| FEBS Letters | |
| Premature termination of transcription and alternative splicing in the human transacylase (E2) gene of the branched‐chain α‐ketoacid dehydrogenase complex | |
| Lee, Jun2  Chuang, David T.2  Cox, Rody P.1  Fisher, Charles W.2  Lau, Kim S.2  | |
| [1] Department of Internal Medicine, The University of Texas Southwestern Medical Center, Dallas, TX 75235-9038, USA;Department of Biochemistry, The University of Texas Southwestern Medical Center, Dallas, TX 75235-9038, USA | |
| 关键词: Genomic clone; cDNA; E2 gene; Alternative splicing; | |
| DOI : 10.1016/0014-5793(91)80155-V | |
| 学科分类:生物化学/生物物理 | |
| 来源: John Wiley & Sons Ltd. | |
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【 摘 要 】
We have isolated a human genomic clone hgE2-14 containing exons 5,6,7 and 8 of the branched-chain α-ketoacid dehydrogenase E2 transacylase gene. Sequencing of exon B and its surrounding intronic sequences reveals complete identity with the previously reported truncated E2 cDNA (hE2-1) sequence between nucleotides 938 and 1521. We have identified consensus splice site junctions flanking exon 8 and also a cryptic 3??? splice site 370 bases upstream from the start of exon 8 in the gene. In addition, two polyadenylation signals located in the hE2-1 cDNA are also present in the intronic sequence downstream of exon 8 which promote termination of transcription. The data indicate that shortened human liver E2 transcripts undergo alternative splicing to yield mRNA of the hE2-1 type.
【 授权许可】
Unknown
【 预 览 】
| Files | Size | Format | View |
|---|---|---|---|
| RO201912020294517ZK.pdf | 274KB |
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