• 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

SWI/SNF 染色质重塑亚基 Smarca4/BRG1 对雌性生育力至关重要†。

SWI/SNF chromatin remodeling subunit Smarca4/BRG1 is essential for female fertility†.

机构信息

Department of Cellular and Molecular Medicine, University of Ottawa, Ottawa, ON, Canada.

Cancer Therapeutics Program, Ottawa Hospital Research Institute, Ottawa, ON, Canada.

出版信息

Biol Reprod. 2023 Feb 13;108(2):279-291. doi: 10.1093/biolre/ioac209.

DOI:10.1093/biolre/ioac209
PMID:36440965
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9930400/
Abstract

Mammalian folliculogenesis is a complex process that involves the regulation of chromatin structure for gene expression and oocyte meiotic resumption. The SWI/SNF complex is a chromatin remodeler using either Brahma-regulated gene 1 (BRG1) or BRM (encoded by Smarca4 and Smarca2, respectively) as its catalytic subunit. SMARCA4 loss of expression is associated with a rare type of ovarian cancer; however, its function during folliculogenesis remains poorly understood. In this study, we describe the phenotype of BRG1 mutant mice to better understand its role in female fertility. Although no tumor emerged from BRG1 mutant mice, conditional depletion of Brg1 in the granulosa cells (GCs) of Brg1fl/fl;Amhr2-Cre mice caused sterility, whereas conditional depletion of Brg1 in the oocytes of Brg1fl/fl;Gdf9-Cre mice resulted in subfertility. Recovery of cumulus-oocyte complexes after natural mating or superovulation showed no significant difference in the Brg1fl/fl;Amhr2-Cre mutant mice and significantly fewer oocytes in the Brg1fl/fl;Gdf9-Cre mutant mice compared with controls, which may account for the subfertility. Interestingly, the evaluation of oocyte developmental competence by in vitro culture of retrieved two-cell embryos indicated that oocytes originating from the Brg1fl/fl;Amhr2-Cre mice did not reach the blastocyst stage and had higher rates of mitotic defects, including micronuclei. Together, these results indicate that BRG1 plays an important role in female fertility by regulating granulosa and oocyte functions during follicle growth and is needed for the acquisition of oocyte developmental competence.

摘要

哺乳动物卵泡发生是一个复杂的过程,涉及染色质结构的调控以实现基因表达和卵母细胞减数分裂恢复。SWI/SNF 复合物是一种染色质重塑酶,使用 Brahma 调节基因 1 (BRG1) 或 BRM(分别由 Smarca4 和 Smarca2 编码)作为其催化亚基。SMARCA4 表达缺失与一种罕见的卵巢癌有关;然而,其在卵泡发生中的功能仍知之甚少。在这项研究中,我们描述了 BRG1 突变小鼠的表型,以更好地了解其在雌性生育力中的作用。尽管 BRG1 突变小鼠没有出现肿瘤,但 Brg1fl/fl;Amhr2-Cre 小鼠的颗粒细胞 (GC) 中 Brg1 的条件性缺失导致不育,而 Brg1fl/fl;Gdf9-Cre 小鼠的卵母细胞中 Brg1 的条件性缺失导致生育力下降。自然交配或超排卵后回收的卵丘-卵母细胞复合物显示,Brg1fl/fl;Amhr2-Cre 突变小鼠中没有明显差异,而 Brg1fl/fl;Gdf9-Cre 突变小鼠中的卵母细胞明显减少,这可能是生育力下降的原因。有趣的是,通过体外培养回收的二细胞胚胎评估卵母细胞发育能力表明,来自 Brg1fl/fl;Amhr2-Cre 小鼠的卵母细胞未能达到囊胚阶段,并且具有更高的有丝分裂缺陷率,包括微核。总之,这些结果表明,BRG1 通过调节卵泡生长过程中的颗粒细胞和卵母细胞功能在雌性生育力中发挥重要作用,并且需要获得卵母细胞发育能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a906/9930400/a21c6432b2a8/ioac209f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a906/9930400/ded958a78ef9/ioac209ga.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a906/9930400/9d45070fdb31/ioac209f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a906/9930400/35e17e32bf57/ioac209f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a906/9930400/4a1f965abf10/ioac209f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a906/9930400/2ec6e854bdb3/ioac209f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a906/9930400/481d8ad03f20/ioac209f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a906/9930400/087efc012959/ioac209f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a906/9930400/a21c6432b2a8/ioac209f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a906/9930400/ded958a78ef9/ioac209ga.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a906/9930400/9d45070fdb31/ioac209f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a906/9930400/35e17e32bf57/ioac209f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a906/9930400/4a1f965abf10/ioac209f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a906/9930400/2ec6e854bdb3/ioac209f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a906/9930400/481d8ad03f20/ioac209f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a906/9930400/087efc012959/ioac209f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a906/9930400/a21c6432b2a8/ioac209f7.jpg

