J Biol Chem 2001,
PMID: 11445556
Marignani, P A; Kanai, F; Carpenter, C L
Inactivating mutations in the serine-threonine kinase LKB1 (STK11) are found in most patients with Peutz-Jeghers syndrome; however the function of LKB1 is unknown. We found that LKB1 binds to and regulates brahma-related gene 1 (Brg1), an essential component of chromatin remodeling complexes. The association requires the N terminus of LKB1 and the helicase domain of Brg1 and LKB1 stimulates the ATPase activity of Brg1. Brg1 expression in SW13 cells induces the formation of flat cells indicative of cell cycle arrest and senescence. Expression of a kinase-dead mutant of LKB1, SL26, in SW13 cells blocks the formation of Brg1-induced flat cells, indicating that LKB1 is required for Brg1-dependent growth arrest. The inability of mutants of LKB1 to mediate Brg1-dependent growth arrest may explain the manifestations of Peutz-Jeghers syndrome.
Diseases/Pathways annotated by Medline MESH: Peutz-Jeghers Syndrome
Document information provided by NCBI PubMed
Text Mining Data
Dashed line = No text mining data
Manually curated Databases
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IRef Biogrid Interaction:
SMARCA4
—
STK11
(direct interaction, pull down)
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IRef Biogrid Interaction:
SMARCA4
—
STK11
(physical association, affinity chromatography technology)
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IRef Hprd Interaction:
SMARCA4
—
STK11
(in vivo)
-
IRef Hprd Interaction:
SMARCA4
—
STK11
(in vitro)
-
IRef Ophid Interaction:
SMARCA4
—
STK11
(aggregation, confirmational text mining)
In total, 1 gene pairs are associated to this article in curated databases