cell colony, followed by the amplification and sequencing of the target area with the primers 5′-CAGCAGAAGCGAAGGAGGAG-3′ (forward) and 5′-CAGCAGAAGCGAAGGAGGAG-3′ (reverse). Several cell clones with a disrupted ATG codon were obtained and the clones ABRAXAS1-KO-D1 (D1) and ABRAXAS1-KO-E7 (E7) as well as control cell line ABRAXAS1-CTRL-A9 (Supplementary Fig. S8a) were selected for further analyses. Passage-matched isogenic cell lines were used in each experiment.

ABRAXAS1 expression plasmid and site-directed mutagenesis

Wild-type ABRAXAS1 carrying an N-terminal HA/FLAG-tag was cloned from pOZ-N-ABRAXAS1 vectors into pcDNA3.1/Hygro(-) as previously described [57]. To generate expression plasmids for ABRAXAS1 c.1106dup and ABRAXAS1 c.577C>T encoding ABRAXAS1 p.(Ser370Ilefs*2) and ABRAXAS1 p.(Arg193*), respectively, the QuikChange Lightning Site-Directed Mutagenesis Kit (Agilent Technologies, Waldbronn, Germany) was applied according to the manufacturer’s instructions. The ABRAXAS1 expression plasmid (pcDNA3.1-ABRAXAS1) was used as plasmid DNA template after isolation from a DAM methylase positive Escherichia coli strain. Primers containing the desired mutations were: 5′-GTTAGATACACAAGACAAACGGATCTAAAGCAGATACTGGTAG-3′ (forward) and 5′-CTACCAGTATCTGCTTTAGATCCGTTTGTCTTGTGTATCTAAC-3′ (reverse) for pcDNA3.1-ABRAXAS1 c.1106dup and 5′-TGTCCACTGGTTTTAGCTGAGCAGTACAAACACAC-3′ (forward) and 5´-GTGTGTTTGTACTGCTCAGCTAAAACCAGTGGACA-3′ (reverse) for pcDNA3.1-ABRAXAS1 c.577C>T, which were purchased from Eurofins MWG Synthesis GmbH (Ebersberg, Germany) or from Biomers (Ulm, Germany).

DSBR-pathway analysis

Determination of DSBR-frequencies in LCLs followed the protocol established in [31] including guidelines and quality controls. Briefly, plasmid DNA mixtures of 30 μl containing 10 μg of one of the DSBR substrates (HR-EGFP/5′EGFP for HR, EJ5SceGFP for NHEJ, EJ-EGFP for microhomology-mediated end-joining (MMEJ), 5′EGFP/HR-EGFP for SSA) [79, 80] together with 10 μg of the meganuclease expression plasmid pCMV-I-SceI and 10 μg of the filler plasmid pBS (pBlueScriptII KS; Stratagene, Heidelberg, Germany) were transfected into 2–4 × 106 LCL cells using electroporation cuvettes and a Gene Pulser with Pulse Controller (Bio-Rad Laboratories, München, Germany) at 200 V and 1050 μF (Bio-Rad). Subsequently, the transfected cells were transferred into fresh medium without antibiotics and cultivated for 48 h. Reconstitution of wild-type enhanced green fluorescent protein (EGFP) was determined by FACS analysis of the fraction of green fluorescent cells identified by gating in the FL1/FL2 dot plots (laser excitation at 488 nm) within the life cell-population in the side scatter/forward scatter dot plots (SSC/FSC gate) (FACS Calibur FACScan, BD BioSciences, Heidelberg, Germany). To determine transfection efficiencies, wild-type EGFP expression plasmid was used instead of the filler plasmid pBS in split samples each. Therefore, each quantification of green fluorescent cells monitoring DSBR was normalized using the individually determined transfection efficiency to calculate the DSBR-frequency.

To measure DSBR-frequencies in the chromatin context, K562 leukemia cells with chromosomally integrated reporter substrate HR-EGFP/3′EGFP, i.e. K562(HR-EGFP/3′EGFP) cells [80], were subjected to electroporation with 10 μg pCMV-I-SceI and 40 μg expression plasmid for one of the ABRAXAS1 variants each. DSBR-frequencies were measured 72 h after transfection by FACS.

Transfection of LCLs and MCF10A cells for expression of exogenous ABRAXAS1 variants

For additional DSBR measurements, immunofluorescence microscopy and PLA LCLs were (co-)electroporated with 40 μg of expression plasmid for wild-type ABRAXAS1, the variants c.1106dup or c.577C>T or empty vector pcDNA3.1/Hygro(-) and cultivated for 24 or 48 h. For DNA fiber and cell cycle assays, western blotting and RT-qPCR, we used the nucleofection protocol with Amaxa B cell Nucleofector Solution (Lonza, Basel, Switzerland) for introduction of 10 μg expression plasmid for one of the ABRAXAS1 variants.

