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大鼠L型丙酮酸激酶基因的结构

Structure of the rat L-type pyruvate kinase gene.

作者信息

Cognet M, Lone Y C, Vaulont S, Kahn A, Marie J

机构信息

Unité de Recherches en Génétique et Pathologie Moléculaire, Inserm U. 129, Paris.

出版信息

J Mol Biol. 1987 Jul 5;196(1):11-25. doi: 10.1016/0022-2836(87)90507-9.

Abstract

The total sequence of a 13,021 base-pair (bp) genomic fragment containing the rat L-type pyruvate kinase (L-PK) gene was determined by "shot gun" sequencing. This fragment includes 8360 bp of the L-PK gene, plus 3193 bp of the 5'-flanking and 1468 bp of the 3'-flanking regions. Like the chicken PK-M1 gene, the rat L-PK gene exhibits a fully conserved exon-intron structure, with 11 exons and 10 introns. In the chicken M1 gene, the coding sequences are well conserved (about 70%), in particular at the level of the exons implicated in the formation of PK active sites, exons that are also partially homologous to the corresponding sequences of the yeast gene. Various types of repetitive sequences exist in the L-PK gene, especially two ID (identifier) sequences located in the second intron and the 11th exon. Elements very similar to the "cyclic AMP-dependent regulatory element" recently described in the phosphoenolpyruvate carboxykinase and somatostatin genes are found in the sequenced fragment, but far upstream (-2338) and downstream (+5788) from the cap site. Various sequences homologous to described regulatory elements (glucocorticoid regulatory elements, enhancers, potential Z-DNA) are also observed 5' and 3' of the cap site. A comparison of the 5'-flanking region of the L-PK gene with the same regions of liver-specific or non-specific, cyclic-AMP-responsive or non-responsive genes was also made. It revealed various potentially interesting features that will be used to guide a further functional study. The cap site was determined by primer extension and nuclease S1 mapping using either mature mRNA or precursor RNA as templates. With both templates the start site of transcription appeared to be microheterogeneous, 19 to 14 bp before the ATG translation initiation codon.

摘要

通过“鸟枪法”测序确定了包含大鼠L型丙酮酸激酶(L-PK)基因的13021个碱基对(bp)基因组片段的完整序列。该片段包括L-PK基因的8360 bp,加上5'侧翼的3193 bp和3'侧翼区域的1468 bp。与鸡PK-M1基因一样,大鼠L-PK基因具有完全保守的外显子-内含子结构,有11个外显子和10个内含子。在鸡M1基因中,编码序列保守性良好(约70%),特别是在与PK活性位点形成相关的外显子水平,这些外显子也与酵母基因的相应序列部分同源。L-PK基因中存在各种类型的重复序列,尤其是位于第二个内含子和第11个外显子中的两个ID(标识符)序列。在测序片段中发现了与最近在磷酸烯醇丙酮酸羧激酶和生长抑素基因中描述的“环磷酸腺苷依赖性调节元件”非常相似的元件,但位于帽位点上游很远(-2338)和下游(+5788)。在帽位点的5'和3'也观察到了与所述调节元件(糖皮质激素调节元件、增强子、潜在Z-DNA)同源的各种序列。还对L-PK基因的5'侧翼区域与肝脏特异性或非特异性、环磷酸腺苷反应性或非反应性基因的相同区域进行了比较。结果揭示了各种潜在有趣的特征,将用于指导进一步的功能研究。通过使用成熟mRNA或前体RNA作为模板进行引物延伸和核酸酶S1图谱分析来确定帽位点。使用两种模板时,转录起始位点似乎存在微异质性,在ATG翻译起始密码子之前19至14 bp。

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