Kondo T, Furuta T, Mitsunaga K, Ebersole T A, Shichiri M, Wu J, Artzt K, Yamamura K, Abe K
Institute of Molecular Embryology and Genetics, Kumamoto University School of Medicine, 4-24-1 Kuhonji, Kumamoto 862-0976, Japan.
Mamm Genome. 1999 Jul;10(7):662-9. doi: 10.1007/s003359901068.
qkI, encoding a KH domain-containing RNA binding protein, has been isolated as a candidate gene for the mouse neurological mutation quaking. Here, we describe detailed studies on its genomic structure and expression pattern. We isolated approximately 1 Mb of genomic region containing the quaking locus and determined its genomic organization. The qkI locus contains at least 9 exons spanning approximately 65 kb of DNA. It gives rise to six distinct transcripts encoding, theoretically, five different protein isoforms. Exons 1 through 4 are shared by all the transcripts, whereas coding exons and two distinct 3'-UTRs downstream to the exon 4 are differentially utilized. One isoform has a truncated KH domain and may act as an antagonist to the others. These findings and identification of a single transcription initiation site suggest that differential expression of each transcript is regulated by alternative splicing. Expression of each alternative transcript and protein product was also examined. Two types of transcripts, 5 kb-A and B, are most abundant in the brain of newborn mice and are gradually downregulated thereafter. In contrast, the other three messages, 6 kb, 7 kb-A and B, increase as myelination proceeds and peak at 2 weeks of age, corresponding to the most active stage of myelination. Although the qkI messages and their products are abundant in brain and heart, a lower level of expression was found in various other tissues tested. Alternative transcripts that share the same 3'-UTR showed very similar expression patterns, suggesting a regulatory role of the 3'-UTRs in qkI gene expression.
qkI编码一种含KH结构域的RNA结合蛋白,已被分离出来作为小鼠神经学突变颤抖(quaking)的候选基因。在此,我们描述了对其基因组结构和表达模式的详细研究。我们分离出了包含颤抖基因座的约1兆碱基的基因组区域,并确定了其基因组组织。qkI基因座包含至少9个外显子,跨越约65千碱基的DNA。它产生六种不同的转录本,理论上编码五种不同的蛋白质异构体。所有转录本都共享外显子1至4,而编码外显子和外显子4下游的两个不同的3'非翻译区(3'-UTR)则被差异利用。一种异构体具有截短的KH结构域,可能对其他异构体起拮抗作用。这些发现以及单个转录起始位点的鉴定表明,每个转录本的差异表达受可变剪接调控。我们还检测了每个可变转录本和蛋白质产物的表达。两种类型的转录本,5 kb-A和B,在新生小鼠大脑中最为丰富,此后逐渐下调。相比之下,其他三种转录本,6 kb、7 kb-A和B,随着髓鞘形成的进行而增加,并在2周龄时达到峰值,这与髓鞘形成最活跃的阶段相对应。尽管qkI转录本及其产物在脑和心脏中丰富,但在测试的其他各种组织中发现表达水平较低。共享相同3'-UTR的可变转录本显示出非常相似的表达模式,表明3'-UTR在qkI基因表达中具有调控作用。