Skip to main content

Is BRD7 associated with spermatogenesis impairment and male infertility in humans? A case-control study in a Han Chinese population



Bromodomain-containing protein 7 (BRD7), a member of the bromodomain-containing protein family, plays important roles in chromatin modification and transcriptional regulation. A recent model of Brd7-knockout mice presented azoospermia and male infertility, implying the potential role of BRD7 in spermatogenic failure in humans. This case-control study aimed to explore the association of the BRD7 gene with spermatogenic efficiency and the risk of spermatogenic defects in humans.


A total of six heterozygous variants were detected in the coding and splicing regions of the BRD7 gene in patients with azoospermia. For each of four rare variants predicted to potentially damage BRD7 function, we further identified these four variants in oligozoospermia and normozoospermia as well. However, no difference in the allele and genotype frequencies of rare variants were observed between cases with spermatogenic failure and controls with normozoospermia; the sperm products of variant carriers were similar to those of noncarriers. Moreover, similar distribution of the alleles, genotypes and haplotypes of seven tag single nucleotide polymorphisms (tagSNPs) was observed between the cases with azoospermia and oligozoospermia and controls with normozoospermia; associations of tagSNP-distinguished BRD7 alleles with sperm products were not identified.


The lack of an association of BRD7-linked rare and common variants with spermatogenic failure implied a limited contribution of the BRD7 gene to spermatogenic efficiency and susceptibility to male infertility in humans.



Le bromodomaine contenant la protéine 7 (BRD7), un membre de la famille du bromodomaine contenant des protéines, joue des rôles importants dans la modification de la chromatine et la régulation transcriptionnelle. Un modèle récent de souris Brd7-knockout présentait une azoospermie et une infertilité mâle, ce qui implique un rôle potentiel de BRD7 dans l’altération de la spermatogenèse chez l’homme. Cette étude cas-témoins visait à explorer l’association du gène BRD7 avec l’efficacité de la spermatogenèse et le risque d’altérations spermatogéniques chez l’homme.


Un total de six variants hétérozygotes ont été détectés dans les régions de codage et d’épissage du gène BRD7 chez les patients présentant une azoospermie. Pour chacun des quatre variants rares prédits pour potentiellement endommager la fonction BRD7, nous avons en outre identifié ces quatre variants dans l’oligozoospermie et la normozoospermie. Cependant, nous n’avons observé aucune différence dans les fréquences d’allèle et de génotype des variants rares entre les cas avec altérations de la spermatogenèse et les témoins avec normozoospermie ; les produits du sperme des porteurs de variants étaient semblables à ceux des non-porteurs. Par ailleurs, on a observé une distribution semblable des allèles, des génotypes et des haplotypes de sept polymorphismes simples de nucléotide de balise (tagSNPs) entre les cas avec azoospermie ou oligozoospermie et les témoins normozoospermiques; aucune association n’a pas été identifiée entre les allèles BRD7 tagSNP-distingués et des produits du sperme.


L’absence d’association des variants rares liés à BRD7 et des variants communs liés à BRD7 avec les altérations de la spermatogenèse implique une contribution limitée du gène BRD7 à l’efficacité spermatogénique et à la susceptibilité à l’infertilité masculine chez l’homme.


Infertility has been a major global public health issue and causes significant psychosocial stress for couples suffering from this condition [1]. It is estimated that approximately 15% of couples suffer from infertility worldwide, and approximately half of infertility cases are caused by male factors [2]. Male infertility due to oligozoospermia (OZ) and azoospermia (AZ) is a common and complex disease. It has been postulated that the cause of infertility in 10–15% of infertile patients with AZ and severe OZ involves genetic factors, and the relevance of genetic anomalies gradually increases with decreasing sperm count [3, 4]. Both chromosomal abnormalities and monogenic mutations could be directly responsible for spermatogenic failure, in which Klinefelter’s syndrome and azoospermia factor (AZF) microdeletion are the most common cytogenetic and molecular genetic causes of spermatogenic failure, respectively [3]. However, the aetiology of approximately 40% of males with spermatogenic failure remains elusive [4], suggesting the significance of further exploring genetic causes of the protein 7 (BRD7), a member of the bromodomain-containing protein family, is highly conserved during evolution and ubiquitously distributed in various tissues with high expression in the testes of humans [5]. A recent study reported Brd7 knockout, causing AZ, and complete arrest of spermatogenesis at step 13 in mice [6]. Compared with BRD7+/+ mice, BRD7−/− mice showed a decrease in testicular size and seminiferous tubule diameter [6]. Furthermore, BRD7−/− mice had morphologically abnormal round spermatids, elongating spermatids and denatured condensed spermatids with irregular head shapes and deformed acrosomes [6]. Remarkably, BRD7 expression in the testis was reduced significantly in patients with idiopathic AZ relative to men with normozoospermia (NZ) [6]. These findings suggest a vital role of the BRD7 gene in spermatogenesis. In this case, it would be interesting to determine whether the BRD7 gene is associated with the risk of spermatogenic failure and male infertility in humans. In the present study, we detected rare and common variants of BRD7 in 315 infertile patients with spermatogenic failure and 995 men with NZ. Our results implied a limited contribution of the BRD7 gene to susceptibility to spermatogenic failure and male infertility in humans.

