• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

涉及 SRY 相关基因 SOX8 的突变与一系列人类生殖异常有关。

Mutations involving the SRY-related gene SOX8 are associated with a spectrum of human reproductive anomalies.

机构信息

APHP Département de Génétique Médicale, Hôpital Armand Trousseau, Paris 75012, France.

UPMC, University Paris 06, INSERM UMR_S933, Hôpital Armand Trousseau, Paris 75012, France.

出版信息

Hum Mol Genet. 2018 Apr 1;27(7):1228-1240. doi: 10.1093/hmg/ddy037.

DOI:10.1093/hmg/ddy037
PMID:29373757
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6159538/
Abstract

SOX8 is an HMG-box transcription factor closely related to SRY and SOX9. Deletion of the gene encoding Sox8 in mice causes reproductive dysfunction but the role of SOX8 in humans is unknown. Here, we show that SOX8 is expressed in the somatic cells of the early developing gonad in the human and influences human sex determination. We identified two individuals with 46, XY disorders/differences in sex development (DSD) and chromosomal rearrangements encompassing the SOX8 locus and a third individual with 46, XY DSD and a missense mutation in the HMG-box of SOX8. In vitro functional assays indicate that this mutation alters the biological activity of the protein. As an emerging body of evidence suggests that DSDs and infertility can have common etiologies, we also analysed SOX8 in a cohort of infertile men (n = 274) and two independent cohorts of women with primary ovarian insufficiency (POI; n = 153 and n = 104). SOX8 mutations were found at increased frequency in oligozoospermic men (3.5%; P < 0.05) and POI (5.06%; P = 4.5 × 10-5) as compared with fertile/normospermic control populations (0.74%). The mutant proteins identified altered SOX8 biological activity as compared with the wild-type protein. These data demonstrate that SOX8 plays an important role in human reproduction and SOX8 mutations contribute to a spectrum of phenotypes including 46, XY DSD, male infertility and 46, XX POI.

摘要

SOX8 是一种与 SRY 和 SOX9 密切相关的 HMG 盒转录因子。在小鼠中删除编码 Sox8 的基因会导致生殖功能障碍,但 SOX8 在人类中的作用尚不清楚。在这里,我们表明 SOX8 在人类早期发育性腺的体细胞中表达,并影响人类性别决定。我们鉴定了两名 46,XY 性别发育障碍/差异(DSD)和包含 SOX8 基因座的染色体重排的个体,以及第三名 46,XY DSD 和 SOX8 HMG 盒错义突变的个体。体外功能测定表明该突变改变了蛋白质的生物学活性。由于越来越多的证据表明 DSD 和不育可能有共同的病因,我们还在一组不育男性(n=274)和两组原发性卵巢功能不全(POI;n=153 和 n=104)的女性中分析了 SOX8。在少精子症男性(3.5%;P<0.05)和 POI(5.06%;P=4.5×10-5)中发现 SOX8 突变的频率增加,与生育/正常精子对照人群(0.74%)相比。鉴定出的突变蛋白与野生型蛋白相比改变了 SOX8 的生物学活性。这些数据表明 SOX8 在人类生殖中发挥重要作用,SOX8 突变导致包括 46,XY DSD、男性不育和 46,XX POI 在内的一系列表型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b8/6159538/8983e0439f2c/ddy037f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b8/6159538/d26f269699ef/ddy037f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b8/6159538/ae84a8fa7bc8/ddy037f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b8/6159538/f2af99e15f8f/ddy037f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b8/6159538/f92dcc8d8af9/ddy037f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b8/6159538/b5242c246e4d/ddy037f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b8/6159538/0209877b5433/ddy037f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b8/6159538/8983e0439f2c/ddy037f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b8/6159538/d26f269699ef/ddy037f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b8/6159538/ae84a8fa7bc8/ddy037f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b8/6159538/f2af99e15f8f/ddy037f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b8/6159538/f92dcc8d8af9/ddy037f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b8/6159538/b5242c246e4d/ddy037f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b8/6159538/0209877b5433/ddy037f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b8/6159538/8983e0439f2c/ddy037f7.jpg

