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一个编码假定富含脯氨酸嵌合细胞壁蛋白的盐诱导苜蓿基因的转录后调控

Post-transcriptional regulation of a salt-inducible alfalfa gene encoding a putative chimeric proline-rich cell wall protein.

作者信息

Deutch C E, Winicov I

机构信息

Department of Biochemistry, University of Nevada, Reno 89557.

出版信息

Plant Mol Biol. 1995 Jan;27(2):411-8. doi: 10.1007/BF00020194.

Abstract

A cDNA previously shown to identify a salt-inducible root-specific transcript in Medicago sativa was used to screen an alfalfa library for the corresponding genomic sequence. One positive clone was recovered. The nucleotide sequence of a subclone contained a 329 bp 5' region upstream of the first ATG codon, a 1143 bp coding segment, and a 447 bp 3'-untranslated region interrupted by a single 475 bp intron. Translation of the coding segment, which was designated MsPRP2, suggested it encodes a chimeric 40,569 Da cell wall protein with an amino-terminal signal sequence, a repetitive proline-rich sequence, and a cysteine-rich carboxyl-terminal sequence homologous to nonspecific lipid transfer proteins. The 3'-untranslated region of MsPRP2 contained a sequence similar to one found to destabilize mRNAs transcribed from the elicitor-regulated proline-rich protein gene PvPRP1. Transcription run-on experiments using nuclei from salt-sensitive and salt-tolerant alfalfa callus suggested that the accumulation of MsPRP2 transcripts in salt-tolerant alfalfa cells grown in the presence of salt is due primarily to increased mRNA stability. The MsPRP2 gene thus may be a useful model for studying post-transcriptional salt-regulated expression of cell wall proteins.

摘要

一个先前已被证明可识别紫花苜蓿中盐诱导的根特异性转录本的cDNA,被用于筛选苜蓿文库以寻找相应的基因组序列。获得了一个阳性克隆。一个亚克隆的核苷酸序列包含第一个ATG密码子上游329 bp的5'区域、一个1143 bp的编码区段以及一个447 bp的3'-非翻译区,该非翻译区被一个475 bp的单一内含子打断。被命名为MsPRP2的编码区段的翻译表明,它编码一种嵌合的40,569 Da细胞壁蛋白,该蛋白具有一个氨基末端信号序列、一个富含脯氨酸的重复序列以及一个与非特异性脂质转移蛋白同源的富含半胱氨酸的羧基末端序列。MsPRP2的3'-非翻译区包含一个与从激发子调控的富含脯氨酸蛋白基因PvPRP1转录的mRNA去稳定化序列相似的序列。使用来自盐敏感和耐盐苜蓿愈伤组织的细胞核进行的转录连续实验表明,在盐存在下生长的耐盐苜蓿细胞中MsPRP2转录本的积累主要是由于mRNA稳定性增加。因此,MsPRP2基因可能是研究细胞壁蛋白转录后盐调控表达的有用模型。

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