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文昌鱼和斑马鱼 Smad 核相互作用蛋白 1 的独特基因结构和表达模式。

Distinct gene structure and expression pattern of Smad nuclear interacting protein 1 in amphioxus and zebrafish.

机构信息

Institute of Developmental Biology, School of Life Sciences, National Key Laboratory of Experimental Teratology, Shandong University, Jinan, China.

出版信息

Acta Histochem. 2012 Jul;114(4):386-91. doi: 10.1016/j.acthis.2011.07.007. Epub 2011 Aug 9.

Abstract

A Smad nuclear interacting protein 1 (SNIP1) homologous gene was identified in amphioxus. Phylogenic analysis showed that SNIP1 proteins from different species share a highly conserved FHA domain at the C-terminus, but their N-terminus varies remarkably. The genomic structure of SNIP1 varies in different species, especially at the 5' end. Through in situ hybridization, we studied SNIP1 expression patterns in amphioxus and zebrafish embryos. Amphioxus SNIP1 transcripts were specifically located in the notochord in larval and adult stages. In zebrafish, however, snip1 transcripts were specifically located not only in the notochord, but also in the rhombencephalic ventricle, otic vesicles and pectoral fin buds. This is the first report of SNIP1 expression pattern in early development, which clearly shows different expression patterns between invertebrates and vertebrates. Previous studies reported that it is the N-terminal domain of human and mouse SNIP1 that functions to inhibit both TGF-ß and the NF-κB pathways. Therefore, it is most likely that the modification of SNIP1 expression pattern is related to the remarkable evolution in the N-terminal sequence. In addition, the difference in SNIP1 expression pattern between amphioxus and zebrafish implies the role of SNIP1 in the vertebrate body structural innovation of brain, otic vesicles and pectoral fins.

摘要

在文昌鱼中鉴定出一个 Smad 核相互作用蛋白 1 (SNIP1) 同源基因。系统发育分析表明,不同物种的 SNIP1 蛋白在 C 端具有高度保守的 FHA 结构域,但它们的 N 端差异显著。SNIP1 的基因组结构在不同物种中存在差异,尤其是在 5'端。通过原位杂交,我们研究了 SNIP1 在文昌鱼和斑马鱼胚胎中的表达模式。文昌鱼 SNIP1 转录本在幼虫和成体阶段特异性定位于脊索。然而,在斑马鱼中,snip1 转录本不仅特异性定位于脊索,还特异性定位于后脑室、耳泡和胸鳍芽。这是首次报道 SNIP1 在早期发育中的表达模式,清楚地显示了无脊椎动物和脊椎动物之间的不同表达模式。先前的研究报告称,正是人源和鼠源 SNIP1 的 N 端结构域起作用,同时抑制 TGF-β和 NF-κB 通路。因此,SNIP1 表达模式的修饰很可能与 N 端序列的显著进化有关。此外,文昌鱼和斑马鱼之间 SNIP1 表达模式的差异暗示了 SNIP1 在脑、耳泡和胸鳍等脊椎动物身体结构创新中的作用。

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