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酵母核糖体蛋白L32及其基因。

The yeast ribosomal protein L32 and its gene.

作者信息

Dabeva M D, Warner J R

机构信息

Department of Cell Biology, Albert Einstein College of Medicine, Bronx, New York 10461.

出版信息

J Biol Chem. 1987 Nov 25;262(33):16055-9.

PMID:3316213
Abstract

The yeast ribosomal protein gene RPL32 of Saccharomyces cerevisiae is of particular interest for two reasons: 1) it is adjacent to another ribosomal protein gene, RP29, whose divergent transcription may be driven from the same control sequences, and 2) it appears that the splicing of its transcript is regulated by the product of the gene, ribosomal protein in L32. RPL32 has been analyzed in detail. It is essential for cell growth. Its sequence predicts L32 to be a protein of 105 amino acids, somewhat basic near the NH2 terminus, rather acidic near the COOH terminus, and homologous to ribosomal protein L30 of mammals. The reading frame has been confirmed by partial NH2-terminal analysis of L32. The nucleotide sequence also predicts an intron of 230 nucleotides, which begins with the unusual sequence GTCAGT and ends 40 nucleotides downstream of the consensus sequence TAC-TAAC. The intron has been confirmed by determination of the sequence of a cDNA clone. Transcription initiates 58 nucleotides upstream of the AUG initiation codon, and the polyadenylation site occurs 100 nucleotides downstream of the termination codon. Regulation of the transcription of ribosomal protein genes has been linked to two related consensus sequences. Analysis of the intergenic region between RP29 and RPL32 reveals three copies of these sequences. A deletion removing all three sequences reduces synthesis of a L32-LacZ fusion protein by more than 90%. Some residual activity, however, remains.

摘要

酿酒酵母的酵母核糖体蛋白基因RPL32之所以特别受关注,有两个原因:1)它与另一个核糖体蛋白基因RP29相邻,其不同的转录可能由相同的控制序列驱动;2)其转录本的剪接似乎受该基因产物核糖体蛋白L32的调控。RPL32已得到详细分析。它对细胞生长至关重要。其序列预测L32是一种含105个氨基酸的蛋白质,在NH2末端附近略显碱性,在COOH末端附近相当酸性,并且与哺乳动物的核糖体蛋白L30同源。L32的部分NH2末端分析已证实了阅读框。核苷酸序列还预测有一个230个核苷酸的内含子,其起始序列为不寻常的GTCAGT,在共有序列TAC-TAAC下游40个核苷酸处结束。通过测定cDNA克隆的序列已证实了该内含子。转录在AUG起始密码子上游58个核苷酸处起始,聚腺苷酸化位点在终止密码子下游100个核苷酸处。核糖体蛋白基因转录的调控与两个相关的共有序列有关。对RP29和RPL32之间基因间区域的分析揭示了这些序列的三个拷贝。删除所有这三个序列会使L32-LacZ融合蛋白的合成减少90%以上。然而,仍有一些残余活性。

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