• 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

细胞周期的发育控制:来自.的见解。

Developmental Control of the Cell Cycle: Insights from .

机构信息

Department of Cellular Biology, University of Georgia, Athens, Georgia 30602-2607

Department of Biology, Science 4 Life Program, Faculty of Science, University of Utrecht, 3584CH, The Netherlands

出版信息

Genetics. 2019 Mar;211(3):797-829. doi: 10.1534/genetics.118.301643.

DOI:10.1534/genetics.118.301643
PMID:30846544
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6404260/
Abstract

During animal development, a single fertilized egg forms a complete organism with tens to trillions of cells that encompass a large variety of cell types. Cell cycle regulation is therefore at the center of development and needs to be carried out in close coordination with cell differentiation, migration, and death, as well as tissue formation, morphogenesis, and homeostasis. The timing and frequency of cell divisions are controlled by complex combinations of external and cell-intrinsic signals that vary throughout development. Insight into how such controls determine cell division patterns has come from studies in various genetic model systems. The nematode has only about 1000 somatic cells and approximately twice as many germ cells in the adult hermaphrodite. Despite the relatively small number of cells, has diverse tissues, including intestine, nerves, striated and smooth muscle, and skin. is unique as a model organism for studies of the cell cycle because the somatic cell lineage is invariant. Somatic cells divide at set times during development to produce daughter cells that adopt reproducible developmental fates. Studies in have allowed the identification of conserved cell cycle regulators and provided insights into how cell cycle regulation varies between tissues. In this review, we focus on the regulation of the cell cycle in the context of development, with reference to other systems, with the goal of better understanding how cell cycle regulation is linked to animal development in general.

摘要

在动物发育过程中,一个受精卵形成一个完整的生物体,其中包含数以万计到数万亿的细胞,这些细胞包含多种不同的细胞类型。因此,细胞周期的调控处于发育的中心地位,需要与细胞分化、迁移和死亡以及组织形成、形态发生和体内平衡密切协调。细胞分裂的时间和频率由贯穿整个发育过程的外部和细胞内在信号的复杂组合来控制。对这些控制如何决定细胞分裂模式的深入了解来自于各种遗传模式生物的研究。线虫只有大约 1000 个体细胞和约两倍的生殖细胞在成年雌雄同体中。尽管细胞数量相对较少,但线虫具有多种组织,包括肠道、神经、横纹肌和平滑肌以及皮肤。线虫是研究细胞周期的独特模式生物,因为体细胞谱系是不变的。体细胞在发育过程中的特定时间分裂,产生具有可重复发育命运的子细胞。对线虫的研究鉴定了保守的细胞周期调控因子,并深入了解了细胞周期调控在不同组织之间的差异。在这篇综述中,我们将重点讨论细胞周期在 发育过程中的调控,并参考其他系统,以期更好地理解细胞周期调控与动物发育的总体联系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/435e/6404260/e92d314b308d/797f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/435e/6404260/6114f4381b7a/797f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/435e/6404260/df82a51cb2cd/797f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/435e/6404260/e918ad0b0749/797f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/435e/6404260/b1a07b55f1f0/797f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/435e/6404260/80a80e7505ad/797f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/435e/6404260/ade3d0f3b9cf/797f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/435e/6404260/cab405184254/797f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/435e/6404260/e92d314b308d/797f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/435e/6404260/6114f4381b7a/797f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/435e/6404260/df82a51cb2cd/797f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/435e/6404260/e918ad0b0749/797f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/435e/6404260/b1a07b55f1f0/797f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/435e/6404260/80a80e7505ad/797f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/435e/6404260/ade3d0f3b9cf/797f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/435e/6404260/cab405184254/797f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/435e/6404260/e92d314b308d/797f8.jpg

