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秀丽隐杆线虫胚胎发育过程中皮下细胞和神经胶质样细胞发育所需基因座的筛选。

A screen for genetic loci required for hypodermal cell and glial-like cell development during Caenorhabditis elegans embryogenesis.

作者信息

Chanal P, Labouesse M

机构信息

Institut de Génétìque et de Biologie Moléculaire et Cellulairs, Illkirch, France.

出版信息

Genetics. 1997 May;146(1):207-26. doi: 10.1093/genetics/146.1.207.

Abstract

The Caenorhabditis elegans lin-26 gene is expressed in all nonneuronal ectodermal cells. To identify genes required to specify the fates of ectodermal cells, we have conducted screens designed to identify loci whose zygotic function would be required for normal lin-26 expression. First, we examined 90 deficiencies covering 75% of the genome; second, we examined the progeny of 3600 genomes after EMS mutagenesis. We identified six loci that appear to be required for normal lin-26 expression. We argue that the deficiency eDf19 deletes a gene involved in specifying hypodermal cell fates. The genes emb-29 (previously known) and ale-1 (newly found) could be involved in a cell cycle function and/or in specifying the fates of some precursors within different lineages that generate hypodermal cells and nonectodermal cells. We argue that the overlapping deficiencies qDf7, qDf8 and qDf9 delete a gene required to limit the number of nonneuronal ectodermal cells. We suggest that the deficiencies ozDf2, itDf2 and nDf42 delete genes required, directly or indirectly, to repress lin-26 expression in cells that normally do not express lin-26. We discuss the implications of these findings concerning the generation of the ectoderm.

摘要

秀丽隐杆线虫的lin-26基因在所有非神经外胚层细胞中表达。为了鉴定决定外胚层细胞命运所需的基因,我们进行了筛选,旨在鉴定其合子功能对正常lin-26表达必不可少的基因座。首先,我们检测了覆盖75%基因组的90个缺失;其次,我们检测了EMS诱变后3600个基因组的后代。我们鉴定出六个似乎是正常lin-26表达所必需的基因座。我们认为缺失eDf19删除了一个参与决定皮下细胞命运的基因。基因emb-29(先前已知)和ale-1(新发现)可能参与细胞周期功能和/或决定产生皮下细胞和非外胚层细胞的不同谱系中一些前体细胞的命运。我们认为重叠缺失qDf7、qDf8和qDf9删除了一个限制非神经外胚层细胞数量所需的基因。我们认为缺失ozDf2、itDf2和nDf42删除了直接或间接在正常不表达lin-26的细胞中抑制lin-26表达所需的基因。我们讨论了这些发现对外胚层产生的影响。

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