For immunofluorescence microscopy, cell cycle and western blot analysis, MCF10A parental cells and clonal derivatives were nucleofected with 10 μg of expression plasmid for each ABRAXAS1 or control plasmid using Cell Line Nucleofector kit V using nucleofector program T-024 (Amaxa/Lonza) and cultivated for 24 h.

Immunofluorescence microscopy and proximity ligation assay (PLA)

For in situ analysis of DSBR cells were exposed to 2 Gy of ionizing radiation (Cs-137, GSR D1, Gamma-Service Medical GmbH, Leipzig, Germany), re-cultivated in fresh medium for 2 h (MCF10A clones) or 4 h with harvest by cytospinning on slides covered by poly-L-Lysine (Sigma-Aldrich, Steinheim, Germany) (LCLs). Depending on the specific antibody applied cells were pre-extracted or directly fixed with 3.7% formaldehyde and permeabilized with 0.5% TritionX-100. Five percent Goat Serum (Invitrogen) in PBS was utilized for blocking. Primary antibodies used were rabbit polyclonal antibodies targeting 53BP1 (NB100-304, Novus Biologicals, Littleton, CO, USA), MRE11 (NB100-142, Novus Biologicals) and RAD51 (H-92, Santa Cruz Biotechnology, Heidelberg, Germany) as well as mAbs against ABRAXAS1 (rabbit mAb 139191, clone EPR6310, Abcam, Cambridge, UK, recognizing the C-terminal fragment aa 394–408), BRCA1 (mouse mAb, clone MS110, Calbiochem, Darmstadt, Germany), γH2AX (mouse mAb, Ser139, clone JBW301, Millipore, Billerica, MA, USA) and p34 subunit of RPA (mouse mAb, clone 34–19, Calbiochem, Darmstadt, Germany). Secondary antibodies were AlexaFluor488- and AlexaFluor555-labeled from Invitrogen, Karlsruhe, Germany. Immunostained cells were embedded in VectaShield mounting media containing DAPI (4′,6-Diamidino-2-phenylindole dihydrochloride, Vector laboratories, Burlingame, CA, USA). In controls for simultaneous stainings with two primary antibodies cells were stained with each primary antibody together with the secondary antibody of the other primary antibody. For PLA Duolink® PLA Reagents (Sigma) were used according to the manufacturer’s instructions and engaging primary anti-ABRAXAS1, anti-MRE11 and anti-BRCA1 antibodies. For each experiment negative controls were analyzed, i.e. without the primary antibodies or without the PLA probes. Nuclear immunofluorescence signals were imaged with the Keyence BZ-9000 microscope (Keyence, Neu-Isenburg, Germany) using a 100× objective and applying the same exposure times as well as intensity and minimal focus size thresholds throughout one experimental set. Automated identification and quantification of foci were carried out using BZ-II Analyzer software.

DNA fiber spreading assay

Fourty-eight hours after transfection of the control LCL BR-0968 with expression plasmids for different ABRAXAS1 variants, we labeled cells with 20 µM 5-chloro-2-deoxyuridine (CldU, Sigma-Aldrich) for 30 min, followed by centrifugation and incubation in medium without (mock) or with 0.5 mM hydroxyurea (HU, Sigma-Aldrich) for 30 min essentially as described [35]. Hydroxyurea containing medium was again removed by centrifugation followed by incubation with 200 µM 5-Iodo-2 deoxyuridine (IdU, Sigma-Aldrich) for 30 min. Subsequently, cells were harvested, spotted, lysed, fixed and stained for immunofluorescence microscopy using the following primary antibodies: anti-BrdU (mouse, mAb, clone B44, 347580, BD BioScience) for detection of IdU and anti-BrdU (rat, mAb, clone BU1/75 [ICR1] NB500-169, Novus) for detection of CldU after blocking with 5% BSA. As secondary antibodies we used AlexaFluor555 (anti-mouse) and AlexaFluor488 (anti-rat) from Invitrogen (Darmstadt, Germany). The length of DNA fiber tracks was measured with a Keyence BZ-9000 microscope and BZ-II Analyser software (Keyence Germany GmbH, Neu-Isenburg, Germany).

Cellular survival and cell cycle distribution

For assessment of cell viabilities, LCLs were treated with different concentrations from 1 μM-2 mM of the PARP-inhibitor 1,5-isoquinolinediol (IQD) for 6 days and the colorimetric MTT assay was performed as described [31]. Media were replaced with fresh media including the corresponding IQD concentrations every second day. Each data set was corrected for mock-treatment. Cell viability curves were plotted and IC50-values of individual cell lines and cohorts were calculated using GraphPadPrism software.

To analyze the distribution of cells in cell-cycle phases and quantification of dying cells with subG1-content, cells were collected by centrifugation (LCLs) or trypsinized (MCF10A derivatives 24 h post transfection), washed with PBS, resuspended with 0.5 ml PBS and gently fixed on ice (1:1-mixture of acetone and 80% ethanol; −20 °C). Fixed cells were washed twice with ice-cold PBS, resuspended in propidium iodide staining solution (freshly added 50 µg/ml RNAse A; 50 µg/ml propidium iodide from Sigma-Aldrich in PBS) and incubated for 30 min in the dark. After diluting the suspension with 100 ml PBS with 0.2% EDTA, the stained cells were analyzed in a FACS Calibur flow cytometer (BD Biosciences).

