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小鼠原肠胚形成过程中Zic2和Zic3的重叠及不同表达域

Overlapping and distinct expression domains of Zic2 and Zic3 during mouse gastrulation.

作者信息

Elms Paul, Scurry Andrew, Davies Jennifer, Willoughby Catherine, Hacker Terry, Bogani Debora, Arkell Ruth

机构信息

Laboratory of Early Development, Mammalian Genetics Unit, MRC Harwell, Oxfordshire OX11 0RD, UK.

出版信息

Gene Expr Patterns. 2004 Sep;4(5):505-11. doi: 10.1016/j.modgep.2004.03.003.

Abstract

The Zic genes are the vertebrate homologues of the Drosophila Odd-paired gene. Mutations in two of these genes are associated with human congenital genetic disorders. Mutation of human and mouse Zic2 is associated with holoprosencephaly which is caused by a defect of ventral forebrain development and mutation of human and mouse Zic3 is associated with a X-linked heterotaxy syndrome that results from a failure of left-right axis formation. The embryological role of the Zic genes in these disorders is not well understood. Here we show that both of these genes are expressed prior to and throughout gastrulation. The genes show some broad similarities in their expression domains. Both genes however are also uniquely expressed in some tissues and these unique domains correlate with regions that potentially play a role in the aetiology of the respective genetic disorders. During primitive streak stages Zic2 is expressed transiently and uniquely in the node and the head process mesendoderm. The head process is known to be required for the establishment or maintenance of the ventral forebrain, which is the region disrupted in holoprosencephaly. Zic3 is not expressed in the node during primitive streak stages but is expressed in and around the node beginning from the head fold stages of development. This expression of Zic3 correlates well with the first steps in the establishment of the left-right axis. We also examined the expression of the closely related gene, Zic1, and did not detect any transcripts in gastrulation stage embryos.

摘要

Zic基因是果蝇Odd-paired基因在脊椎动物中的同源物。其中两个基因的突变与人类先天性遗传疾病相关。人类和小鼠Zic2的突变与前脑无裂畸形有关,该疾病由腹侧前脑发育缺陷引起;人类和小鼠Zic3的突变与X连锁内脏异位综合征有关,该综合征是由左右轴形成失败导致的。Zic基因在这些疾病中的胚胎学作用尚未完全了解。在此我们表明,这两个基因在原肠胚形成之前及整个过程中均有表达。它们在表达结构域上表现出一些广泛的相似性。然而,这两个基因也在某些组织中独特表达,这些独特的结构域与可能在各自遗传疾病病因学中起作用的区域相关。在原条期,Zic2在原结和头突中胚层短暂且独特地表达。已知头突对于腹侧前脑的建立或维持是必需的,而腹侧前脑正是前脑无裂畸形中受到破坏的区域。在原条期,Zic3在原结中不表达,但从发育的头褶期开始在原结及其周围表达。Zic3的这种表达与左右轴建立的最初步骤密切相关。我们还检测了密切相关的基因Zic1的表达,在原肠胚期胚胎中未检测到任何转录本。

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