相似文献

1
Mutations involving the SRY-related gene SOX8 are associated with a spectrum of human reproductive anomalies.涉及 SRY 相关基因 SOX8 的突变与一系列人类生殖异常有关。
Hum Mol Genet. 2018 Apr 1;27(7):1228-1240. doi: 10.1093/hmg/ddy037.
2
and act redundantly for ovarian-to-testicular fate reprogramming in the absence of in mouse sex reversals.并且在小鼠性别反转中, 在卵巢到睾丸命运重编程中发挥冗余作用。
Elife. 2020 May 26;9:e53972. doi: 10.7554/eLife.53972.
3
Variation analysis of SOX8 gene in Chinese men with non-obstructive azoospermia or oligozoospermia.SOX8 基因在中国男性非梗阻性无精子症或严重少精子症中的变异分析。
Andrologia. 2020 May;52(4):e13531. doi: 10.1111/and.13531. Epub 2020 Feb 12.
4
Ten novel mutations in the NR5A1 gene cause disordered sex development in 46,XY and ovarian insufficiency in 46,XX individuals.NR5A1 基因中的 10 个新突变导致 46,XY 个体的性别发育障碍和 46,XX 个体的卵巢功能不全。
J Clin Endocrinol Metab. 2012 Jul;97(7):E1294-306. doi: 10.1210/jc.2011-3169. Epub 2012 May 1.
5
MYRF haploinsufficiency causes 46,XY and 46,XX disorders of sex development: bioinformatics consideration.MYRF 杂合性缺失导致 46,XY 和 46,XX 性发育障碍:生物信息学考虑。
Hum Mol Genet. 2019 Jul 15;28(14):2319-2329. doi: 10.1093/hmg/ddz066.
6
A recurrent p.Arg92Trp variant in steroidogenic factor-1 (NR5A1) can act as a molecular switch in human sex development.类固醇生成因子1(NR5A1)中反复出现的p.Arg92Trp变异可作为人类性发育中的分子开关。
Hum Mol Genet. 2016 Aug 15;25(16):3446-3453. doi: 10.1093/hmg/ddw186. Epub 2016 Jul 4.
7
Additional evidence for the role of chromosomal imbalances and SOX8, ZNRF3 and HHAT gene variants in early human testis development. 额外证据表明染色体失衡以及 SOX8、ZNRF3 和 HHAT 基因变异在人类早期睾丸发育中的作用。
Reprod Biol Endocrinol. 2023 Jan 11;21(1):2. doi: 10.1186/s12958-022-01045-7.
8
Familial forms of disorders of sex development may be common if infertility is considered a comorbidity.如果将不孕症视为一种合并症,性发育障碍的家族性形式可能很常见。
BMC Pediatr. 2016 Nov 29;16(1):195. doi: 10.1186/s12887-016-0737-0.
9
Wide spectrum of NR5A1-related phenotypes in 46,XY and 46,XX individuals.46,XY和46,XX个体中与NR5A1相关的广泛表型谱。
Birth Defects Res C Embryo Today. 2016 Dec;108(4):309-320. doi: 10.1002/bdrc.21145.
10
The novel p.Cys65Tyr mutation in NR5A1 gene in three 46,XY siblings with normal testosterone levels and their mother with primary ovarian insufficiency.NR5A1 基因中新型 p.Cys65Tyr 突变导致三例 46,XY 表型兄弟及其原发性卵巢功能不全的母亲出现正常睾酮水平。
BMC Med Genet. 2014 Jan 10;15:7. doi: 10.1186/1471-2350-15-7.

引用本文的文献

1
The quality of human eggs and its pre-IVF incubation.人类卵子的质量及其体外受精前培养
Reprod Med Biol. 2025 May 2;24(1):e12652. doi: 10.1002/rmb2.12652. eCollection 2025 Jan-Dec.
2
Sox8: a multifaceted transcription factor in development and disease.Sox8:一种在发育和疾病中具有多方面作用的转录因子。
Biol Open. 2025 Feb 15;14(2). doi: 10.1242/bio.061840. Epub 2025 Feb 12.
3
Characterization of 35 Novel NR5A1/SF-1 Variants Identified in Individuals With Atypical Sexual Development: The SF1next Study.在具有非典型性发育个体中鉴定出的35种新型NR5A1/SF-1变异体的特征:SF1next研究

