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Mol Cell Biol, July 1998, p. 4291-4300, Vol. 18, No. 7
Verna and Marrs McLean Department of
Biochemistry and Department of Molecular and Human Genetics, Howard
Hughes Medical Institute, Baylor College of Medicine, One Baylor Plaza,
Houston, Texas 77030
Received 23 February 1998/Returned for modification 13 April
1998/Accepted 27 April 1998
The gene coding for human cyclin K was isolated as a
CPR (cell-cycle progression restoration) gene by virtue of
its ability to impart a Far
0270-7306/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Human Cyclin K, a Novel RNA Polymerase II-Associated Cyclin
Possessing Both Carboxy-Terminal Domain Kinase and Cdk-Activating
Kinase Activity
phenotype to the budding
yeast Saccharomyces cerevisiae and to rescue the lethality
of a deletion of the G1 cyclin genes CLN1, CLN2, and CLN3. The cyclin K gene encodes a
357-amino-acid protein most closely related to human cyclins C and H,
which have been proposed to play a role in regulating basal
transcription through their association with and activation of
cyclin-dependent kinases (Cdks) that phosphorylate the
carboxyl-terminal domain (CTD) of the large subunit of RNA polymerase
II (RNAP II). Murine and Drosophila melanogaster homologs
of cyclin K have also been identified. Cyclin K mRNA is ubiquitously
expressed in adult mouse and human tissues, but is most abundant in the
developing germ cells of the adult testis and ovaries. Cyclin K is
associated with potent CTD kinase and Cdk kinase (CAK) activity in
vitro and coimmunoprecipitates with the large subunit of RNAP II. Thus,
cyclin K represents a new member of the "transcription" cyclin
family which may play a dual role in regulating Cdk and RNAP II
activity.
*
Corresponding author. Mailing address: Verna and Marrs
McLean Department of Biochemistry, Baylor College of Medicine, One Baylor Plaza, Houston, TX 77030. Phone: (713) 798-5040. Fax: (713) 798-8717. E-mail: selledge{at}bcm.tmc.edu.
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