Müller D, Rehbein M, Baumeister H, Richter D
Institut für Zellbiochemie, UKE, Universität Hamburg, Germany.
Nucleic Acids Res. 1992 Apr 11;20(7):1471-5. doi: 10.1093/nar/20.7.1471.
A cDNA has been isolated from a rat testis library which encodes a novel protein of 100 kDa that contains domains found in two different proteins involved in the processing of pre-mRNAs. Computer-assisted comparison reveals that one sequence motif of 30 amino-acid residues is very similar to a region conserved in the C-terminal part of eukaryotic poly(A) binding proteins (PABP). A second region of the rat 100 kDa protein, containing alternating basic, mostly arginine, and acidic amino-acid residues, is structurally related to sequence motifs found in the 70K protein of the U1 small nuclear ribonucleoprotein particle (snRNP), which is involved in RNA splicing. Northern blot analysis shows that a corresponding 9.5 kb transcript is highly expressed in rat testis; lower mRNA levels are found in other tissues such as liver, kidney, lung and brain. Ontogenic studies reveal that the expression of the 100 kDa protein-encoding gene and sexual maturation are correlated, being barely detectable during early post-natal life but reaching maximal levels around the first month after birth.
已从大鼠睾丸文库中分离出一种互补DNA(cDNA),它编码一种100千道尔顿的新型蛋白质,该蛋白质含有在参与前体信使核糖核酸(pre-mRNA)加工的两种不同蛋白质中发现的结构域。计算机辅助比较显示,一个由30个氨基酸残基组成的序列基序与真核多聚腺苷酸结合蛋白(PABP)C端保守区域非常相似。大鼠100千道尔顿蛋白质的第二个区域包含交替的碱性氨基酸(主要是精氨酸)和酸性氨基酸残基,在结构上与U1小核核糖核蛋白颗粒(snRNP)的70K蛋白质中发现的序列基序相关,U1 snRNP参与RNA剪接。Northern印迹分析表明,相应的9.5千碱基转录本在大鼠睾丸中高度表达;在肝脏、肾脏、肺和脑等其他组织中发现较低的信使核糖核酸(mRNA)水平。个体发育研究表明,编码100千道尔顿蛋白质的基因表达与性成熟相关,在出生后早期几乎检测不到,但在出生后第一个月左右达到最高水平。