Moffat J G, Edens A, Talamantes F
Department of Biology, University of California, Santa Cruz, California 95060, USA.
J Mol Endocrinol. 1999 Aug;23(1):33-44. doi: 10.1677/jme.0.0230033.
The mouse growth hormone receptor/growth hormone-binding protein (GHR/BP) gene produces several distinct mRNA forms through alternative splicing, including mRNAs encoding the membrane-bound growth hormone receptor (GHR) and the soluble growth hormone-binding protein (GHBP). Transcripts are also heterogeneous in their 5' regions due to alternative selection of two major 5' untranslated region (5'UTR) sequences, designated L1 and L2. Here we report the cloning of all mouse GHR/BP coding exons as well as the exon encoding 5'UTR L2, the most widely expressed 5'UTR. The mouse GHR/GHBP gene contains 11 coding exons, 9 of which are homologous in size and sequence to human GHR exons 2-10. The two mouse exons that do not have homologs in the human gene are designated exons 4B and 8A. Exon 4B, located between exons 4 and 5, encodes an 8-amino acid segment of the ligand binding domain that is unique to mouse GHR and GHBP. Analysis by reverse transcriptase-polymerase chain reaction indicated that exon 4B is constitutively present in mouse GHR and GHBP mRNA. Exon 8A encodes the GHBP hydrophilic tail and 3'UTR sequence. 5'UTR L2 is encoded by a single exon located at least 27 kb upstream of exon 2 and at least 12 kb upstream of the exon encoding 5'UTR L1. The transcription start sites of UTR L2 were mapped and the 5' flanking region sequenced. The exon and proximal promoter region are GC rich, and share a high level of conservation with the equivalent exons in the sheep, bovine and human GHR genes. A CCAAT motif and several putative Sp1 motifs are present, and there is no TATA box. Homology between the mouse sequence and other species is limited to a region of 450 bp upstream of the exon due to the insertion of a fragment of a LINE-1 element upstream of the mouse L2 exon. Ribonuclease protection assays were used to confirm that 5'UTR L2 is widely expressed in multiple tissues and is the predominant form of transcript except in the liver during pregnancy, in which 5'UTR L1 is the major form.
小鼠生长激素受体/生长激素结合蛋白(GHR/BP)基因通过可变剪接产生几种不同的mRNA形式,包括编码膜结合生长激素受体(GHR)和可溶性生长激素结合蛋白(GHBP)的mRNA。由于两种主要的5'非翻译区(5'UTR)序列(称为L1和L2)的可变选择,转录本在其5'区域也具有异质性。在此,我们报道了所有小鼠GHR/BP编码外显子以及编码5'UTR L2(表达最广泛的5'UTR)的外显子的克隆。小鼠GHR/GHBP基因包含11个编码外显子,其中9个在大小和序列上与人类GHR外显子2 - 10同源。在人类基因中没有同源物的两个小鼠外显子被命名为外显子4B和8A。位于外显子4和5之间的外显子4B编码配体结合结构域的一个8氨基酸片段(这是小鼠GHR和GHBP所特有的)。逆转录 - 聚合酶链反应分析表明外显子4B在小鼠GHR和GHBP mRNA中持续存在。外显子8A编码GHBP亲水性尾部和3'UTR序列。5'UTR L2由位于外显子2上游至少27 kb且位于编码5'UTR L1的外显子上游至少12 kb的单个外显子编码。绘制了UTR L2的转录起始位点并对5'侧翼区域进行了测序。该外显子和近端启动子区域富含GC,并且与绵羊、牛和人类GHR基因中的等效外显子具有高度保守性。存在一个CCAAT基序和几个推定的Sp1基序,并且没有TATA框。由于在小鼠L2外显子上游插入了一个LINE - 1元件片段,小鼠序列与其他物种之间的同源性仅限于该外显子上游450 bp的区域。核糖核酸酶保护分析用于确认5'UTR L2在多种组织中广泛表达,并且是转录本的主要形式,除了在怀孕期间的肝脏中,其中5'UTR L1是主要形式。