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在人胰岛中表达的一种截短的钙/钙调蛋白依赖性蛋白激酶II同工型可能是反式剪接的结果。

A truncated isoform of Ca2+/calmodulin-dependent protein kinase II expressed in human islets of Langerhans may result from trans-splicing.

作者信息

Breen M A, Ashcroft S J

机构信息

Nuffield Department of Clinical Biochemistry, John Radcliffe Hospital, Headington, Oxford, UK.

出版信息

FEBS Lett. 1997 Jun 16;409(3):375-9. doi: 10.1016/s0014-5793(97)00555-3.

Abstract

Calcium/calmodulin-dependent protein kinase II (CaM kinase II) has been proposed to play a key role in glucose stimulated insulin secretion. Using the rapid amplification of cDNA ends technique we amplified the 3' end of the CaM kinase II gamma gene from human islet RNA. A novel cDNA was detected composed of 5' sequence from the human CaM kinase II gamma gene joined to the 3' end of the human signal recognition particle 72 (SRP72) gene. We predict that this mRNA species will code for a truncated form of CaM kinase II, designated gammaSRP, comprising the entire catalytic and regulatory domains of the protein and with a predicted molecular weight of 37 kDa. We mapped the human SRP72 gene to chromosome 18 and, as the CaM kinase II gamma gene was previously mapped to human chromosome 10q22, we suggest this novel cDNA may have resulted from trans-splicing.

摘要

钙/钙调蛋白依赖性蛋白激酶II(CaM激酶II)被认为在葡萄糖刺激的胰岛素分泌中起关键作用。我们使用cDNA末端快速扩增技术从人胰岛RNA中扩增出CaM激酶IIγ基因的3'端。检测到一种新的cDNA,它由人CaM激酶IIγ基因的5'序列与人类信号识别颗粒72(SRP72)基因的3'端连接而成。我们预测这种mRNA种类将编码一种截短形式的CaM激酶II,命名为γSRP,它包含该蛋白质的整个催化和调节结构域,预测分子量为37 kDa。我们将人类SRP72基因定位到18号染色体,并且由于CaM激酶IIγ基因先前已定位到人类染色体10q22,我们认为这种新的cDNA可能是由反式剪接产生的。

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