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A Caenorhabditis elegans TGF‐β, DBL‐1, controls the expression of LON‐1, a PR‐related protein, that regulates polyploidization and body length
Author(s) -
Morita Kiyokazu,
Flemming Anthony J.,
Sugihara Yukiko,
Mochii Makoto,
Suzuki Yo,
Yoshida Satoru,
Wood William B.,
Kohara Yuji,
Leroi Armand M.,
Ueno Naoto
Publication year - 2002
Publication title -
the embo journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.484
H-Index - 392
eISSN - 1460-2075
pISSN - 0261-4189
DOI - 10.1093/emboj/21.5.1063
Subject(s) - okazaki fragments , caenorhabditis elegans , biology , library science , genetics , computer science , gene , eukaryotic dna replication , dna repair
Using cDNA‐based array analysis combined with double‐stranded RNA interference (dsRNAi), we have identified yk298h6 as a target gene of Caenorhabditis elegans TGF‐β signaling. Worms overexpressing dbl‐1 , a TGF‐β ligand, are 16% longer than wild type. Array analysis shows yk298h6 to be one of several genes suppressed in such worms. Disruption of yk298h6 function by dsRNAi also resulted in long worms, suggesting that it is a negative regulator of body length. yk298h6 was then mapped to, and shown to be identical to, lon‐1 , a known gene that affects body length. lon‐1 encodes a 312 amino acid protein with a motif sequence that is conserved from plants to humans. Expression studies confirm that LON‐1 is repressed by DBL‐1, suggesting that LON‐1 is a novel downstream component of the C.elegans TGF‐β growth regulation pathway. Consistent with this, LON‐1 is expressed mainly in the larval and adult hypodermis and has dose‐dependent effects on body length associated with changes in hypodermal ploidy, but not hypodermal cell proliferation.