首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Cloning expression and in situ localization of rat intestinal cGMP-dependent protein kinase II.
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Cloning expression and in situ localization of rat intestinal cGMP-dependent protein kinase II.

机译:大鼠肠道cGMP依赖性蛋白激酶II的克隆表达和原位定位。

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摘要

The cDNA for a membrane-associated cGMP-dependent protein kinase (cGK II) was cloned from rat intestine using reverse transcriptase PCR and oligonucleotide primers encoding two conserved motifs of known cGMP-dependent protein kinases and subsequently by screening a rat intestine cDNA library. A full-length clone encodes a protein of 761 amino acids with an estimated size of 87 kDa. Sequences of eight peptides from purified pig intestinal mucosa cGK II were found in the derived amino acid sequence of this clone, identifying it as rat intestinal cGK II. Phylogenetic analysis showed that rat intestinal cGK II is less related to mammalian cGK I than to the Drosophila DG1 gene product and most closely related to a recently cloned mouse brain CGKII isoform. Like several other cGK sequences, that of cGK II contained a leucine/isoleucine heptad repeat motif that has been implicated in dimer formation in cGK I. Expression of cGK II cDNA in HEK 293 cells followed by subcellular fractionation revealed cGK II localization in the cell particulate fraction, consistent with the membrane association of endogenous rat cGK II. On Northern blots, the major cGK II poly(A) RNA form was 4.8 kb, with minor forms of 6.2 and 3.1 kb. The cGK II RNA was highly expressed in rat intestinal mucosa and was 20 times less abundant in rat brain and kidney. The localization of endogenous cGK II RNA in rat small intestine was shown by in situ hybridization to be in villous epithelial cells and to some extent in crypt cells.
机译:使用逆转录酶PCR和编码已知cGMP依赖性蛋白激酶的两个保守基序的寡核苷酸引物,从大鼠肠中克隆出与膜相关的cGMP依赖性蛋白激酶(cGK II)的cDNA,随后通过筛选大鼠肠cDNA文库。全长克隆编码一个761个氨基酸的蛋白质,估计大小为87 kDa。在该克隆的衍生氨基酸序列中发现了来自纯化的猪肠粘膜cGK II的八种肽的序列,将其鉴定为大鼠肠cGK II。系统发育分析表明,大鼠肠道cGK II与哺乳动物cGK I的关系比果蝇DG1基因产物少,并且与最近克隆的小鼠大脑CGKII亚型关系最密切。像其他几个cGK序列一样,cGK II包含一个亮氨酸/异亮氨酸七肽重复基序,该基序与cGK I中的二聚体形成有关。在HEK 293细胞中表达cGK II cDNA,然后进行亚细胞分级分离,揭示了cGK II在细胞颗粒中的定位分数,与内源性大鼠cGK II的膜结合一致。在Northern印迹上,主要的cGK II poly(A)RNA形式为4.8 kb,次要形式为6.2和3.1 kb。 cGK II RNA在大鼠肠粘膜中高表达,在大鼠脑和肾中的含量低20倍。通过原位杂交显示内源性cGK II RNA在大鼠小肠中的定位在绒毛上皮细胞中,并在一定程度上在隐窝细胞中。

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