TY - JOUR
T1 - sem-4 promotes vulval cell-fate determination in Caenorhabditis elegans through regulation of lin-39 Hox
AU - Grant, Kelly
AU - Hanna-Rose, Wendy
AU - Han, Min
N1 - Funding Information:
We thank C. Kenyon and members of her lab for lin-39 and mab-5 reagents and strains. We specifically thank Q. Ch’ng and J. Maloof for technical advice regarding lin-39 antibody staining. We thank M. Sundaram for scoring sex myoblast and coelomocyte differentiation in sem-4(ku200); M. Koelle for the sem-4<gfp construct; the C. elegans Genetic Center (University of Minnesota) for strains used in this work; D. Fay, B. Robertson, A. Spencer, and D. Starr for critically reading the manuscript; and members of the Han and Wood labs for discussions. W.H.-R. is supported by postdoctoral fellowship PF-98-113-01-DDC from the American Cancer Society. M.H. is a HHMI investigator. This work was supported by NIH Grant GM47869.
PY - 2000/8/15
Y1 - 2000/8/15
N2 - Vulval cell-fate determination in Caenorhabditis elegans requires the action of numerous gene products, including components of the Ras/Raf/MAPK signaling cascade and the hox gene lin-39. sem-4 encodes a zinc finger protein with previously characterized roles in fate specification of sex myoblasts, coelomocytes, and multiple neuronal lineages in C. elegans (M. Basson and R. Horvitz, 1996, Genes Dev. 10, 1953-1965). By characterizing three new alleles of sem-4 that we identified in a screen for vulval-defective mutants, we determined that loss of sem-4 activity results in abnormal specification of the secondary vulval cell lineages. We analyzed sem-4 interactions with other genes involved in vulval differentiation and determined that sem-4 does not function directly in the Ras-mediated signal transduction pathway but acts in close association with and upstream of lin-39 to promote vulval cell fate. We demonstrate that sem-4 regulates lin-39 expression and propose that sem-4 is a regulator of lin-39 in the vulval cell-fate determination pathway that may act to link lin-39 to incoming signals. (C) 2000 Academic Press.
AB - Vulval cell-fate determination in Caenorhabditis elegans requires the action of numerous gene products, including components of the Ras/Raf/MAPK signaling cascade and the hox gene lin-39. sem-4 encodes a zinc finger protein with previously characterized roles in fate specification of sex myoblasts, coelomocytes, and multiple neuronal lineages in C. elegans (M. Basson and R. Horvitz, 1996, Genes Dev. 10, 1953-1965). By characterizing three new alleles of sem-4 that we identified in a screen for vulval-defective mutants, we determined that loss of sem-4 activity results in abnormal specification of the secondary vulval cell lineages. We analyzed sem-4 interactions with other genes involved in vulval differentiation and determined that sem-4 does not function directly in the Ras-mediated signal transduction pathway but acts in close association with and upstream of lin-39 to promote vulval cell fate. We demonstrate that sem-4 regulates lin-39 expression and propose that sem-4 is a regulator of lin-39 in the vulval cell-fate determination pathway that may act to link lin-39 to incoming signals. (C) 2000 Academic Press.
UR - http://www.scopus.com/inward/record.url?scp=0034663073&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0034663073&partnerID=8YFLogxK
U2 - 10.1006/dbio.2000.9774
DO - 10.1006/dbio.2000.9774
M3 - Article
C2 - 10926783
AN - SCOPUS:0034663073
SN - 0012-1606
VL - 224
SP - 496
EP - 506
JO - Developmental biology
JF - Developmental biology
IS - 2
ER -