Materials and methods


The sample size for the case-control study was calculated using QUANTO1.2 software (Jim Gauderman and John Morrison, USA). The parameters of the type I error rate and statistical power were set at 0.05 and 0.80, respectively. The evaluated sample size was at least 314 for the case group when the size ratio of the patients and controls was 1:3. According to the sample size, we recruited 315 unrelated infertile men with idiopathic spermatogenesis impairment and 995 normozoospermic men (couple infertility due to female factors) from two affiliated hospitals of Sichuan University and Chengdu Women’s and Children’s Central Hospital between 2015 and 2020.

The diagnosis of all patients was based on standard clinical procedures, including history and physical examination, semen analysis, serum hormone analysis, ultrasound evaluation and genetic testing [7]. All of the participants underwent at least two semen analyses. Based on World Health Organization guidelines [8], AZ is defined when no sperm is found under the microscope after the semen is centrifuged (3000×g) for 15 min. OZ is defined as sperm concentration (SC) < 15 × 106/ml and total sperm count (TSC) < 39 × 106/ejaculate. NZ is defined as SC > 15 × 106/ml, TSC > 39 × 106/ejaculate and normal sperm motility and morphology. Serum hormones, including follicle-stimulating hormone (FSH), luteinizing hormone (LH) and testosterone (T), were detected in individuals. Patients with alcohol or drug abuse, karyotype abnormalities, AZF microdeletions, hypogonadotrophic hypogonadism, cryptorchidism, varicocele, seminal ductal obstruction, testicular trauma and tumours were excluded based on evaluation with standard clinical procedures. The case group included 142 patients with nonobstructive azoospermia (NOA) and 173 patients with OZ aged 26 to 46 years. The patients with NOA included 51 with hypospermatogenesis (8 ~ 9 scores), 30 with spermatid arrest (6 ~ 7 scores), 22 with spermatocyte arrest (4 ~ 5 scores), 16 with spermatogonia arrest (3 scores), and 23 with Sertoli cell-only syndrome (2 scores) according to the Johnsen score and predominant histopathologic pattern [9]. The controls with NZ ranged in age from 22 to 45 years old. The semen and hormonal parameters of the subjects are shown in Table 1. This study was approved by the Biomedical Research Ethics Committee of West China Hospital, Sichuan University (No. 783), and written informed consent was obtained from each participant.

Table 1 The basic characteristics of the study subjects

Detection of rare variants in the coding region and splice site of BRD7

Genomic DNA was collected from whole blood using a Blood DNA Purification Kit (BioTeke, China). The quality and concentration of DNA samples were assessed by 1% agarose gel electrophoresis. For the 142 patients with NOA, all seventeen exons of BRD7 (NG_023418) including splice sites were amplified by polymerase chain reaction (PCR), and the PCR primer information is shown in Supplementary table 1. Sanger sequencing of the PCR product was performed on a 3700XL System (Applied Biosystems, USA).

Detected variants with a minor allele frequency (MAF) < 1% in the Genome Aggregation Database (gnomAD) [10] and 1000 Genomes Project [11] were classified as ‘rare variants’. Among these variants, the influence of a missense variant on gene function was predicted by three in silico algorithms, including SIFT [12], PolyPhen-2 [13] and Mutation Taster [14], and the influence of synonymous variants and a variant in splice site on RNA splicing was predicted by two in silico algorithms, including MaxEntScan [15] and Human Splicing Finder [16]. For the rare variants predicted to potentially damage the function of BRD7 by at least two of three algorithms (SIFT, PolyPhen-2 and Mutation Taster) or one of two algorithms (MaxEntScan and Human Splicing Finder), further genotyping was conducted in 173 infertile males with OZ and 995 controls with NZ by Sanger sequencing.

