Jameson J L, Becker C B, Lindell C M, Habener J F
Thyroid Unit, Massachusetts General Hospital, Boston.
Mol Endocrinol. 1988 Sep;2(9):806-15. doi: 10.1210/mend-2-9-806.
FSH is a pituitary gonadotropin that is encoded by separate alpha- and beta-subunit genes. We isolated a 12 kilobase (kb) DNA fragment containing the entire human FSH beta gene from a lambda phage genomic DNA library. The nucleotide sequence of the FSH beta gene predicts a 19 amino acid signal sequence and a 111 amino acid apoprotein that differs from the reported protein sequence at three residues and lacks the carboxyterminal eight amino acids, thereby bringing the human FSH beta sequence into register with those described for other mammalian species. Southern blot analyses of human genomic DNA are consistent with a single copy of the FSH beta gene per haploid genome. The FSH beta transcriptional unit spans 3.9 kb and contains two introns. The second intron (1.4 kb) is located between amino acids 35 and 36, a position that is strictly conserved among all of the glycoprotein hormone beta-subunit genes. The first intron occurs 6 base pairs upstream from the start of translation in a location analogous to that of the TSH beta gene. The first exon contains an alternate splicing donor site resulting in 5'-untranslated sequences of 63 (Exon IA) and 33 (Exon IB) bases in length. Approximately 65% of transcripts contain exon IA and 35% contain exon IB. Two different polyadenylation sites are also used. One polyadenylation site coincides with the stop codon, while the other site, which is used in greater than 80% of FSH beta mRNA transcripts, is located approximately 1 kb downstream, resulting in an unusually long 3'-untranslated sequence. The distribution of polyadenylation sites is similar for FSH beta mRNAs containing either Exons IA or IB suggesting that intron processing and polyadenylation are regulated independently. Thus, at least four distinct species of FSH beta mRNA transcripts, all encoding identical peptides, are processed from a single FSH beta gene. The distribution of different FSH beta mRNAs is similar in normal human pituitary tissue and several different FSH producing pituitary adenomas.
促卵泡激素(FSH)是一种垂体促性腺激素,由单独的α和β亚基基因编码。我们从λ噬菌体基因组DNA文库中分离出一个12千碱基(kb)的DNA片段,该片段包含整个人类FSHβ基因。FSHβ基因的核苷酸序列预测有一个19个氨基酸的信号序列和一个111个氨基酸的载脂蛋白,该载脂蛋白在三个残基处与报道的蛋白质序列不同,并且缺少羧基末端的八个氨基酸,从而使人类FSHβ序列与其他哺乳动物物种描述的序列一致。人类基因组DNA的Southern印迹分析与每个单倍体基因组中FSHβ基因的单拷贝一致。FSHβ转录单元跨度为3.9 kb,包含两个内含子。第二个内含子(1.4 kb)位于氨基酸35和36之间,该位置在所有糖蛋白激素β亚基基因中严格保守。第一个内含子出现在翻译起始点上游6个碱基对处,位置与促甲状腺激素β基因类似。第一个外显子包含一个可变剪接供体位点,导致5'非翻译序列长度分别为63个碱基(外显子IA)和33个碱基(外显子IB)。大约65%的转录本包含外显子IA,35%包含外显子IB。还使用了两个不同的聚腺苷酸化位点。一个聚腺苷酸化位点与终止密码子重合,而另一个位点(在超过80%的FSHβmRNA转录本中使用)位于下游约1 kb处,导致3'非翻译序列异常长。对于包含外显子IA或IB的FSHβmRNA,聚腺苷酸化位点的分布相似,表明内含子加工和聚腺苷酸化是独立调节的。因此,至少四种不同的FSHβmRNA转录本,均编码相同的肽,由单个FSHβ基因加工而来。不同FSHβmRNA在正常人垂体组织和几种不同的产生FSH的垂体腺瘤中的分布相似。