Toda S, Kajii Y, Sato M, Nishikawa T
Department of Mental Disorder Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, 4-1-1, Ogawa-Higashi, Kodaira, Tokyo, 187-8502, Japan.
Biochem Biophys Res Commun. 2000 Jul 5;273(2):723-8. doi: 10.1006/bbrc.2000.3003.
We report here the isolation and characterization of cDNA clones for a novel isoform of CDCrel-1 septin, termed CDCrel-1A, with a different 5' end sequence from the transcripts encoding the known CDCrel-1 (designated as CDCrel-1F) in the developing rat neocortex. Alternative polyadenylation site selections resulted in various transcripts for CDCrel-1A including the fusion forms with another gene, platelet glycoprotein Ibbeta (GPIbbeta). Expression of the distinct transcripts encoding CDCrel-1A and CDCrel-1F increased and decreased, respectively, from the infant to adult period. Therefore CDCrel-1A might be a major form of the CDCrel-1 septin in the adult neocortex of mammals.
我们在此报告了一种新型的CDCrel-1 九聚体异构体(称为CDCrel-1A)的cDNA克隆的分离和特性,其5'端序列与发育中的大鼠新皮质中编码已知CDCrel-1(称为CDCrel-1F)的转录本不同。可变聚腺苷酸化位点的选择导致了CDCrel-1A的各种转录本,包括与另一个基因血小板糖蛋白Ibbeta(GPIbbeta)的融合形式。从婴儿期到成年期,编码CDCrel-1A和CDCrel-1F的不同转录本的表达分别增加和减少。因此,CDCrel-1A可能是哺乳动物成年新皮质中CDCrel-1九聚体的主要形式。