Genotyping of the common variants in BRD7

The genotypes of single nucleotide polymorphisms (SNPs) within 10 kb are usually associated with the same or similar effects [17, 18], and a single tagSNP could represent the information of more SNPs in the region. Currently, tagSNP selection is mostly based on linkage disequilibrium (LD) [19]. LD, a nonrandom association of alleles at a pair of loci, is quantified by the value of D′ or r2 [17, 20]. The value of r2 is directly related to the statistical power of detecting unassayed loci and disease-associated polymorphisms [17]. When the value of r2 ≥ 0.8, two loci are regarded as exhibiting a strong LD [19]. In the present study, we extracted BRD7 genotype data from 2 kb upstream of the transcription start site to 2 kb downstream of the transcription stop site from the 1000 Genomes Project database. The tagSNPs were screened and evaluated using Haploview 4.2 software (Broad Institute of MIT and Harvard, USA). Based on the data of Han Chinese individuals in Beijing, a total of seven tagSNPs, rs7196135, rs117164075, rs76946718, rs1062348, rs79483509, rs62029995 and rs11644238, were eventually selected with MAF > 5% and LD value of r2 ≥ 0. 8. In theory, these tagSNPs could capture greater than 90% of the targeted BRD7 alleles at an r2 threshold of 0.8.

Genotyping of the tagSNPs was performed for 315 infertile patients with impaired spermatogenesis and 995 controls with NZ using a SNPscan™ Kit (Genesky Biotechnologies, China). As described previously [21], the genotypes of the tagSNPs were identified by double-ligation and multiplex fluorescence PCR, and the results were analysed using GeneMapper 4.1 software (Applied Biosystems, USA). For quality control, 10% of the total samples were randomly selected for the second test with a concordance rate of 100%. Moreover, 5% of the samples were confirmed to have tagSNP genotypes by Sanger sequencing, producing 100% identity.

Statistical analysis

The distribution of semen parameters, including SC, TSC and motility, was analysed using the Kolmogorov-Smirnov test or descriptive statistical index in SPSS 17.0 software (SPSS Inc., USA). The Hardy-Weinberg equilibrium (HWE) test was performed for each tagSNP using PLINK 1.9 software (Shaun Purcell, USA). The genotype distributions and allele frequencies of the rare variants and tagSNPs were compared between patients and controls using Pearson’s χ2 test or Fisher’s exact test in SPSS 17.0 software. LD analysis of the tagSNPs was conducted using Haploview 4.2 software. Haplotype analysis of the tagSNPs was performed using SHEsis software [22]. The Mann-Whitney U or Kruskal-Wallis test was performed to compare the distribution differences of SC and TSC among different genotypes of patients with OZ and fertile men. Continuous variables are presented as the mean ± standard deviation of the mean (mean ± SD) or median and interquartile range, and categorical variables are presented as frequencies (%). For all statistical tests, P < 0.05 was considered to be statistically significant. In addition, the Bonferroni method was applied to adjust for multiple testing by dividing the critical level of significance by the number of comparisons.


First, we detected variants in the coding region and splice site of BRD7 in 142 patients with NOA. As a result, a total of six exonic and splicing variants were classified as heterozygous (Table 2). The properties of these variants were evaluated with publicly available population databases and in silico tools. After excluding one synonymous variant (rs201820448) without supporting evidence for its influence on RNA splicing and another (rs1062348) with MAF > 1% in the East Asian population of 1000 Genomes and gnomAD databases, the remaining four rare variants (Supplementary Fig. 1), including rs116422109, rs202057136, rs115302634 and rs188183810, were further subjected to genotyping by Sanger sequencing in 173 infertile males with OZ and 995 normozoospermic men. The four rare variants were also found in the heterozygous state in 173 patients with OZ and 995 controls. The genotype distributions of these variants were in accordance with HWE in both the patient and control groups (Supplementary Table 2). Our results showed a similar distribution of alleles and genotypes of these variants between 995 controls and 315 infertile patients (142 with NOA and 173 with OZ) (Table 3). The human BRD7 gene is mainly expressed in the nuclei of primary spermatocytes and round spermatids [6], implying that the impaired function of BRD7 may cause spermatocyte or spermatid arrest. Thus, we further compared the distribution of alleles and genotypes between the controls with NZ and NOA patients with either of the two pathological phenotypes in the testis. However, we failed to identify any significant difference in the distributions of alleles and genotypes of these variants between the two groups (Table 3). Further comparison did not reveal any difference in the sperm products between carriers of the variants and noncarriers (Table 4).

