Yanagisawa S, Izui K, Yamaguchi Y, Shigesada K, Katsuki H
Department of Chemistry, Faculty of Science, Kyoto University, Japan.
FEBS Lett. 1988 Feb 29;229(1):107-10. doi: 10.1016/0014-5793(88)80807-x.
Four clones of cDNA for phosphoenolpyruvate carboxylase [EC 4.1.1.31] were obtained from a maize green leaf cDNA library by colony hybridization. The largest cDNA was of full-length (3335 nucleotides), being 243 nucleotides longer than the cDNA cloned previously [(1986) Nucleic Acids Res. 14, 1615-1628]. Alignment of the sequence for the N-terminal coding region found in two of the four clones with the sequence reported previously, established the sequence of the entire coding region for the enzyme. The sequencing of 3'-untranslated region of the clones revealed that the poly(A) tract is attached at multiple sites in vivo.
通过菌落杂交从玉米绿叶cDNA文库中获得了4个磷酸烯醇式丙酮酸羧化酶[EC 4.1.1.31]的cDNA克隆。最大的cDNA是全长的(3335个核苷酸),比先前克隆的cDNA长243个核苷酸[(1986年)《核酸研究》14卷,1615 - 1628页]。将4个克隆中的2个克隆中发现的N端编码区序列与先前报道的序列进行比对,确定了该酶整个编码区的序列。对这些克隆的3'非翻译区进行测序表明,在体内多聚腺苷酸尾附着于多个位点。