Western blotting experiments

For the detection of endogenous proteins in LCLs, cells were harvested by centrifugation, whole cellular lysates prepared, 20–80 μg of proteins electrophoresed by SDS-PAGE and transferred to PVDF membrane as described [31]. For detection of exogenous proteins in MCF10A parental cells and clonal derivatives immunoblotting was performed 24 h post transfection with ABRAXAS1 expression plasmids and 24 µg of proteins subjected to immunoblotting. Proteins were detected by the following primary antibodies recognizing ABRAXAS1 (rabbit mAb 139191, clone EPR6310, Abcam, recognizing the C-terminal fragment aa 394–408), BRCA1 (mouse mAb, clone MS110, Calbiochem), phospho-Ser33 RPA32 (rabbit pAb, A300-244A, Bethyl, Montgomery, TX, USA), RPA32 antibody (rabbit pAb, A300-246A, Bethyl), Anti-phospho KAP1 Ser824 (rabbit pAb, A300-767A, Bethyl), Anti-KAP1 (rabbit pAb, A300-275A, Bethyl), cleaved PARP1 (rabbit pAb, AB3620, Chemicon/Millipore, Darmstadt, Germany), GAPDH (mouse mAb, clone T9484, Abcam), α-Tubulin (mouse mAb, clone DM1A, Abcam), and HA-tag (mouse mAb 2367, clone 6E2, Cell Signaling Technology, Danvers, MA, USA). Secondary antibodies were horseradish peroxidase-labelled goat anti-mouse and goat anti-rabbit (Rockland, San Diego, CA, USA). Chemiluminescent signals of band intensities were visualized by ClarityTM Western ECL Substrate (Bio-Rad Laboratories), quantified in the linear range following background signal subtraction and normalized to the corresponding loading controls (ChemiDocTM MP Imaging System and ImageLab Software 5.2.1, Bio-Rad).

Reverse transcription quantitative polymerase chain reaction (RT-qPCR)

To verify expression of exogenous ABRAXAS1 variants in LCLs we performed RT-qPCR analysis 48 h post transfection with expression plasmids. Total mRNA was isolated using the RNeasy Mini Kit (Qiagen, Hilden, Germany) and reverse-transcribed with QuantiTect Reverse Transcription Kit (Qiagen). Subsequent qPCR was performed using a SensiFast Lo-Rox kit (Bioline, Luckenwalde; Germany) on a Viia7 RUO Thermocycler (Applied Biosystems, Foster City, CA, USA). HA-ABRAXAS1-specific mRNAs were detected using ABRAXAS HEX primers and probes from Biomers (Ulm, Germany; Sense primer: 5′-CAAGCTCGATGGAGGATA-3′, antisense primer: 5′-TTCCCCAAGAAGAAAACC-3′ and probe: 5′-CCTACGACGTGCCCGACTAC-3′). RPS17 FAM primer assay from Bio-Rad and TBP VIC primer assay from Perkin Elmer (Thermo Fisher Scientific Inc., Waltham, Massachusetts, MA, USA) were used as internal controls. The differences in target mRNA expression were calculated with the 2− ΔΔCt method, whereby corrections were made for the mean of both housekee** genes RPS17 and TBP.

To detect CRISPR/Cas9-mediated ABRAXAS1 expression changes in MCF10A clones we performed RT-qPCR as above engaging qPCR primers from Biomers (Ulm, Germany) specific for exon 1 in ABRAXAS1, namely sense primer Abraxas Ex1-forward: 5′-CATGGAGGGGGAGAGTACGTC-3 (covering the CRISPR/Cas9 targeted start codon, underlined), antisense primer Abraxas Ex1-reverse: 5′-GTGTCCGAGTCCGTGTTGAG-3′ and probe Abraxas Ex1 Fam: 5′-CTCGGGCTTTGTGCTCGGCGCACT-3′. HSP90 and TBP VIC primer assays from Perkin Elmer (Thermo Fisher Scientific Inc., Waltham, Massachusetts, MA, USA) were used as internal controls.

Statistical analyses

Statistically significant differences between mean values of DSBR-frequencies, nuclear foci scores, track lengths in nascent DNA synthesis or cell cycle-phase percentages were calculated using the software GraphPad Prism versions 8–9 (GraphPad, San Diego, CA, USA). Once statistical significance was established for a data set by Kruskal–Wallis test, non-parametric Mann–Whitney test for unpaired samples was applied. GraphPad Prism versions 8–9 was also used to generate cell viability curves, calculate IC50 values and statistical significances of the differences between the IC50-values by Extra sum-of-squares F test of Log IC50. *P < 0.05; **P < 0.01; ***P < 0.001; ****P < 0.0001.