Table 2 The bioinformatics analysis of exonic and splicing variants detected in 142 patients with AZ
Table 3 Comparison of allele and genotype frequencies of the rare variants between patients with OZ or AZ and controls with NZ
Table 4 Comparison of sperm products among different genotypes of the rare variants

To further explore the association of the common variants of BRD7 with spermatogenesis failure, we identified seven BRD7-linked tagSNPs and performed genotyping in 315 patients with NOA or OZ and 995 controls with NZ. The genotype distributions of the seven common SNPs were in accordance with HWE in both the patient and control groups (Supplementary table 3), suggesting that the study sample is representative of the population. As shown in Table 5, the distribution of alleles and genotypes of the seven tagSNPs was similar between patients with NOA or OZ and fertile male controls.

Table 5 Comparison of allele and genotype frequencies of the tagSNPs between patients with OZ or AZ and controls with NZ

Typically, a haplotype composed of SNPs may lead to a larger joint effect on complex traits compared with that noted for single-marker analysis [23]. Therefore, we next conducted pairwise LD analysis of the tagSNPs using Haploview 4.2 software. The results showed that five of the seven tagSNPs, rs62029995, rs76946718, rs79483509, rs1062348 and rs117164075, formed a haploid block that exhibited a strong LD in both patients and controls (Fig. 1). Haplotype analysis with SHEsis software predicted six haplotypes of the haploid block with a frequency of greater than 0.03. However, we did not identify any significant difference in the distribution of these haplotypes between patients with spermatogenesis failure and controls with NZ (Table 6).

Fig. 1

The linkage disequilibrium (LD) pattern of seven BRD7-linked tagSNPs in the azoospermia, oligozoospermia and control groups. Legend: Five of the seven tagSNPs, rs62029995, rs76946718, rs79483509, rs1062348 and rs117164075, formed a haploid block with strong linkage disequilibrium in both groups of patients and the controls. LD was evaluated with D’ values. a Control group with normozoospermia; b Oligozoospermia group; c Azoospermia group

Table 6 Comparison of the haplotype frequencies between patients with OZ or AZ and controls with NZ

Furthermore, we investigated the correlation between BRD7 and sperm products, including SC and TSC. The results showed that men with any BRD7 alleles distinguished by the seven tagSNPs presented similar SC and TSC (Table 7), further implying the absence of the association of BRD7 tagSNPs with susceptibility to spermatogenic failure.

Table 7 Comparison of sperm products among different genotypes of tagSNPs


Spermatogenesis is a complex process involving approximately 2000 genes [4, 24]. By studying human patients with spermatogenic failure, some autosome-linked gene variants have been demonstrated to cause central hypogonadism, monomorphic teratozoospermia or asthenospermia [4]. In recent years, the reproductive investigation of gene-knockout mice has suggested more candidate genes for spermatogenic failure [25], providing an additional clue for the aetiological study of spermatogenic failure in humans. In this case, it is encouraged to clarify the contribution of these genes to spermatogenic failure and male infertility in humans when considering the similarity of function between mouse and human genes [26].

BRD7 plays various roles in cellular biological processes, such as transcriptional regulation, chromatin modification and cell cycle control [27,28,29]. As a catalytic subunit of the switch/sucrose nonfermenting (SWI/SNF) complex, brahma-related gene 1 (BRG1) facilitates DNA double-strand break repair and recombination during meiosis in the male germline [30], and BRD7 is a subunit of polybromo-associated BRG1-associated factor-specific SWI/SNF and is essential for the activation and repression of target genes in embryonic stem cells [31]. In addition, as a protein recognition module, the bromodomain can bind acetyllysine residues on the histone tail, which is a pivotal mark of epigenetic regulation [32, 33]. Remarkably, BRD7 is highly expressed in the pachytene stage to the round spermatid stage during mouse spermatogenesis, which is similar to that in humans, and Brd7−/− male mice present AZ and male infertility [6]. Interestingly, a study reported that whole-body BRD7 knockout in mice caused embryonic lethality at mid-gestation, suggesting a pivotal role for BRD7 during growth and development [34]. This discrepancy between the two studies was probably due to the different knockout systems. The former BRD7-knockout mice were obtained using the Cre/loxP and flp/FRT recombination systems, which both conditionally and globally destroyed BRD7 [6]. In the Cre/loxP system, Cre expression is controlled by the EII α promoter, and minor leakage of the Cre/EII α promoter may lead to low BRD7 expression that is sufficient to allow knockout mice to survive and cause male infertility [35, 36]. Moreover, another bromodomain protein, bromodomain testis-specific protein (BRDT), has been reported to be involved in susceptibility to spermatogenesis impairment in humans [37]. These findings imply that BRD7 may be a potential candidate gene for human spermatogenesis impairment.

