Expression of Cdk5, p35, and Cdk5-associated kinase activity in the developing rat lens

✍ Scribed by Gao, Chun Y. ;Zakeri, Zahra ;Zhu, Yong ;He, Haiying ;Zelenka, Peggy S.

• Publisher: John Wiley and Sons
• Year: 1997
• Tongue: English
• Weight: 282 KB
• Volume: 20
• Category: Article
• ISSN: 0192-253X
• DOI: 10.1002/(sici)1520-6408(1997)20:3<267::aid-dvg9>3.0.co;2-5

✦ Synopsis

We have investigated the expression of Cdk5 and its regulatory subunit, p35, in the developing rat lens from embryonic day 16 (E16) to postnatal day 8 (P8). Reverse transcription and polymerase chain reaction (RT/PCR) detected Cdk5 and p35 mRNA expression in lens epithelial cells and in differentiating lens fibers throughout this developmental period. Subsequent sequencing of the RT/PCR products confirmed their identities. In situ hybridization with Cdk5 and p35 riboprobes showed especially high expression of both mRNAs in the newly formed lens fiber cells in the bow region of the lens. Immunocytochemistry at E18 showed that Cdk5 was present in the cytoplasm of lens epithelial cells and fiber cells, with especially strong immunostaining at the anterior ends of the fibers. Fiber cells in the final stages of maturation, immediately prior to nuclear degeneration, showed positive staining for Cdk5 in the nucleus. Immunoprecipitation of proteins with Cdk5 antibody followed by immunoblotting with either N-terminal specific or C-terminal specific p35 antibodies demonstrated that p35 is complexed with Cdk5 in lens epithelial cells and lens fibers. Immunoprecipitates of Cdk5 from epithelia and fibers showed kinase activity in vitro using histone H1 as a substrate. These findings demonstrate that p35/Cdk5 activity is not restricted to neurons and raise the possibility that this kinase may play a role in lens fiber cell differentiation. Dev.