相似文献

1
Developmental Control of the Cell Cycle: Insights from .细胞周期的发育控制:来自.的见解。
Genetics. 2019 Mar;211(3):797-829. doi: 10.1534/genetics.118.301643.
2
The cell cycle and development: lessons from C. elegans.细胞周期与发育:秀丽隐杆线虫的启示
Semin Cell Dev Biol. 2005 Jun;16(3):397-406. doi: 10.1016/j.semcdb.2005.02.002.
3
Control of developmental timing by micrornas and their targets.微小RNA及其靶标对发育时间的调控。
Annu Rev Cell Dev Biol. 2002;18:495-513. doi: 10.1146/annurev.cellbio.18.012502.105832. Epub 2002 Apr 2.
4
The temporal control of cell cycle and cell fate in Caenorhabditis elegans.秀丽隐杆线虫细胞周期和细胞命运的时序控制。
Novartis Found Symp. 2001;237:203-14; discussion 214-20. doi: 10.1002/0470846666.ch16.
5
A germ cell determinant reveals parallel pathways for germ line development in Caenorhabditis elegans.一种生殖细胞决定因素揭示了秀丽隐杆线虫生殖系发育的平行途径。
Development. 2015 Oct 15;142(20):3571-82. doi: 10.1242/dev.125732. Epub 2015 Sep 22.
6
Vulval development in Caenorhabditis elegans.秀丽隐杆线虫的外阴发育
Trends Genet. 1997 Feb;13(2):55-61. doi: 10.1016/s0168-9525(97)01005-6.
7
Combinatorial decoding of the invariant C. elegans embryonic lineage in space and time.秀丽隐杆线虫胚胎不变细胞谱系在空间和时间上的组合解码
Genesis. 2016 Apr;54(4):182-97. doi: 10.1002/dvg.22928. Epub 2016 Mar 19.
8
Essential embryonic roles of the CKI-1 cyclin-dependent kinase inhibitor in cell-cycle exit and morphogenesis in C elegans.CKI-1细胞周期蛋白依赖性激酶抑制剂在秀丽隐杆线虫细胞周期退出和形态发生中的重要胚胎作用。
Dev Biol. 2003 Aug 1;260(1):273-86. doi: 10.1016/s0012-1606(03)00239-2.
9
C. elegans cell cycle analysis.秀丽隐杆线虫细胞周期分析。
Methods Cell Biol. 2012;107:265-94. doi: 10.1016/B978-0-12-394620-1.00009-6.
10
Visualizing the metazoan proliferation-quiescence decision in vivo.在体可视化后生动物增殖-静止决策。
Elife. 2020 Dec 22;9:e63265. doi: 10.7554/eLife.63265.

引用本文的文献

1
Chromosomes remain individualized through interphase in embryos of the tardigrade .在缓步动物胚胎的间期,染色体保持独立状态。
bioRxiv. 2025 Jul 28:2025.07.25.666853. doi: 10.1101/2025.07.25.666853.
2
Folate-based binuclear Mn(II) chelates with 2,2'-bipyridine/1,10-phenanthroline as targeted anticancer agents for colon cancer cells.以叶酸为基础、2,2'-联吡啶/1,10-菲啰啉为配体的双核锰(II)螯合物作为针对结肠癌细胞的靶向抗癌剂。
Sci Rep. 2025 Jul 31;15(1):27905. doi: 10.1038/s41598-025-12251-9.
3
Notch controls APC/C to enable accumulation of chromatin regulators in germline stem cells from .