To explore the association of BRD7 with human spermatogenic failure, we comprehensively investigated the influence of rare and common variants of BRD7 on the spermatogenic phenotype in 315 infertile patients with AZ or OZ and 995 males with NZ in the present study. However, we did not identify any rare variants of BRD7 that could impair sperm production to influence the risk of spermatogenic failure in our population. Regarding the common variants of BRD7, we failed to obtain any evidence for the association of their alleles with spermatogenic efficiency and susceptibility to spermatogenic failure. Collectively, our findings imply a limited contribution of BRD7 to human male infertility. This observation may be reasonable when considering that BRD7 may have partial functional redundancy with other genes during spermatogenesis in humans; thus, it is potentially nonessential for spermatogenesis in humans [38, 39].

Several limitations of the present study should be noted: (i) Approximately 2000 genes play a role in spermatogenesis, and it is highly possible that only a small number of patients with AZ are likely to carry two pathogenic alleles of BRD7. These patients may not be detected in the limited number of AZ samples. Thus, the spermatogenic phenotype of complete loss of BRD7 function could not be assessed in humans. (ii) The detection of rare variants in patients with OZ was not performed, and the patients could carry different rare variants than those carried by patients with AZ. (iii) The selected tagSNPs captured 90% of the target alleles with r2 > 0.8 and MAF > 0.05, but they were not representative of all target alleles. (iv) Testicular BRD7 levels of patients with severe spermatogenic impairment were not assessed due to ethical reasons. Our results require further validation in a larger cohort considering the limited number of participants in this study.


In summary, this study is the first to investigate the association of the BRD7 gene with spermatogenic failure and male infertility in humans. We failed to obtain any rare or common variant-based evidence for the significant influence of BRD7 on spermatogenic efficiency and susceptibility in men, implying a limited contribution of the autosome-linked gene to spermatogenic failure and male infertility in humans.

Availability of data and materials

The datasets used and analysed during the current study are available from the corresponding author on reasonable request.



Bromodomain-containing protein 7


Single nucleotide polymorphisms


Azoospermia factor








Nonobstructive azoospermia


Sperm concentration


Total sperm count


Follicle-stimulating hormone


Luteinizing hormone




polymerase chain reaction


Genome Aggregation Database


Minor allele frequency


Hardy-Weinberg equilibrium


Linkage disequilibrium


Switch/sucrose nonfermenting


Brahma-related gene 1


Bromodomain testis-specific protein


  1. 1.

    Jaoul M, Bailly M, Albert M, Wainer R, Selva J, Boitrelle F. Identity suffering in infertile men. Basic Clin Androl. 2014;24(1):1.

    Article  PubMed  PubMed Central  Google Scholar 

  2. 2.

    Poongothai J, Gopenath TS, Manonayaki S. Genetics of human male infertility. Singap Med J. 2009;50(4):336–47.

    CAS  Google Scholar 

  3. 3.

    Asero P, Calogero AE, Condorelli RA, Mongioi L, Vicari E, Lanzafame F, et al. Relevance of genetic investigation in male infertility. J Endocrinol Investig. 2014;37(5):415–27.

    CAS  Article  Google Scholar 

  4. 4.

    Krausz C, Riera-Escamilla A. Genetics of male infertility. Nat Rev Urol. 2018;15(6):369–84.

    CAS  Article  PubMed  Google Scholar 

  5. 5.

    The Human Protein Atlas Database. Accessed 10 Sept 2019.

  6. 6.

    Wang H, Zhao R, Guo C, Jiang S, Yang J, Xu Y, et al. Knockout of BRD7 results in impaired spermatogenesis and male infertility. Sci Rep. 2016;6(1):21776.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  7. 7.