本文引用的文献

1
Deciphering Cell Lineage Specification during Male Sex Determination with Single-Cell RNA Sequencing.单细胞 RNA 测序解析雄性性别决定过程中的细胞谱系特化
Cell Rep. 2018 Feb 6;22(6):1589-1599. doi: 10.1016/j.celrep.2018.01.043.
2
Normal Levels of Sox9 Expression in the Developing Mouse Testis Depend on the TES/TESCO Enhancer, but This Does Not Act Alone.发育中小鼠睾丸中Sox9的正常表达水平依赖于TES/TESCO增强子,但这并非其单独作用。
PLoS Genet. 2017 Jan 3;13(1):e1006520. doi: 10.1371/journal.pgen.1006520. eCollection 2017 Jan.
3
A recurrent p.Arg92Trp variant in steroidogenic factor-1 (NR5A1) can act as a molecular switch in human sex development.
J Clin Endocrinol Metab. 2025 Feb 18;110(3):e675-e693. doi: 10.1210/clinem/dgae251.
4
Skeletal growth is enhanced by a shared role for SOX8 and SOX9 in promoting reserve chondrocyte commitment to columnar proliferation.SOX8 和 SOX9 在促进储备软骨细胞向柱状增殖的定向分化中发挥共同作用,从而增强骨骼生长。
Proc Natl Acad Sci U S A. 2024 Feb 20;121(8):e2316969121. doi: 10.1073/pnas.2316969121. Epub 2024 Feb 12.
5
Transposable elements acquire time- and sex-specific transcriptional and epigenetic signatures along mouse fetal gonad development.转座元件在小鼠胎儿性腺发育过程中获得时间和性别特异性的转录和表观遗传特征。
Front Cell Dev Biol. 2024 Jan 12;11:1327410. doi: 10.3389/fcell.2023.1327410. eCollection 2023.
6
Biallelic Variants Associated With Novel Syndrome With Myopathy, Skeletal Deformities, Intellectual Disability, and Ovarian Dysfunction.与伴有肌病、骨骼畸形、智力障碍和卵巢功能障碍的新型综合征相关的双等位基因变异
Neurol Genet. 2023 Sep 19;9(5):e200088. doi: 10.1212/NXG.0000000000200088. eCollection 2023 Oct.
7
Improving diagnostic precision in primary ovarian insufficiency using comprehensive genetic and autoantibody testing.采用综合基因和自身抗体检测提高原发性卵巢功能不全的诊断精度。
Hum Reprod. 2024 Jan 5;39(1):177-189. doi: 10.1093/humrep/dead233.
8
The study of a hermaphroditic sheep caused by a mutation in the promoter of gene.一项关于由基因启动子突变引起的雌雄同体绵羊的研究。
Vet Anim Sci. 2023 Jul 24;21:100308. doi: 10.1016/j.vas.2023.100308. eCollection 2023 Sep.
9
Genome-Wide Identification, Evolutionary and Mutational Analysis of the Buffalo Sox Gene Family.水牛Sox基因家族的全基因组鉴定、进化与突变分析
Animals (Basel). 2023 Jul 8;13(14):2246. doi: 10.3390/ani13142246.
10
Genetic reanalysis of patients with a difference of sex development carrying the NR5A1/SF-1 variant p.Gly146Ala has discovered other likely disease-causing variations.对携带 NR5A1/SF-1 变异 p.Gly146Ala 的性别发育差异患者进行的基因重新分析发现了其他可能的致病变异。
PLoS One. 2023 Jul 11;18(7):e0287515. doi: 10.1371/journal.pone.0287515. eCollection 2023.
类固醇生成因子1(NR5A1)中反复出现的p.Arg92Trp变异可作为人类性发育中的分子开关。
Hum Mol Genet. 2016 Aug 15;25(16):3446-3453. doi: 10.1093/hmg/ddw186. Epub 2016 Jul 4.
4
Global Disorders of Sex Development Update since 2006: Perceptions, Approach and Care.2006年以来性发育全球疾病最新进展:认识、处理与照护
Horm Res Paediatr. 2016;85(3):158-80. doi: 10.1159/000442975. Epub 2016 Jan 28.
5
Male Reproductive Disorders and Fertility Trends: Influences of Environment and Genetic Susceptibility.男性生殖系统疾病与生育趋势:环境及遗传易感性的影响
Physiol Rev. 2016 Jan;96(1):55-97. doi: 10.1152/physrev.00017.2015.
6
DAX-1 (NR0B1) and steroidogenic factor-1 (SF-1, NR5A1) in human disease.人类疾病中的DAX-1(NR0B1)和类固醇生成因子-1(SF-1,NR5A1)
Best Pract Res Clin Endocrinol Metab. 2015 Aug;29(4):607-19. doi: 10.1016/j.beem.2015.07.004. Epub 2015 Jul 14.
7
Gonadal Identity in the Absence of Pro-Testis Factor SOX9 and Pro-Ovary Factor Beta-Catenin in Mice.小鼠中缺乏睾丸形成因子SOX9和卵巢形成因子β-连环蛋白时的性腺身份
Biol Reprod. 2015 Aug;93(2):35. doi: 10.1095/biolreprod.115.131276. Epub 2015 Jun 24.
8
Thalassemia Intermedia Caused by 16p13.3 Sectional Duplication in a β-Thalassemia Heterozygous Child.一名β地中海贫血杂合子儿童因16p13.3节段重复导致中间型地中海贫血
Pediatr Hematol Oncol. 2015;32(5):349-53. doi: 10.3109/08880018.2015.1040932. Epub 2015 Jun 18.
9
SOXE transcription factors form selective dimers on non-compact DNA motifs through multifaceted interactions between dimerization and high-mobility group domains.SOXE转录因子通过二聚化结构域与高迁移率族结构域之间的多方面相互作用,在非紧密DNA基序上形成选择性二聚体。
Sci Rep. 2015 May 27;5:10398. doi: 10.1038/srep10398.
10
X-linked TEX11 mutations, meiotic arrest, and azoospermia in infertile men.X连锁TEX11突变、减数分裂阻滞与不育男性的无精子症
N Engl J Med. 2015 May 28;372(22):2097-107. doi: 10.1056/NEJMoa1406192. Epub 2015 May 13.