Cyclin D1 repression of nuclear respiratory factor 1 integrates nuclear DNA synthesis and mitochondrial function.

Publication Year:
2006
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Repository URL:
http://jdc.jefferson.edu/cbfp/5
DOI:
10.1073/pnas.0603363103,
Author(s):
Wang, Chenguang; Li, Zhiping; Lu, Yinan; Du, Runlei; Katiyar, Sanjay; Yang, Jianguo; Fu, Maofu; Leader, Jennifer E; Quong, Andrew; Novikoff, Phyllis M; Pestell, Richard Show More Hide
Tags:
amino acid sequence; animals; cell cycle; cell nucleus; cultured cells; cyclin D1; DNA; hepatocytes; humans; mice; inbred; knockout; mitochondria; molecular sequence data; nuclear respiratory factor 1; recombinant fusion proteins; sequence alignment; physiology; metabolism biosynthesis; genetics; ultrastructure; phosphorylation; Amino Acids, Peptides, and Proteins
article description
Cyclin D1 promotes nuclear DNA synthesis through phosphorylation and inactivation of the pRb tumor suppressor. Herein, cyclin D1 deficiency increased mitochondrial size and activity that was rescued by cyclin D1 in a Cdk-dependent manner. Nuclear respiratory factor 1 (NRF-1), which induces nuclear-encoded mitochondrial genes, was repressed in expression and activity by cyclin D1. Cyclin D1-dependent kinase phosphorylates NRF-1 at S47. Cyclin D1 abundance thus coordinates nuclear DNA synthesis and mitochondrial function.