    Colpi GM, Francavilla S, Haidl G, Link K, Behre HM, Goulis DG, et al. European academy of andrology guideline management of oligo-astheno-teratozoospermia. Andrology. 2018;6(4):513–24.

    CAS  Article  PubMed  Google Scholar 

  8. 8.

    WHO. WHO laboratory manual for the examination and processing of human semen. 5th ed: World Heath Organisation; ss.

  9. 9.

    Johnsen SG. Testicular biopsy score count--a method for registration of spermatogenesis in human testes: normal values and results in 335 hypogonadal males. Hormones. 1970;1(1):2–25.

    CAS  Article  PubMed  Google Scholar 

  10. 10.

    Genome Aggregation Database. Accessed 10 Aug 2020.

  11. 11.

    1000 Genomes Project Database. Accessed 10 Aug 2020.

  12. 12.

    SIFT. Accessed 20 Aug 2020.

  13. 13.

    PolyPhen-2. Accessed 20 Aug 2020.

  14. 14.

    Mutation Taster. Accessed 20 Aug 2020.

  15. 15.

    MaxEntScan. Accessed 20 Aug 2020.

  16. 16.

    Human Splicing Finder. Accessed 20 Aug 2020.

  17. 17.

    Carlson CS, Eberle MA, Rieder MJ, Yi Q, Kruglyak L, Nickerson DA. Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium. Am J Hum Genet. 2004;74(1):106–20.

    CAS  Article  PubMed  Google Scholar 

  18. 18.

    Silesian AP, Szyda J. Population parameters incorporated into genome-wide tagSNP selection. Animal. 2013;7(8):1227–30.

    CAS  Article  PubMed  Google Scholar 

  19. 19.

    Liao B, Wang X, Zhu W, Li X, Cai L, Chen H. New multilocus linkage disequilibrium measure for tag SNP selection. J Bioinforma Comput Biol. 2017;15(1):1750001.

    CAS  Article  Google Scholar 

  20. 20.

    Jorde LB. Linkage disequilibrium and the search for complex disease genes. Genome Res. 2000;10(10):1435–44.

    CAS  Article  PubMed  Google Scholar 

  21. 21.

    Chen X, Li S, Yang Y, Yang X, Liu Y, Liu Y, et al. Genome-wide association study validation identifies novel loci for atherosclerotic cardiovascular disease. J Thromb Haemost. 2012;10(8):1508–14.

    CAS  Article  PubMed  Google Scholar 

  22. 22.

    SHEsis. Accessed 30 Oct 2020.

  23. 23.

    Liu N, Zhang K, Zhao H. Haplotype-association analysis. Adv Genet. 2008;60:335–405.

    Article  PubMed  Google Scholar 

  24. 24.

    Jan SZ, Vormer TL, Jongejan A, Roling MD, Silber SJ, de Rooij DG, et al. Unraveling transcriptome dynamics in human spermatogenesis. Development. 2017;144(20):3659–73.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  25. 25.

    Jamsai D, O'Bryan MK. Mouse models in male fertility research. Asian J Androl. 2011;13(1):139–51.

    Article  PubMed  Google Scholar 

  26. 26.

    Church DM, Goodstadt L, Hillier LW, Zody MC, Goldstein S, She X, et al. Lineage-specific biology revealed by a finished genome assembly of the mouse. PLoS Biol. 2009;7(5):e1000112.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  27. 27.

    Peng C, Zhou J, Liu HY, Zhou M, Wang LL, Zhang QH, et al. The transcriptional regulation role of BRD7 by binding to acetylated histone through bromodomain. J Cell Biochem. 2006;97(4):882–92.

    CAS  Article  PubMed  Google Scholar 

  28. 28.

    Peng C, Liu HY, Zhou M, Zhang LM, Li XL, Shen SR, et al. BRD7 suppresses the growth of nasopharyngeal carcinoma cells (HNE1) through negatively regulating beta-catenin and ERK pathways. Mol Cell Biochem. 2007;303(1–2):141–9.

    CAS  Article  PubMed  Google Scholar 

  29. 29.

    Yu X, Li Z, Shen J. BRD7: a novel tumor suppressor gene in different cancers. Am J Transl Res. 2016;8(2):742–8.

    CAS  PubMed  PubMed Central  Google Scholar 

  30. 30.

    Kim Y, Fedoriw AM, Magnuson T. An essential role for a mammalian SWI/SNF chromatin-remodeling complex during male meiosis. Development. 2012;139(6):1133–40.

