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家蚕新型 BmGDAP1 基因的克隆、鉴定及其在细胞质多角体病毒感染中的表达分析

Cloning, characterization, and expression analysis of a novel BmGDAP1 gene from silkworm, Bombyx mori, involved in cytoplasmic polyhedrosis virus infection.

机构信息

Sericultural Research Institute, Jiangsu University of Science and Technology, Jiangsu, China.

出版信息

Gene. 2012 Apr 15;497(2):208-13. doi: 10.1016/j.gene.2012.01.037. Epub 2012 Jan 30.

Abstract

A novel ganglioside-induced differentiation-associated protein 1 gene (BmGDAP1) was first cloned and sequenced from silkworm, Bombyx mori using rapid amplification of cDNA ends (RACE). The full-length cDNA of BmGDAP1 was 1514bp, consisting of a 91bp 5' untranslated region (UTR), a 424bp 3'-UTR and a 999bp open reading frame (ORF). The ORF encoded a polypeptide of 332 amino acids, which possessed a thioredoxin (TRX)-like domain, a glutathione S-transferase-C (GST-C) family domain and a transmembrane segment. Furthermore, quantitative real-time PCR analysis revealed that BmGDAP1 transcripts were mainly presented in the tissues of hemocytes and midgut of silkworm, and its expression level was down-regulated in the hemocytes, while up-regulated in the midgut. Therefore, it could be concluded that BmGDAP1 plays an important role in the recognition and immune response of silkworm to BmCPV infection.

摘要

我们首次从家蚕(Bombyx mori)中克隆并测序了一个神经节苷脂诱导分化相关蛋白 1 基因(BmGDAP1),采用的方法是快速扩增 cDNA 末端(RACE)。BmGDAP1 的全长 cDNA 为 1514bp,包括一个 91bp 的 5'非翻译区(UTR)、一个 424bp 的 3'UTR 和一个 999bp 的开放阅读框(ORF)。ORF 编码一个 332 个氨基酸的多肽,它具有硫氧还蛋白(TRX)样结构域、谷胱甘肽 S-转移酶-C(GST-C)家族结构域和跨膜片段。此外,实时定量 PCR 分析显示,BmGDAP1 转录本主要存在于家蚕血细胞和中肠组织中,在家蚕血细胞中表达水平下调,而在中肠中上调。因此,可以得出结论,BmGDAP1 在 BmCPV 感染家蚕的识别和免疫反应中发挥重要作用。

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