• 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

两个 microRNAs 足以用于线虫的胚胎模式形成。

Two MicroRNAs Are Sufficient for Embryonic Patterning in C. elegans.

机构信息

Research Institute of Molecular Pathology (IMP), Vienna BioCenter (VBC), Campus-Vienna-Biocenter 1, 1030 Vienna, Austria.

Research Institute of Molecular Pathology (IMP), Vienna BioCenter (VBC), Campus-Vienna-Biocenter 1, 1030 Vienna, Austria.

出版信息

Curr Biol. 2020 Dec 21;30(24):5058-5065.e5. doi: 10.1016/j.cub.2020.09.066. Epub 2020 Oct 29.

DOI:10.1016/j.cub.2020.09.066
PMID:33125867
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7758728/
Abstract

MicroRNAs (miRNAs) are a class of post-transcriptional repressors with diverse roles in animal development and physiology [1]. The Microprocessor complex, composed of Drosha and Pasha/DGCR8, is necessary for the biogenesis of all canonical miRNAs and essential for the early stages of animal embryogenesis [2-8]. However, the cause for this requirement is largely unknown. Animals often express hundreds of miRNAs, and it remains unclear whether the Microprocessor is required to produce one or few essential miRNAs or many individually non-essential miRNAs. Additionally, both Drosha and Pasha/DGCR8 bind and cleave a variety of non-miRNA substrates [9-15], and it is unknown whether these activities account for the Microprocessor's essential requirement. To distinguish between these possibilities, we developed a system in C. elegans to stringently deplete embryos of Microprocessor activity. Using a combination of auxin-inducible degradation (AID) and RNA interference (RNAi), we achieved Drosha and Pasha/DGCR8 depletion starting in the maternal germline, resulting in Microprocessor and miRNA-depleted embryos, which fail to undergo morphogenesis or form organs. Using a Microprocessor-bypass strategy, we show that this early embryonic arrest is rescued by the addition of just two miRNAs, one miR-35 and one miR-51 family member, resulting in morphologically normal larvae. Thus, just two out of ∼150 canonical miRNAs are sufficient for morphogenesis and organogenesis, and the processing of these miRNAs accounts for the essential requirement for Drosha and Pasha/DGCR8 during the early stages of C. elegans embryonic development. VIDEO ABSTRACT.

摘要

微小 RNA(miRNA)是一类在后转录水平起调控作用的分子,在动物发育和生理过程中具有广泛的功能[1]。Microprocessor 复合物由 Drosha 和 Pasha/DGCR8 组成,是所有经典 miRNA 生物发生所必需的,对于动物胚胎早期发育也至关重要[2-8]。然而,造成这种必需性的原因在很大程度上尚不清楚。动物通常表达数百种 miRNA,目前仍不清楚 Microprocessor 是否需要产生一种或少数几种必需的 miRNA,还是产生许多单独非必需的 miRNA。此外,Drosha 和 Pasha/DGCR8 都能结合和切割多种非 miRNA 底物[9-15],而这些活性是否解释了 Microprocessor 的必需性要求尚不清楚。为了区分这些可能性,我们在秀丽隐杆线虫中开发了一种严格耗尽 Microprocessor 活性的系统。我们结合使用生长素诱导降解(AID)和 RNA 干扰(RNAi),从母系生殖系开始实现 Drosha 和 Pasha/DGCR8 的耗尽,导致 Microprocessor 和 miRNA 耗尽的胚胎无法进行形态发生或形成器官。通过使用 Microprocessor 旁路策略,我们表明,通过添加仅两种 miRNA(miR-35 和一种 miR-51 家族成员)即可挽救这种早期胚胎阻滞,从而产生形态正常的幼虫。因此,仅两种约 150 种经典 miRNA 就足以进行形态发生和器官发生,并且这些 miRNA 的加工解释了 Drosha 和 Pasha/DGCR8 在秀丽隐杆线虫胚胎发育早期的必需性要求。视频摘要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75f4/7758728/2b08b4925bae/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75f4/7758728/0856e1f41379/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75f4/7758728/dc66d65c1c3e/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75f4/7758728/36f6045bc7bd/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75f4/7758728/e3bdbed826e2/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75f4/7758728/2b08b4925bae/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75f4/7758728/0856e1f41379/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75f4/7758728/dc66d65c1c3e/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75f4/7758728/36f6045bc7bd/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75f4/7758728/e3bdbed826e2/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75f4/7758728/2b08b4925bae/gr4.jpg