本文引用的文献

1
Initiation of Meiotic Development Is Controlled by Three Post-transcriptional Pathways in .在 中,减数分裂的起始由三个转录后途径控制。
Genetics. 2018 Aug;209(4):1197-1224. doi: 10.1534/genetics.118.300985. Epub 2018 Jun 25.
2
Loss of the Caenorhabditis elegans pocket protein LIN-35 reveals MuvB's innate function as the repressor of DREAM target genes.秀丽隐杆线虫口袋蛋白LIN-35的缺失揭示了MuvB作为DREAM靶基因阻遏物的固有功能。
PLoS Genet. 2017 Nov 1;13(11):e1007088. doi: 10.1371/journal.pgen.1007088. eCollection 2017 Nov.
3
Dafachronic acid inhibits C. elegans germ cell proliferation in a DAF-12-dependent manner.
Notch控制后期促进复合体/细胞周期体(APC/C),以使生殖系干细胞中染色质调节因子得以积累。
Sci Adv. 2025 May 30;11(22):eadu8572. doi: 10.1126/sciadv.adu8572.
4
Mitochondrial fission surveillance is coupled to Caenorhabditis elegans DNA and chromosome segregation integrity.线粒体裂变监测与秀丽隐杆线虫的DNA及染色体分离完整性相关联。
PLoS Genet. 2025 Apr 25;21(4):e1011678. doi: 10.1371/journal.pgen.1011678. eCollection 2025 Apr.
5
Differential effect of ubiquitous and germline depletion of Integrator complex function on C. elegans physiology.整合子复合体功能的普遍缺失和种系缺失对秀丽隐杆线虫生理学的差异影响。
Biol Open. 2025 Apr 15;14(4). doi: 10.1242/bio.061930. Epub 2025 Apr 10.
6
EFL-3/E2F7 modulates Wnt signalling by repressing the Nemo-like kinase LIT-1 during asymmetric epidermal cell division in Caenorhabditis elegans.在秀丽隐杆线虫不对称表皮细胞分裂过程中,EFL-3/E2F7通过抑制类Nemo激酶LIT-1来调节Wnt信号通路。
Development. 2025 Mar 1;152(5). doi: 10.1242/dev.204546. Epub 2025 Mar 3.
7
Impact of G1 phase kinetics on the acquisition of stemness in cancer cells: the critical role of cyclin D.G1期动力学对癌细胞干性获得的影响:细胞周期蛋白D的关键作用。
Mol Biol Rep. 2025 Feb 14;52(1):230. doi: 10.1007/s11033-025-10351-3.
8
SEM-2/SoxC regulates multiple aspects of C. elegans postembryonic mesoderm development.SEM-2/SoxC调控秀丽隐杆线虫胚后中胚层发育的多个方面。
PLoS Genet. 2025 Jan 21;21(1):e1011361. doi: 10.1371/journal.pgen.1011361. eCollection 2025 Jan.
9
Quantitative perturbation-phenotype maps reveal nonlinear responses underlying robustness of PAR-dependent asymmetric cell division.定量扰动-表型图谱揭示了PAR依赖的不对称细胞分裂稳健性背后的非线性反应。
PLoS Biol. 2024 Dec 9;22(12):e3002437. doi: 10.1371/journal.pbio.3002437. eCollection 2024 Dec.
10
Evolution of the Cdk4/6-Cdkn2 system in invertebrates.无脊椎动物中 CDK4/6-Cdkn2 系统的进化。
Genes Cells. 2024 Nov;29(11):1037-1051. doi: 10.1111/gtc.13165. Epub 2024 Oct 8.
法尼醇X受体激动剂以DAF-12依赖的方式抑制秀丽隐杆线虫生殖细胞增殖。
Dev Biol. 2017 Dec 15;432(2):215-221. doi: 10.1016/j.ydbio.2017.10.014. Epub 2017 Oct 21.
4
LIN-41 and OMA Ribonucleoprotein Complexes Mediate a Translational Repression-to-Activation Switch Controlling Oocyte Meiotic Maturation and the Oocyte-to-Embryo Transition in .LIN-41和OMA核糖核蛋白复合物介导翻译抑制到激活的转换,控制卵母细胞减数分裂成熟以及卵母细胞到胚胎的转变。
Genetics. 2017 Aug;206(4):2007-2039. doi: 10.1534/genetics.117.203174. Epub 2017 Jun 1.
5
Asymmetric Cell Division in the One-Cell C. elegans Embryo: Multiple Steps to Generate Cell Size Asymmetry.秀丽隐杆线虫单细胞胚胎中的不对称细胞分裂:产生细胞大小不对称的多个步骤。
Results Probl Cell Differ. 2017;61:115-140. doi: 10.1007/978-3-319-53150-2_5.
6
Live-imaging analysis of germ cell proliferation in the C. elegans adult supports a stochastic model for stem cell proliferation.秀丽隐杆线虫成虫生殖细胞增殖的实时成像分析支持干细胞增殖的随机模型。
Dev Biol. 2017 Mar 15;423(2):93-100. doi: 10.1016/j.ydbio.2017.02.008. Epub 2017 Feb 17.
7
Regulation of DNA Replication in Early Embryonic Cleavages.早期胚胎卵裂中DNA复制的调控
Genes (Basel). 2017 Jan 19;8(1):42. doi: 10.3390/genes8010042.
8
Regulation and Function of Cdt1; A Key Factor in Cell Proliferation and Genome Stability.Cdt1的调控与功能:细胞增殖和基因组稳定性的关键因素
Genes (Basel). 2016 Dec 22;8(1):2. doi: 10.3390/genes8010002.
9
Replication fork instability and the consequences of fork collisions from rereplication.复制叉不稳定性及再复制导致的复制叉碰撞后果。
Genes Dev. 2016 Oct 15;30(20):2241-2252. doi: 10.1101/gad.288142.116.
10
LIN-23, an E3 Ubiquitin Ligase Component, Is Required for the Repression of CDC-25.2 Activity during Intestinal Development in .LIN-23,一种E3泛素连接酶成分,在肠道发育过程中抑制CDC-25.2活性是必需的。
Mol Cells. 2016 Nov 30;39(11):834-840. doi: 10.14348/molcells.2016.0238. Epub 2016 Nov 18.