It has been proposed that C. elegans LIN-9 functions downstream of CDK4 in a pathway that regulates cell proliferation. Here, we report that mammalian BARA/LIN-9 is a predominantly nuclear protein that inhibits cell proliferation. More importantly, we demonstrate that BARA/LIN-9 also acts downstream of cyclin D/CDK4 in mammalian cells since (i) its antiproliferative effect is partially blocked by coexpression of cyclin D1, and (ii) a mutant form that lacks the first 84 amino acids rescues several phenotypic alterations observed in mice null for cdk4. Interestingly, mutation of BARA/LIN-9 restores the expression of E2F target genes in CDK4 null MEFs, indicating that the wild-type protein plays a role in the expression of genes required for the G1/S transition.
Predicate | Object |
---|---|
rdf:type | |
rdfs:comment |
It has been proposed that C. elegans LIN-9 functions downstream of CDK4 in a pathway that regulates cell proliferation. Here, we report that mammalian BARA/LIN-9 is a predominantly nuclear protein that inhibits cell proliferation. More importantly, we demonstrate that BARA/LIN-9 also acts downstream of cyclin D/CDK4 in mammalian cells since (i) its antiproliferative effect is partially blocked by coexpression of cyclin D1, and (ii) a mutant form that lacks the first 84 amino acids rescues several phenotypic alterations observed in mice null for cdk4. Interestingly, mutation of BARA/LIN-9 restores the expression of E2F target genes in CDK4 null MEFs, indicating that the wild-type protein plays a role in the expression of genes required for the G1/S transition.
|
skos:exactMatch | |
uniprot:name |
Exp. Cell Res.
|
uniprot:author |
Baida G.,
Barrett K.,
Colamonici O.R.,
Cook J.L.,
Kineman R.D.,
Kiyokawa H.,
Luque R.M.,
Pilkinton M.,
Raychaudhuri P.,
Sandoval R.,
Tian X.,
Ucker D.S.,
Valli V.E.,
Xue J.,
Zou X.
|
uniprot:date |
2006
|
uniprot:pages |
2465-2475
|
uniprot:title |
A mutant allele of BARA/LIN-9 rescues the cdk4-/- phenotype by releasing the repression on E2F-regulated genes.
|
uniprot:volume |
312
|
dc-term:identifier |
doi:10.1016/j.yexcr.2006.04.002
|