Tsai-Morris C H, Buczko E, Wang W, Xie X Z, Dufau M L
Section on Molecular Endocrinology, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892.
J Biol Chem. 1991 Jun 15;266(17):11355-9.
The luteinizing hormone (LH)/human chorionic gonadotropin (hCG) receptor gene was isolated from rat liver genomic libraries and spanned at least 75 kilobase pairs from nucleotide -2057 of the 5'-flanking region to the 3'-noncoding end. The structural configuration of the coding region of the LH receptor gene consists of 11 exons separated by 10 introns that are all located within the putative extracellular domain prior to the first transmembrane region. The 5'-noncoding region contains several potential TATA boxes and SP1 promoter binding sites, as well as six palindromic elements, potential intron/exon splice junctions, and two extended open reading frames in frame with the initiation codon. Primer extension studies indicate the presence of multiple transcriptional initiation sites. Truncated forms of the LH/hCG receptor conform to alternative splicing patterns that are consistent either with the deletion of complete exons or alternate acceptor sites within exons. All splice site junctions correspond to known donor and acceptor consensus sequences. Exons 2-8 approximate the regions of the 14 consecutive 20 amino acid repeated motifs present in the LH, thyrotropin-stimulating hormone, and follicle-stimulating hormone receptor cDNAs, with the exception of a six to eight amino acid shift in each motif. Exons 1, 9, 10, and 11, do not conform to this repetitive intronic motif. These exons, however, contain important structural elements including the conserved cysteines (exons 1, 9, 11), the soybean lectin motif (exon 9), the seven-transmembrane domain with cytoplasmic G protein coupling elements (exon 11), and three putative N-linked glycosylation sites (exon 10), consistent with preservation of significant functional domains within single exons. Exon 10 and the beginning of exon 11 along with the lectin motif are unique to the LH receptor and may be involved in specific association with the hormonal ligand. The homologous regions with other members of the glycoprotein receptor family encoded by exons 2-8, and the common amino acid motif that contains 3 conserved cysteines immediately prior to the first transmembrane region, may be involved in common hormonal interactions and in coupling functions, respectively.
促黄体生成素(LH)/人绒毛膜促性腺激素(hCG)受体基因是从大鼠肝脏基因组文库中分离出来的,从5'侧翼区的核苷酸 -2057到3'非编码末端跨度至少75千碱基对。LH受体基因编码区的结构构型由11个外显子组成,被10个内含子隔开,这些内含子都位于第一个跨膜区之前的假定细胞外结构域内。5'非编码区包含几个潜在的TATA盒和SP1启动子结合位点,以及六个回文元件、潜在的内含子/外显子剪接位点,和两个与起始密码子读框一致的延伸开放阅读框。引物延伸研究表明存在多个转录起始位点。LH/hCG受体的截短形式符合选择性剪接模式,这与完整外显子的缺失或外显子内的替代受体位点一致。所有剪接位点连接均对应于已知的供体和受体共有序列。外显子2 - 8大致对应于LH、促甲状腺激素和促卵泡激素受体cDNA中存在的14个连续20个氨基酸重复基序的区域,但每个基序有六到八个氨基酸的移位。外显子1、9、10和11不符合这种重复内含子基序。然而,这些外显子包含重要的结构元件,包括保守的半胱氨酸(外显子1、9、11)、大豆凝集素基序(外显子9)、具有细胞质G蛋白偶联元件的七跨膜结构域(外显子11),以及三个假定的N-糖基化位点(外显子10),这与单个外显子内重要功能域的保留一致。外显子10和外显子11的起始部分以及凝集素基序是LH受体特有的,可能参与与激素配体的特异性结合。由外显子2 - 8编码的与糖蛋白受体家族其他成员的同源区域,以及在第一个跨膜区之前紧邻的包含3个保守半胱氨酸的共同氨基酸基序,可能分别参与共同的激素相互作用和偶联功能。