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影响斑马鱼原肠胚形成过程中细胞命运和细胞重排的突变

Mutations affecting cell fates and cellular rearrangements during gastrulation in zebrafish.

作者信息

Solnica-Krezel L, Stemple D L, Mountcastle-Shah E, Rangini Z, Neuhauss S C, Malicki J, Schier A F, Stainier D Y, Zwartkruis F, Abdelilah S, Driever W

机构信息

Cardiovascular Research Center, Massachusetts General Hospital, Charlestown 02129, USA.

出版信息

Development. 1996 Dec;123:67-80. doi: 10.1242/dev.123.1.67.

Abstract

One of the major challenges of developmental biology is understanding the inductive and morphogenetic processes that shape the vertebrate embryo. In a large-scale genetic screen for zygotic effect, embryonic lethal mutations in zebrafish we have identified 25 mutations that affect specification of cell fates and/or cellular rearrangements during gastrulation. These mutations define at least 14 complementation groups, four of which correspond to previously identified genes. Phenotypic analysis of the ten novel loci revealed three groups of mutations causing distinct effects on cell fates in the gastrula. One group comprises mutations that lead to deficiencies in dorsal mesodermal fates and affect central nervous system patterning. Mutations from the second group affect formation of ventroposterior embryonic structures. We suggest that mutations in these two groups identify genes necessary for the formation, maintenance or function of the dorsal organizer and the ventral signaling pathway, respectively. Mutations in the third group affect primarily cellular rearrangements during gastrulation and have complex effects on cell fates in the embryo. This group, and to some extent mutations from the first two groups, affect the major morphogenetic processes, epiboly, convergence and extension, and tail morphogenesis. These mutations provide an approach to understanding the genetic control of gastrulation in vertebrates.

摘要

发育生物学的主要挑战之一是理解塑造脊椎动物胚胎的诱导和形态发生过程。在一项针对合子效应的大规模遗传筛选中,我们在斑马鱼中鉴定出25个影响原肠胚形成期间细胞命运特化和/或细胞重排的胚胎致死突变。这些突变定义了至少14个互补群,其中四个对应于先前鉴定的基因。对十个新基因座的表型分析揭示了三组对原肠胚细胞命运产生不同影响的突变。一组包括导致背侧中胚层命运缺陷并影响中枢神经系统模式形成的突变。第二组的突变影响胚胎腹侧后部结构的形成。我们认为,这两组突变分别鉴定了背侧组织者和腹侧信号通路形成、维持或功能所必需的基因。第三组的突变主要影响原肠胚形成期间的细胞重排,并对胚胎中的细胞命运产生复杂影响。这一组,以及在某种程度上来自前两组的突变,影响主要的形态发生过程,外包、汇聚延伸和尾部形态发生。这些突变提供了一种理解脊椎动物原肠胚形成遗传控制的方法。

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