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Identification and Characterization of the CDK12/Cyclin L1 Complex Involved in Alternative Splicing Regulation†
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CORRESPONDENCE 1,10 2 3 4 5 6 Marcos Malumbres , Edward Harlow , Tim Hunt , Tony Hunter , Jill M. Lahti , Gerard Manning , 7 8 9 David O. Morgan , Li-Huei Tsai and Debra J. Wolgemuth To the Editor, tion with some cyclin-like regulatory subunit. (CrkRS) and Ched (Cdc2L5), were recently Cyclin-dependent kinases (CDKs) are protein Known family members were then renamed renamed CDK12 and CDK13, as they were kinases involved in critical cellular processes, CDK1–6, and further members (CDK7– reported to interact with cyclin L1 and cyclin such as cell cycle or transcription, whose activ- CDK10) were cloned and characterized in the L2 (refs 3, 4). ity requires association with specific cyclin sub- following years . CDK11 has been used to refer Additional members of the family, such units. Based on sequence similarity, the human to the protein encoded by three different human as PCTAIRE and PFTAIRE proteins, CCRK genome contains 21 genes encoding CDKs and loci (CDC2L1, CDC2L2 and CDC2L6) in differ- and CDC2L6, although being very similar to five additional genes encoding a more distant ent publications. CDC2L1 and CDC2L2 are two other CDKs in their primary sequence (Fig. 1) group of proteins
Nature Cell Biology – Springer Journals
Published: Nov 1, 2009
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