相似文献

1
Two MicroRNAs Are Sufficient for Embryonic Patterning in C. elegans.两个 microRNAs 足以用于线虫的胚胎模式形成。
Curr Biol. 2020 Dec 21;30(24):5058-5065.e5. doi: 10.1016/j.cub.2020.09.066. Epub 2020 Oct 29.
2
Dissection of the Caenorhabditis elegans Microprocessor.秀丽隐杆线虫微处理器的剖析。
Nucleic Acids Res. 2023 Feb 28;51(4):1512-1527. doi: 10.1093/nar/gkac1170.
3
Processing of primary microRNAs by the Microprocessor complex.微处理器复合体对初级微小RNA的加工
Nature. 2004 Nov 11;432(7014):231-5. doi: 10.1038/nature03049. Epub 2004 Nov 7.
4
Genome-wide identification of targets of the drosha-pasha/DGCR8 complex.全基因组范围内对Drosha-pasha/DGCR8复合物靶点的鉴定。
RNA. 2009 Apr;15(4):537-45. doi: 10.1261/rna.1319309. Epub 2009 Feb 17.
5
Functional analysis of microRNA pathway genes in the somatic gonad and germ cells during ovulation in C. elegans.秀丽隐杆线虫排卵过程中体细胞性腺和生殖细胞中微小RNA通路基因的功能分析。
Dev Biol. 2017 Jun 1;426(1):115-125. doi: 10.1016/j.ydbio.2017.04.007. Epub 2017 Apr 28.
6
MicroRNA-dependent roles of Drosha and Pasha in the Drosophila larval ovary morphogenesis.Drosha和Pasha在果蝇幼虫卵巢形态发生中的微小RNA依赖性作用。
Dev Biol. 2016 Aug 15;416(2):312-23. doi: 10.1016/j.ydbio.2016.06.026. Epub 2016 Jun 20.
7
Noncanonical processing by animal Microprocessor.动物 Microprocessor 的非规范加工。
Mol Cell. 2023 Jun 1;83(11):1810-1826.e8. doi: 10.1016/j.molcel.2023.05.004.
8
Drosha-independent DGCR8/Pasha pathway regulates neuronal morphogenesis.Drosha 非依赖性 DGCR8/Pasha 通路调控神经元形态发生。
Proc Natl Acad Sci U S A. 2014 Jan 28;111(4):1421-6. doi: 10.1073/pnas.1318445111. Epub 2014 Jan 13.
9
Characterization of DGCR8/Pasha, the essential cofactor for Drosha in primary miRNA processing.DGCR8/Pasha的特性,其为初级miRNA加工过程中Drosha的必需辅因子。
Nucleic Acids Res. 2006;34(16):4622-9. doi: 10.1093/nar/gkl458. Epub 2006 Sep 8.
10
Post-transcriptional control of DGCR8 expression by the Microprocessor.微处理器对DGCR8表达的转录后调控。
RNA. 2009 Jun;15(6):1005-11. doi: 10.1261/rna.1591709. Epub 2009 Apr 21.

引用本文的文献

1
An ancient and essential miRNA family controls cellular interaction pathways in .一个古老且重要的微小RNA家族控制着……中的细胞相互作用途径。
Sci Adv. 2025 Sep 5;11(36):eadz1934. doi: 10.1126/sciadv.adz1934. Epub 2025 Sep 3.
2
A lncRNA drives developmentally-timed decay of all members of an essential microRNA family.一种长链非编码RNA驱动一个重要微小RNA家族所有成员的发育定时降解。
bioRxiv. 2025 Jul 31:2025.07.30.667716. doi: 10.1101/2025.07.30.667716.
3
A noncanonical Pol III-dependent, Microprocessor-independent biogenesis pathway generates a germline enriched miRNA family.
一条非经典的依赖于Pol III且不依赖于微处理器的生物合成途径产生了一个在生殖系中富集的miRNA家族。
bioRxiv. 2025 Jun 2:2025.04.11.648421. doi: 10.1101/2025.04.11.648421.
4
Widespread destabilization of microRNAs by the E3 ubiquitin ligase EBAX-1.E3泛素连接酶EBAX-1导致微小RNA广泛失稳
RNA. 2024 Dec 16;31(1):51-66. doi: 10.1261/rna.080276.124.
5
Mime-seq 2.0: a method to sequence microRNAs from specific mouse cell types.Mime-seq 2.0:一种从特定的小鼠细胞类型中测序 microRNAs 的方法。
EMBO J. 2024 Jun;43(12):2506-2525. doi: 10.1038/s44318-024-00102-8. Epub 2024 Apr 30.
6
A lineage-resolved cartography of microRNA promoter activity in C. elegans empowers multidimensional developmental analysis.线虫中 miRNA 启动子活性的谱系解析图谱为多维发育分析提供了支持。
Nat Commun. 2024 Mar 30;15(1):2783. doi: 10.1038/s41467-024-47055-4.
7
Dynamics of miRNA accumulation during C. elegans larval development.秀丽隐杆线虫幼虫发育过程中 miRNA 积累的动态变化。
Nucleic Acids Res. 2024 May 22;52(9):5336-5355. doi: 10.1093/nar/gkae115.
8
Expression, not sequence, distinguishes miR-238 from its miR-239ab sister miRNAs in promoting longevity in Caenorhabditis elegans.表达而非序列区分了 miR-238 和其 miR-239ab 姐妹 miRNA,使其在秀丽隐杆线虫中促进长寿。
PLoS Genet. 2023 Nov 27;19(11):e1011055. doi: 10.1371/journal.pgen.1011055. eCollection 2023 Nov.
9
Mechanisms of lineage specification in Caenorhabditis elegans.线虫中谱系特化的机制。
Genetics. 2023 Dec 6;225(4). doi: 10.1093/genetics/iyad174.
10
A Compilation of the Diverse miRNA Functions in and Development.miRNA 在 和 发育中的多种功能汇编。
Int J Mol Sci. 2023 Apr 9;24(8):6963. doi: 10.3390/ijms24086963.