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Sequences of liver cDNAs encoding two different mouse insulin-like growth factor I precursors

机译:编码两种不同小鼠胰岛素样生长因子I前体的肝CDNA序列

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Complementary DNAs encoding mouse liver insulin-like growth factor I (IGF-I) have been isolated and sequenced. Alternative RNA splicing results in the synthesis of two types of mouse IGF-I precursor that differ in the size and sequence of the COOH-tenninal peptide. The sequences of the signal peptides, IGF-I moieties and the first 16 amino acids of the COOH-terminal peptides or E-domains of the two precursors are identical. The sequence difference results from the presence in preproIGF-IB mRNA of a 52 base insertion which introduces a 17 amino acid segment into the COOH-terminal peptide of preproIGF-IB and also causes a shift in the reading frame of the mRNA. As a consequence of this insertion, the COOH-terminal 19 and 25 amino acids of mouse preproIGF-IA and -IB, respectively, are different. The sequences of mouse and human preproIGF-IA are highly conserved and possess 94Z identity. In contrast, the sequences of mouse and human preproIGF-IB are quite different in the region of the COOH-terminal peptide. A comparison of the sequences of mouse and human preproIGF-IB mRNA indicates that they are generated by different molecular mechanisms.
机译:编码小鼠肝胰岛素样生长因子I(IGF-1)的互补DNA已被分离和测序。替代的RNA剪接导致两种类型的小鼠IGF-1前体的合成,其尺寸和官能曲线肽的尺寸和序列不同。信号肽的序列,IGF-I部分和两种前体的CoOH-末端肽的第一16个氨基酸或两种前体的E-域的序列相同。序列差异由52碱基插入的前预浸族-IB mRNA中的存在,其将17个氨基酸区段引入预浸植物预口-1b的核 - 末端肽中,并且还导致mRNA的读取框架的偏移。作为这种插入的结果,COOH-末端19和25分别是小鼠PROGROIGF-IA和-IB的氨基酸不同。小鼠和人类前素序列高度保守并拥有94Z身份。相反,小鼠和人前蛋白酶序列在CoOH-末端肽的区域中是完全不同的。小鼠和人前序列序列的比较表明它们是由不同的分子机制产生的。

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