相似文献

1
SWI/SNF chromatin remodeling subunit Smarca4/BRG1 is essential for female fertility†.SWI/SNF 染色质重塑亚基 Smarca4/BRG1 对雌性生育力至关重要†。
Biol Reprod. 2023 Feb 13;108(2):279-291. doi: 10.1093/biolre/ioac209.
2
The chromatin-remodeling enzyme BRG1 plays an essential role in primitive erythropoiesis and vascular development.染色质重塑酶BRG1在原始红细胞生成和血管发育中起着至关重要的作用。
Development. 2008 Feb;135(3):493-500. doi: 10.1242/dev.010090. Epub 2007 Dec 19.
3
Loss of the SWI/SNF-ATPase subunit members SMARCF1 (ARID1A), SMARCA2 (BRM), SMARCA4 (BRG1) and SMARCB1 (INI1) in oesophageal adenocarcinoma.食管腺癌中 SWI/SNF-ATP 酶亚基成员 SMARCF1(ARID1A)、SMARCA2(BRM)、SMARCA4(BRG1)和 SMARCB1(INI1)的缺失。
BMC Cancer. 2020 Jan 6;20(1):12. doi: 10.1186/s12885-019-6425-3.
4
Residual complexes containing SMARCA2 (BRM) underlie the oncogenic drive of SMARCA4 (BRG1) mutation.残余复合物包含 SMARCA2(BRM),是 SMARCA4(BRG1)突变致癌驱动的基础。
Mol Cell Biol. 2014 Mar;34(6):1136-44. doi: 10.1128/MCB.01372-13. Epub 2014 Jan 13.
5
SWI/SNF chromatin-remodeling enzymes Brahma-related gene 1 (BRG1) and Brahma (BRM) are dispensable in multiple models of postnatal angiogenesis but are required for vascular integrity in infant mice.SWI/SNF染色质重塑酶相关基因1(BRG1)和BRM在出生后血管生成的多种模型中并非必需,但对幼鼠的血管完整性却是必需的。
J Am Heart Assoc. 2015 Apr 22;4(4):e001972. doi: 10.1161/JAHA.115.001972.
6
The BRG1 chromatin remodeler protects against ovarian cysts, uterine tumors, and mammary tumors in a lineage-specific manner.BRG1 染色质重塑因子以谱系特异性方式保护卵巢囊肿、子宫肿瘤和乳腺肿瘤。
PLoS One. 2012;7(2):e31346. doi: 10.1371/journal.pone.0031346. Epub 2012 Feb 21.
7
Dual loss of the SWI/SNF complex ATPases SMARCA4/BRG1 and SMARCA2/BRM is highly sensitive and specific for small cell carcinoma of the ovary, hypercalcaemic type.SWI/SNF复合物ATP酶SMARCA4/BRG1和SMARCA2/BRM的双重缺失对高钙血症型卵巢小细胞癌具有高度敏感性和特异性。
J Pathol. 2016 Feb;238(3):389-400. doi: 10.1002/path.4633. Epub 2015 Dec 21.
8
Discovery of Orally Active Inhibitors of Brahma Homolog (BRM)/SMARCA2 ATPase Activity for the Treatment of Brahma Related Gene 1 (BRG1)/SMARCA4-Mutant Cancers.发现具有口服活性的 Brama 同源物(BRM)/SMARCA2 ATP 酶活性抑制剂,用于治疗 Brama 相关基因 1(BRG1)/SMARCA4 突变型癌症。
J Med Chem. 2018 Nov 21;61(22):10155-10172. doi: 10.1021/acs.jmedchem.8b01318. Epub 2018 Oct 31.
9
Maternal BRG1 regulates zygotic genome activation in the mouse.母体BRG1调控小鼠合子基因组激活。
Genes Dev. 2006 Jul 1;20(13):1744-54. doi: 10.1101/gad.1435106.
10
SWI/SNF chromatin remodeler complex within the reward pathway is required for behavioral adaptations to stress.SWI/SNF 染色质重塑复合物存在于奖励通路中,对于应激相关的行为适应是必需的。
Nat Commun. 2022 Apr 4;13(1):1807. doi: 10.1038/s41467-022-29380-8.

