Developmental Plasticity and Cellular Reprogramming in Caenorhabditis elegans

被引:21
|
作者
Rothman, Joel [1 ,2 ]
Jarriault, Sophie [3 ]
机构
[1] Univ Calif Santa Barbara, Dept MCD Biol, Santa Barbara, CA 93111 USA
[2] Univ Calif Santa Barbara, Neurosci Res Inst, Santa Barbara, CA 93111 USA
[3] Univ Strasbourg, Inserm U1258, CNRS UMR7104, Dept Dev & Stem Cells,IGBMC, 1 Rue Laurent Fries,BP10142, F-67404 Illkirch Graffenstaden, France
基金
欧洲研究理事会; 美国国家卫生研究院;
关键词
reprogramming; transdifferentiation; transdetermination; cell type conversion; stem cells; WormBook; REPRESSIVE COMPLEX 2; KH DOMAIN PROTEIN; C-ELEGANS; GENE-EXPRESSION; SELF-RENEWAL; TRANSCRIPTION FACTORS; DIRECT CONVERSION; STEM-CELLS; EPIGENETIC MEMORY; MOUSE FIBROBLASTS;
D O I
10.1534/genetics.119.302333
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
While Caenorhabditis elegans was originally regarded as a model for investigating determinate developmental programs, landmark studies have subsequently shown that the largely invariant pattern of development in the animal does not reflect irreversibility in rigidly fixed cell fates. Rather, cells at all stages of development, in both the soma and germline, have been shown to be capable of changing their fates through mutation or forced expression of fate-determining factors, as well as during the normal course of development. In this chapter, we review the basis for natural and induced cellular plasticity in C. elegans. We describe the events that progressively restrict cellular differentiation during embryogenesis, starting with the multipotency-to-commitment transition (MCT) and subsequently through postembryonic development of the animal, and consider the range of molecular processes, including transcriptional and translational control systems, that contribute to cellular plasticity. These findings in the worm are discussed in the context of both classical and recent studies of cellular plasticity in vertebrate systems.
引用
收藏
页码:723 / 757
页数:35
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