Suppr超能文献

秀丽隐杆线虫表皮建立和模式形成所需合子基因座的缺陷筛选。

A deficiency screen for zygotic loci required for establishment and patterning of the epidermis in Caenorhabditis elegans.

作者信息

Terns R M, Kroll-Conner P, Zhu J, Chung S, Rothman J H

机构信息

Department of Biochemistry, University of Wisconsin, Madison 53706, USA.

出版信息

Genetics. 1997 May;146(1):185-206. doi: 10.1093/genetics/146.1.185.

Abstract

To identify genomic regions required for establishment and patterning of the epidermis, we screened 58 deficiencies that collectively delete at least approximately 67% of the Caenorhabditis elegans genome. The epidermal pattern of deficiency homozygous embryos was analyzed by examining expression of a marker specific for one of the three major epidermal cell types, the seam cells. The organization of the epidermis and internal organs was also analyzed using a monoclonal antibody specific for epithelial adherens junctions. While seven deficiencies had no apparent effect on seam cell production, 21 were found to result in subnormal, and five in excess numbers of these cells. An additional 23 deficiencies blocked expression of the seam cell marker, in some cases without preventing cell proliferation. Two deficiencies result in multinucleate seam cells. Deficiencies were also identified that result in subnormal numbers of epidermal cells, hyperfusion of epidermal cells into a large syncytium, or aberrant epidermal differentiation. Finally, analysis of internal epithelia revealed deficiencies that cause defects in formation of internal organs, including circularization of the intestine and bifurcation of the pharynx lumen. This study reveals that many regions of the C. elegans genome are required zygotically for patterning of the epidermis and other epithelia.

摘要

为了确定表皮建立和模式形成所需的基因组区域,我们筛选了58个缺失突变体,这些突变体共同缺失了秀丽隐杆线虫基因组中至少约67%的区域。通过检测一种针对三种主要表皮细胞类型之一——边缘细胞的标记物的表达,来分析缺失纯合胚胎的表皮模式。还使用一种针对上皮黏着连接的单克隆抗体分析了表皮和内部器官的组织结构。虽然有7个缺失突变体对边缘细胞的产生没有明显影响,但发现有21个导致边缘细胞数量低于正常水平,5个导致边缘细胞数量过多。另外23个缺失突变体阻断了边缘细胞标记物的表达,在某些情况下并不妨碍细胞增殖。有两个缺失突变体导致多核边缘细胞。还鉴定出了一些缺失突变体,它们导致表皮细胞数量低于正常水平、表皮细胞过度融合形成一个大的合胞体或表皮分化异常。最后,对内部上皮组织的分析揭示了一些缺失突变体,它们导致内部器官形成缺陷,包括肠道环化和咽腔分叉。这项研究表明,秀丽隐杆线虫基因组的许多区域在合子阶段对于表皮和其他上皮组织的模式形成是必需的。

相似文献

2
Caudal-dependent cell positioning directs morphogenesis of the C. elegans ventral epidermis.
Dev Biol. 2020 May 1;461(1):31-42. doi: 10.1016/j.ydbio.2020.01.001. Epub 2020 Jan 7.
5
The Caenorhabditis elegans nuclear receptor gene nhr-25 regulates epidermal cell development.
Mol Cell Biol. 2004 Sep;24(17):7345-58. doi: 10.1128/MCB.24.17.7345-7358.2004.
7
Gene expression profiling of epidermal cell types in C. elegans using Targeted DamID.
Development. 2021 Sep 1;148(17). doi: 10.1242/dev.199452. Epub 2021 Sep 3.
8
ceh-16/engrailed patterns the embryonic epidermis of Caenorhabditis elegans.
Development. 2005 Feb;132(4):739-49. doi: 10.1242/dev.01638. Epub 2005 Jan 19.
10
Cell contact regulates neuroblast formation in the Caenorhabditis elegans lateral epidermis.
Development. 1994 Feb;120(2):313-23. doi: 10.1242/dev.120.2.313.

引用本文的文献

1
UBR-5 and UBE2D mediate timely exit from stem fate via destabilization of poly(A)-binding protein PABP-2 in cell state transition.
Proc Natl Acad Sci U S A. 2024 Oct 22;121(43):e2407561121. doi: 10.1073/pnas.2407561121. Epub 2024 Oct 15.
4
Heterochronic Phenotype Analysis of Hypodermal Seam Cells in .
Bio Protoc. 2019 Jan 5;9(1). doi: 10.21769/BioProtoc.3132.
6
Stochastic loss and gain of symmetric divisions in the C. elegans epidermis perturbs robustness of stem cell number.
PLoS Biol. 2017 Nov 6;15(11):e2002429. doi: 10.1371/journal.pbio.2002429. eCollection 2017 Nov.
7
A Network of Chromatin Factors Is Regulating the Transition to Postembryonic Development in .
G3 (Bethesda). 2017 Feb 9;7(2):343-353. doi: 10.1534/g3.116.037747.
9
Long-term time-lapse microscopy of C. elegans post-embryonic development.
Nat Commun. 2016 Aug 25;7:12500. doi: 10.1038/ncomms12500.
10
Untwisting the Caenorhabditis elegans embryo.
Elife. 2015 Dec 3;4:e10070. doi: 10.7554/eLife.10070.

本文引用的文献

1
The C. elegans sex-determining gene fem-2 encodes a putative protein phosphatase.
Mol Biol Cell. 1995 Sep;6(9):1159-71. doi: 10.1091/mbc.6.9.1159.
2
ACeDB and macace.
Methods Cell Biol. 1995;48:583-605.
4
Two types of sites required for meiotic chromosome pairing in Caenorhabditis elegans.
Genetics. 1993 Jul;134(3):749-68. doi: 10.1093/genetics/134.3.749.
5
Cell fusions in the developing epithelial of C. elegans.
Dev Biol. 1994 Feb;161(2):408-24. doi: 10.1006/dbio.1994.1041.
7
Identification of genomic regions required for DNA replication during Drosophila embryogenesis.
Genetics. 1993 Nov;135(3):817-29. doi: 10.1093/genetics/135.3.817.
9
Control of cell fates in the central body region of C. elegans by the homeobox gene lin-39.
Cell. 1993 Jul 16;74(1):43-55. doi: 10.1016/0092-8674(93)90293-y.
10
Redundant functions of the genes knirps and knirps-related for the establishment of anterior Drosophila head structures.
Proc Natl Acad Sci U S A. 1994 Aug 30;91(18):8567-71. doi: 10.1073/pnas.91.18.8567.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验