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Publication : Cloning of a D-type cyclin from murine erythroleukemia cells.

First Author  Kiyokawa H Year  1992
Journal  Proc Natl Acad Sci U S A Volume  89
Issue  6 Pages  2444-7
PubMed ID  1372445 Mgi Jnum  J:2283
Mgi Id  MGI:50807 Doi  10.1073/pnas.89.6.2444
Citation  Kiyokawa H, et al. (1992) Cloning of a D-type cyclin from murine erythroleukemia cells. Proc Natl Acad Sci U S A 89(6):2444-7
abstractText  We report the complete coding sequence of a cDNA, designated CYL2, derived from a murine erythroleukemia cell library. CYL2 is considered to encode a D-type cyclin because (i) there is cross hybridization with CYL1 (a murine homolog of human cyclin D1) and the encoded protein has 64% amino acid sequence identity with CYL1 and (ii) murine erythroleukemia cell-derived CYL2 contains an amino acid sequence identical to that previously reported for the C-terminal portion of a partially sequenced CYL2. Transcripts of murine erythroleukemia cell CYL2 undergo alternative polyadenylylation like that of human cyclin D1. A major 6.5-kilobase CYL2 transcript changes its expression during the cell cycle with a broad peak through G1 and S phases and a decrease in G2/M phases. The present findings suggest that CYL2 plays a role in the G1 to S phase progression.
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