引用本文的文献

1
Aberrant SWI/SNF Complex Members Are Predominant in Rare Ovarian Malignancies-Therapeutic Vulnerabilities in Treatment-Resistant Subtypes.异常的SWI/SNF复合物成员在罕见卵巢恶性肿瘤中占主导地位——耐药亚型中的治疗脆弱性。
Cancers (Basel). 2024 Sep 3;16(17):3068. doi: 10.3390/cancers16173068.
2
The chromatin accessibility landscape of mouse oocytes during configuration transition.小鼠卵母细胞在构型转变过程中的染色质可及性图谱。
Cell Prolif. 2025 Jan;58(1):e13733. doi: 10.1111/cpr.13733. Epub 2024 Sep 8.

本文引用的文献

1
BRG1 Activates Proliferation and Transcription of Cell Cycle-Dependent Genes in Breast Cancer Cells.BRG1激活乳腺癌细胞中细胞周期依赖性基因的增殖和转录。
Cancers (Basel). 2020 Feb 4;12(2):349. doi: 10.3390/cancers12020349.
2
Orbit Image Analysis: An open-source whole slide image analysis tool.眼眶图像分析:一个开源的全玻片图像分析工具。
PLoS Comput Biol. 2020 Feb 5;16(2):e1007313. doi: 10.1371/journal.pcbi.1007313. eCollection 2020 Feb.
3
Brg1 promotes liver regeneration after partial hepatectomy via regulation of cell cycle.
Brg1 通过调控细胞周期促进肝部分切除术后的肝再生。
Sci Rep. 2019 Feb 20;9(1):2320. doi: 10.1038/s41598-019-38568-w.
4
Transcriptome Landscape of Human Folliculogenesis Reveals Oocyte and Granulosa Cell Interactions.人类卵泡发生的转录组全景揭示了卵母细胞和颗粒细胞的相互作用。
Mol Cell. 2018 Dec 20;72(6):1021-1034.e4. doi: 10.1016/j.molcel.2018.10.029. Epub 2018 Nov 21.
5
Regulation of ATM and ATR by SMARCAL1 and BRG1.SMARCAL1 和 BRG1 对 ATM 和 ATR 的调节。
Biochim Biophys Acta Gene Regul Mech. 2018 Dec;1861(12):1076-1092. doi: 10.1016/j.bbagrm.2018.10.004. Epub 2018 Oct 11.
6
The maternal-to-zygotic transition in bovine in vitro-fertilized embryos is associated with marked changes in small non-coding RNAs†.牛体外受精胚胎的母源到合子的转变与小非编码 RNA 的显著变化有关†。
Biol Reprod. 2019 Feb 1;100(2):331-350. doi: 10.1093/biolre/ioy190.
7
Follicle capacitation: a meta-analysis to investigate the transcriptome dynamics following follicle-stimulating hormone decline in bovine granulosa cells.卵母细胞成熟:一项关于牛颗粒细胞中卵泡刺激素下降后转录组动态的荟萃分析。
Biol Reprod. 2018 Oct 1;99(4):877-887. doi: 10.1093/biolre/ioy090.
8
The SWI/SNF complex subunit genes: Their functions, variations, and links to risk and survival outcomes in human cancers.SWI/SNF 复合物亚基基因:它们在人类癌症中的功能、变异及与风险和生存结局的关系。
Crit Rev Oncol Hematol. 2018 Mar;123:114-131. doi: 10.1016/j.critrevonc.2018.01.009. Epub 2018 Feb 6.
9
Acquisition of oocyte competence to develop as an embryo: integrated nuclear and cytoplasmic events.卵母细胞获得胚胎发育能力的过程:核质综合事件。
Hum Reprod Update. 2018 May 1;24(3):245-266. doi: 10.1093/humupd/dmx040.
10
Molecular evidence that follicle development is accelerated compared to .与……相比,卵泡发育加速的分子证据。 (原句不完整,翻译可能存在一定局限性)
Reproduction. 2017 May;153(5):493-508. doi: 10.1530/REP-16-0627. Epub 2017 Feb 2.