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首页> 外文期刊>Journal of biomedical science. >Cloning, expression and chromosomal localization of human Ca2+/calmodulin-dependent protein kinase kinase.
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Cloning, expression and chromosomal localization of human Ca2+/calmodulin-dependent protein kinase kinase.

机译:人Ca2 + /钙调蛋白依赖性蛋白激酶激酶的克隆,表达和染色体定位。

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摘要

A human cDNA clone encoding the calcium/calmodulin-dependent protein kinase kinase (CaMKK) was isolated by RT-PCR amplification of the fragment corresponding to the conserved kinase catalytic domain followed by rapid amplification of cDNA ends and cDNA library screening. Compilation of nucleotide sequencing data yielded a consensus cDNA sequence of 1.9 kb with an open reading frame of 1,251 nucleotides in length which translates to a polypeptide of 417 amino acids (47 kd). It showed significant homology to the rat brain CaMKK isozymes. The human CaMKK, which was expressed as a Flag-tagged protein in human non-small cell lung cancer H- 1299 cells followed by immunoprecipitation with anti-Flag antibody, was shown to phosphorylate recombinant human CaMK I in a calcium/CaM-dependent fashion. Northern blot analysis revealed that human CaMKK is ubiquitously expressed, with brain showing the highest level of expression. The CaMKK gene is localized to human chromosome 12. The presence of cDNA clones with divergent 3' terminal sequences suggests a family of CaMKK variants which may arise from alternative splicing.
机译:通过RT-PCR扩增对应于保守激酶催化结构域的片段,分离出编码钙/钙调蛋白依赖性蛋白激酶激酶(CaMKK)的人类cDNA克隆,然后快速扩增cDNA末端并筛选cDNA文库。核苷酸测序数据的汇编产生了1.9 kb的共有cDNA序列,其开放阅读框的长度为1,251个核苷酸,可翻译为417个氨基酸(47 kd)的多肽。它显示出与大鼠脑CaMKK同工酶的显着同源性。人类CaMKK被表达为人类非小细胞肺癌H-1299细胞中带有Flag标签的蛋白,然后用抗Flag抗体进行免疫沉淀,被证明以钙/ CaM依赖性方式磷酸化重组人类CaMKI。 。 Northern印迹分析表明,人CaMKK被普遍表达,大脑显示出最高水平的表达。 CaMKK基因位于人类12号染色体上。具有不同3'末端序列的cDNA克隆的存在表明可能由交替剪接产生的CaMKK变体家族。

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