    Article  PubMed  PubMed Central  Google Scholar 

  31. 31.

    Kaeser MD, Aslanian A, Dong MQ, Yates JR 3rd, Emerson BM. BRD7, a novel PBAF-specific SWI/SNF subunit, is required for target gene activation and repression in embryonic stem cells. J Biol Chem. 2008;283(47):32254–63.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  32. 32.

    Clark PG, Dixon DJ, Brennan PE. Development of chemical probes for the bromodomains of BRD7 and BRD9. Drug Discov Today Technol. 2016;19:73–80.

    Article  PubMed  Google Scholar 

  33. 33.

    Lloyd JT, Glass KC. Biological function and histone recognition of family IV bromodomain-containing proteins. J Cell Physiol. 2018;233(3):1877–86.

    CAS  Article  PubMed  Google Scholar 

  34. 34.

    Kim Y, Andres Salazar Hernandez M, Herrema H, Delibasi T, Park SW. The role of BRD7 in embryo development and glucose metabolism. J Cell Mol Med. 2016;20(8):1561–70.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  35. 35.

    Ye Q, Zheng Y, Fan S, Qin Z, Li N, Tang A, et al. Lactoferrin deficiency promotes colitis-associated colorectal dysplasia in mice. PLoS One. 2014;9(7):e103298.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  36. 36.

    Park SW, Lee JM. Emerging Roles of BRD7 in Pathophysiology. Int J Mol Sci. 2020;21:19.

    Google Scholar 

  37. 37.

    Plaseski T, Noveski P, Popeska Z, Efremov GD, Plaseska-Karanfilska D. Association study of single-nucleotide polymorphisms in FASLG, JMJDIA, LOC203413, TEX15, BRDT, OR2W3, INSR, and TAS2R38 genes with male infertility. J Androl. 2012;33(4):675–83.

    CAS  Article  PubMed  Google Scholar 

  38. 38.

    Liu H, Chen CH, Espinoza-Lewis RA, Jiao Z, Sheu I, Hu X, et al. Functional redundancy between human SHOX and mouse Shox2 genes in the regulation of sinoatrial node formation and pacemaking function. J Biol Chem. 2011;286(19):17029–38.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  39. 39.

    Nowak MA, Boerlijst MC, Cooke J, Smith JM. Evolution of genetic redundancy. Nature. 1997;388(6638):167–71.

    CAS  Article  PubMed  Google Scholar 

Download references


The authors thank the subjects who voluntarily participated in the study. The authors thank the participants of West China Hospital and West China Second Hospital, Sichuan University, Chengdu Women’s and Children’s Central Hospital for their clinical support of this work.


This study was funded by the National Natural Science Foundation of China (Grant Number: 81871203).

Author information




TRH, MHL, XYL, ZKW, YWZ, YQL, DCT, XYZ, XLT and YY contributed to conceptualization. TRH, MHL and XYL designed and performed the study. TRH and SYX contributed to software. TRH and MHL analysed the data. TRH and MHL contributed to writing-original draft. TRH and YY revised the manuscript. YY supervised the study and provided financial support. All authors have read and approved the final version of the manuscript.

Corresponding author

Correspondence to Yuan Yang.

Ethics declarations

Ethics approval and consent to participate

This study was approved by the Biomedical Research Ethics Committee of West China Hospital, Sichuan University (No. 783), and all subjects provided informed consent.

Consent for publication

Not applicable.

Competing interests

The authors declare no conflicts of interest.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Additional file 1: Figure S1.

Title: Sanger sequencing diagram of the rare variants. Legend: Sanger sequencing of rare variants predicted to potentially damage the function of bromodomain containing 7 (BRD7), including rs116422109, rs202057136, rs115302634 and rs188183810.

Additional file 2: Table S1.

Primers for PCR and sequencing of BRD7. Table S2. Testing for Hardy-Weinberg equilibrium of the rare variants. Table S3. Testing for Hardy-Weinberg equilibrium of the common variants.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

He, T., Liu, M., Tao, D. et al. Is BRD7 associated with spermatogenesis impairment and male infertility in humans? A case-control study in a Han Chinese population. Basic Clin. Androl. 31, 19 (2021).

Download citation


  • BRD7
  • Rare variant
  • tagSNP
  • Spermatogenic failure
  • Male infertility


  • BRD7
  • Variants rares
  • tagSNP
  • Altération de la spermatogenèse
  • Infertilité masculine.