An exon encoding the mouse growth hormone binding protein (mGHBP) carboxy terminus is located between exon 7 and 8 of the mouse growth hormone receptor gene.

Receptor Pub Date : 1994-01-01
Y Zhou, L He, J J Kopchick
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Abstract

A C57 black/6 mouse genomic library was screened for mGHR/BP using a mGHR cDNA hybridization probe. Two clones (mGHR-GA and mGHR-GB) were isolated. mGHR-GA contained an insert of 16 kb and hybridized only to exon 4 whereas mGHR-GB possessed an insert of 20 kb and hybridized to exons 6-10 of the mGHR cDNA. Oligonucleotide sequencing analysis confirmed that the mGHR-GA contained exon 4 and that the mGHR-GB possessed mGHR/BP genomic sequences from intron V through the 3' region of mGHR. In addition, mGHR-GB also contained a region, designated exon 8A, encoding the carboxy terminus of mGHBP. This exon is located between exons 7 and 8 of mGHR/BP gene. Two poly(A) additional signal sequences were found 54 bp downstream of the stop codon of mGHBP. Additionally, introns between exons 3/4 and 4/5 are > 12 and > 3 kb, respectively. Also, introns between exons 5/6, 6/7, 7/8A, 8A/8 (3' region of mGHBP), 8/9, 9/10, and the 3' region of mGHR are approx > 3 kb, 4 kb, 287 bp, 1569 bp, 6 kb, 265 bp, and > 3 kb, respectively. This study supports the hypothesis that mGHBP is generated by alternative splicing of a common primary mGHR transcript. It also demonstrates differences and similarities between mGHR/BP and hGHR genes.

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编码小鼠生长激素结合蛋白(mGHBP)羧基末端的外显子位于小鼠生长激素受体基因的外显子7和8之间。
采用mGHR cDNA杂交探针对C57黑/6小鼠基因组文库进行mGHR/BP基因筛选。分离到两个克隆(mGHR-GA和mGHR-GB)。mGHR- ga含有16 kb的插入片段,仅与外显子4杂交,而mGHR- gb含有20 kb的插入片段,与mGHR cDNA的6-10外显子杂交。寡核苷酸测序分析证实,mGHR- ga含有外显子4,mGHR- gb具有从V内含子到mGHR 3'区的mGHR/BP基因组序列。此外,mGHR-GB还含有一个编码mGHBP羧基末端的区域,称为外显子8A。该外显子位于mGHR/BP基因的外显子7和8之间。在mGHBP停止密码子下游54bp处发现两个poly(A)附加信号序列。此外,外显子3/4和4/5之间的内含子分别> 12和> 3 kb。此外,mGHBP的外显子5/6、6/7、7/8A、8A/8 (mGHBP的3'区)、8/9、9/10和mGHR的3'区之间的内含子分别约为> 3 kb、4 kb、287 bp、1569 bp、6 kb、265 bp和> 3 kb。这项研究支持了mGHBP是由一个共同的初级mGHR转录物的选择性剪接产生的假设。同时也显示了mGHR/BP基因与hGHR基因的异同。
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A modeling study of the alpha-subunit of human high-affinity receptor for immunoglobulin-E. Characterization of growth hormone-induced tyrosine-phosphorylated proteins in mouse cells that express GH receptors. Synthetic peptides derived from the steroid binding domain block modulator and molybdate action toward the rat glucocorticoid receptor. Modulation of angiotensin II receptor (AT2) mRNA levels in R3T3 cells. Growth hormone (GH)-induced tyrosine-phosphorylated proteins in cells that express GH receptors.
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