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Complete nucleotide sequence of mouse imunoglobulin μ gene and comparison with other immunoglobulin heavy chain genes

机译:小鼠免疫球蛋白μ基因的完整核苷酸序列,并与其他免疫球蛋白重链基因进行比较

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We have determined the complete nucleotide sequence (2168 bases) of the immunoglobulin μ gene cloned from newborn mouse DNA. The cloned l3kh fragment contained the entire constant region gene sequence that in interrupted by three intervening sequences at the junction of domains as previously shown in the γ1, γ2b and α genes. The amino acid sequence predicted by the nucleotide sequence agrees with that of the μ chain secreted by a myeloma MOPC1O4E except for 8 residues out of 448 residues. The homologous domains of the μ, γ1 and γ2b genes are more similar to each other than the different domains of the μ genes are. The result implicates that the class of the immunoglobulin heavy chain genes diverged after the heavy chain genes established the multi-domain structure. The short intervening sequences of the μ and γ genes are more conserved than the coding sequences except for the COOH-terminal domains. The results implicate that the nucleotide sequence of the intervening sequence is under selective pressure, possibly to maintain a secondary structure of the nuclear RNA to be spliced.
机译:我们已经确定了从新生小鼠DNA克隆的免疫球蛋白μ基因的完整核苷酸序列(2168个碱基)。克隆的l3kh片段包含完整的恒定区基因序列,该序列在域的交界处被三个插入序列打断,如先前在γ1,γ2b和α基因中所示。由核苷酸序列预测的氨基酸序列与骨髓瘤MOPC1O4E分泌的μ链的氨基酸序列一致,除了448个残基中的8个残基。 μ,γ1和γ2b基因的同源域比μ基因的不同域更相似。结果暗示,在重链基因建立了多结构域结构之后,免疫球蛋白重链基因的类别发生了分歧。 μ和γ基因的短插入序列比编码序列更保守,除了COOH-末端结构域。结果暗示插入序列的核苷酸序列处于选择压力下,可能维持待剪接的核RNA的二级结构。

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