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[斑马鱼leg1同源基因mu-leg1在小鼠中的表达模式分析]

[Analysis of expression pattern of zebrafish leg1 homologus gene mu-leg1 in mouse].

作者信息

Zhu Zhi-Hui, Hu Min-Jie, Chang Chang-Qing, Peng Jin-Rong

机构信息

College of Animal Sciences, ZhejiangUniversity, Hangzhou 310058, China.

出版信息

Yi Chuan. 2012 Sep;34(9):1174-80.

Abstract

Gene leg1 (liver-enriched gene 1) was first identified as a novel gene whose expression was enriched in the liver of zebrafish. Further studies revealed that Leg1 protein was a novel secretory protein, which played a role in the liver development in zebrafish. Here we reported the analysis of expression pattern of zb-leg1 homologus gene mu-leg1. The cDNA of mu-leg1 was isolated from adult mouse liver by nested PCR. This gene encodes a putative protein, mu-Leg1, which shares 31% similarity with zb-Leg1 of zebrafish. Both Northern blotting and semi-quantitative RT-PCR demonstrated that the expression of mu-leg1 was enriched in the small intestine rather than in the liver in adult mouse. We also produced a recombined mu-Leg1 protein and a mu-Leg1 specific antibody. Western blottingdemonstrated that mu-Leg1 was a secretory protein. In addition, we have established a mu-leg1 conditional knock-out heterozygous mouse. Our work builds a basis for further studies of mu-leg1.

摘要

基因leg1(肝脏富集基因1)最初被鉴定为一种在斑马鱼肝脏中表达丰富的新基因。进一步研究表明,Leg1蛋白是一种新型分泌蛋白,在斑马鱼肝脏发育中发挥作用。在此,我们报告了对zb-leg1同源基因mu-leg1表达模式的分析。通过巢式PCR从成年小鼠肝脏中分离出mu-leg1的cDNA。该基因编码一种假定的蛋白mu-Leg1,它与斑马鱼的zb-Leg1具有31%的相似性。Northern印迹法和半定量RT-PCR均表明,在成年小鼠中,mu-leg1的表达在小肠中丰富,而不是在肝脏中。我们还制备了重组mu-Leg1蛋白和mu-Leg1特异性抗体。蛋白质免疫印迹法表明mu-Leg1是一种分泌蛋白。此外,我们建立了mu-leg1条件性敲除杂合小鼠。我们的工作为进一步研究mu-leg1奠定了基础。

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