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cdh-3是一种编码钙黏蛋白超家族成员的基因,在秀丽隐杆线虫的上皮细胞形态发生中发挥作用。

cdh-3, a gene encoding a member of the cadherin superfamily, functions in epithelial cell morphogenesis in Caenorhabditis elegans.

作者信息

Pettitt J, Wood W B, Plasterk R H

机构信息

Division of Molecular Biology, The Netherlands Cancer Institute, Amsterdam.

出版信息

Development. 1996 Dec;122(12):4149-57. doi: 10.1242/dev.122.12.4149.

Abstract

Several genes that encode members of the cadherin superfamily have been identified in Caenorhabditis elegans. Based on the roles of cadherins in vertebrates and Drosophila, it is expected that they function in the control of epithelial morphogenesis, an event which is poorly understood at the molecular level in C. elegans. Reporter genes under the control of upstream sequences from one of these genes, cdh-3, are expressed in developing epithelial cells, but also in a number of neuroectodermal cells that extend processes along some of these epithelial cells. We generated a loss-of-function mutation in cdh-3 by transposon-mediated deletion mutagenesis. This mutation affects the morphogenesis of a single cell, hyp10, which forms the tip of the nematode tail. The lack of detectable defects associated with the other cells expressing cdh-3 reporter constructs hints at the existence of other genes that can compensate for cdh-3 loss of function.

摘要

在秀丽隐杆线虫中已鉴定出几个编码钙黏蛋白超家族成员的基因。基于钙黏蛋白在脊椎动物和果蝇中的作用,可以预期它们在控制上皮形态发生中发挥作用,而这一事件在秀丽隐杆线虫的分子水平上了解甚少。在其中一个基因cdh-3的上游序列控制下的报告基因,在发育中的上皮细胞中表达,但也在一些沿着这些上皮细胞延伸突起的神经外胚层细胞中表达。我们通过转座子介导的缺失诱变在cdh-3中产生了功能缺失突变。这种突变影响单个细胞hyp10的形态发生,hyp10形成线虫尾部的尖端。与表达cdh-3报告构建体的其他细胞相关的可检测缺陷的缺乏暗示了存在其他可以补偿cdh-3功能丧失的基因。

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