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Human aldolase isozyme gene: the structure of multispecies aldolase B mRNAs

机译:人类醛缩酶同工酶基因:多物种醛缩酶B mRNA的结构

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A complete nucleotide sequence of human aldolase B mRNA was determined with a recombinant cDNA (pHABL120–3). The cDNA insert was composed of 1,652 bases excluding poly(A) tail and the sequence was consistent with the previous results reported by others. However, S1 nuclease mapping and subsequent genomic analysis allowed us to know that the clone possesses two more sites corresponding to 5′-termini in the 5′-noncoding region and another site of polyadenylation in the 3′-noncoding region. In fact, the major aldolase B mRNA species occupying 90% of the total mRNAs initiated at the predominant position corresponding to the position around -82 of the 5′-noncoding sequence in pHABL120–3 and terminated at the distal polyadenylation site. Second species accounting for 9% of the mRNAs initiated at the same site and terminated at the proximal polyadenylation site. The remainings have a longer 5′-noncoding sequence which starts from further upstream region of the major one and pHABL120–3 corresponds to one of these largest clones.
机译:用重组cDNA(pHABL120-3)测定了人类醛缩酶B mRNA的完整核苷酸序列。 cDNA插入片段由1,652个碱基组成,不包括poly(A)尾巴,其序列与其他人先前报道的结果一致。但是,S1核酸酶作图和随后的基因组分析使我们知道,该克隆在5'-非编码区具有两个对应于5'-末端的另外的位点,在3'-非编码区具有另一个聚腺苷酸化的位点。实际上,主要醛缩酶B mRNA占总mRNA的90%,起始于主要位置,该位置对应于pHABL120-3中5'-非编码序列的-82左右,并终止于远端聚腺苷酸化位点。占9%的mRNA的第二种物种始于同一位点,终止于近端多腺苷酸化位点。其余的具有更长的5'-非编码序列,该序列从主要序列的更上游区域开始,pHABL120-3对应于这些最大的克隆之一。

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