Liu Z, Li P, Argue B J, Dunham R A
Department of Fisheries and Allied Aquacultures, Auburn University, Alabama 36849, USA.
Mol Mar Biol Biotechnol. 1997 Sep;6(3):217-27.
Complementary DNA (cDNA) encoding the channel catfish (Ictalurus punctatus) gonadotropin (GTH) alpha-subunit glycoprotein was cloned by polymerase chain reaction (PCR) from a plasmid library made from pituitary RNA. Complete cDNA cloning was achieved by carrying out two PCR reactions: one with an upstream sense primer plus the universal sequencing primer, located downstream of the poly(A) sequence of the cDNA in the plasmid vector, to amplify the downstream portion of the cDNA; the other with a downstream antisense primer plus the reverse-sequencing primer, located upstream of the very 5' end of the cDNA sense strand in the plasmid vector, to amplify the upstream portion of the cDNA. The two amplified fragments overlapping about 70 bp. Nucleotide sequence analysis revealed that the catfish GTH alpha-subunit was 658 bp encoding 116 amino acids and harboring a 5' nontranslated region (NTR) of 42 bp and a 3' NTR of 265 bp. The deduced amino acid sequence of the catfish GTH alpha-subunit is highly conserved with those from other cloned teleost GTH alpha-subunits. The GTH alpha-subunit was highly expressed even before induction for ovulation in females during spawning season. Administration of carp pituitary extract (a spawning-inducing reagent) induced only 1.4-fold higher expression of the GTH alpha-subunit RNA, but included very rapid egg maturation and ovulation. This unexpected result indicated that the GTH alpha-subunit may not be the limiting factor for ovulation and spawning, which may be regulated by the change of proportional coupling of the GTH alpha-subunit with specific beta-subunit during hormone-induced ovulation.
通过聚合酶链反应(PCR)从垂体RNA构建的质粒文库中克隆了编码沟鲶(Ictalurus punctatus)促性腺激素(GTH)α-亚基糖蛋白的互补DNA(cDNA)。通过进行两次PCR反应实现了完整的cDNA克隆:一次反应使用上游正义引物加上通用测序引物,该通用测序引物位于质粒载体中cDNA的聚腺苷酸(poly(A))序列下游,以扩增cDNA的下游部分;另一次反应使用下游反义引物加上反向测序引物,该反向测序引物位于质粒载体中cDNA正义链5'端的上游,以扩增cDNA的上游部分。两个扩增片段重叠约70 bp。核苷酸序列分析表明,鲶鱼GTHα-亚基为658 bp,编码116个氨基酸,具有42 bp的5'非翻译区(NTR)和265 bp的3' NTR。鲶鱼GTHα-亚基推导的氨基酸序列与其他克隆的硬骨鱼GTHα-亚基的序列高度保守。在产卵季节,雌性鲶鱼即使在诱导排卵之前,GTHα-亚基也高度表达。注射鲤鱼垂体提取物(一种产卵诱导剂)仅使GTHα-亚基RNA的表达提高了1.4倍,但却导致了非常快速的卵子成熟和排卵。这一意外结果表明,GTHα-亚基可能不是排卵和产卵的限制因素,在激素诱导排卵过程中,排卵和产卵可能受GTHα-亚基与特定β-亚基比例偶联变化的调节。