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一个具有修饰C末端的PMR2串联重复序列位于酿酒酵母中编码赖氨酰-tRNA合成酶的KRS1基因下游。

A PMR2 tandem repeat with a modified C-terminus is located downstream from the KRS1 gene encoding lysyl-tRNA synthetase in Saccharomyces cerevisiae.

作者信息

Martinez R, Latreille M T, Mirande M

机构信息

Laboratoire d'Enzymologie, Centre National de la Recherche Scientifique, Gif-sur-Yvette, France.

出版信息

Mol Gen Genet. 1991 May;227(1):149-54. doi: 10.1007/BF00260720.

Abstract

The KRS1 gene encodes the cytoplasmic form of Saccharomyces cerevisiae lysyl-tRNA synthetase. The KRS1 locus has been characterized. The lysyl-tRNA synthetase gene is unique in the yeast genome. The gene is located on the right arm of chromosome IV and disruption of the open reading frame leads to lethality. These results contrast with the situation encountered in Escherichia coli where lysyl-tRNA synthetase is coded by two distinct genes, lysS and lysU, and further address the possible biological significance of this gene duplication. The nucleotide sequence of the 3'-flanking region has been established. It encodes a long open reading frame whose nucleotide and amino acid structures are almost identical to PMR2, a cluster of tandemly repeated genes coding for P-type ion pumps. The sequence alterations relative to PMR2 are mainly located at the C-terminus of the protein.

摘要

KRS1基因编码酿酒酵母赖氨酰 - tRNA合成酶的胞质形式。KRS1基因座已被鉴定。赖氨酰 - tRNA合成酶基因在酵母基因组中是独特的。该基因位于第四条染色体的右臂上,开放阅读框的破坏会导致致死性。这些结果与大肠杆菌中的情况形成对比,在大肠杆菌中赖氨酰 - tRNA合成酶由两个不同的基因lysS和lysU编码,并且进一步探讨了这种基因重复可能的生物学意义。已确定了3'侧翼区域的核苷酸序列。它编码一个长的开放阅读框,其核苷酸和氨基酸结构与PMR2几乎相同,PMR2是一组编码P型离子泵的串联重复基因。相对于PMR2的序列改变主要位于蛋白质的C末端。

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