TY - JOUR
T1 - Pw1, a novel zinc finger gene implicated in the myogenic and neuronal lineages
AU - Relaix, Frédéric
AU - Weng, Xun
AU - Marazzi, Giovanna
AU - Yang, Ellen
AU - Copeland, Neal
AU - Jenkins, Nancy
AU - Spence, Sally E.
AU - Sassoon, David
N1 - Funding Information:
We acknowledge P. Chambon and T. Lufkin for the 11-day p.c. mouse cDNA library. We thank Debra J. Gilbert for excellent technical assistance. In addition we thank Karl Dengenhardt and Cary Miller for helpful comments on the manuscript. This research was supported, in part, by the National Cancer Institute, DHHS, under contract with ABL to N.J. and N.C. and a Hirschl Fellowship and the Council for Tobacco Research to D.S.
PY - 1996/8/1
Y1 - 1996/8/1
N2 - The cellular and molecular processes leading to the establishment of the skeletal muscle lineage in the vertebrate are not well understood. The MyoD-related family of myogenic regulatory factors (MRFs) are expressed during somitogenesis although cells with myogenic capacity are present prior to gastrulation. We propose that regulatory genes exist that guide the skeletal muscle lineage during early development. In an effort to identify these regulatory genes, we performed a differential screening to isolate transcripts that are present in myogenic cells and in the embryo prior to MRF expression but absent in nonmyogenic fibroblasts. We report here the identification of Pw1. The Pw1 transcript is ~ 8.5 kb long and encodes a large protein containing 12 widespread C2H2 zinc fingers and 3 motifs containing periodic prolines and acidic residues. Consistent with the possibility that Pw1 is a transcription factor, we observe nuclear localization of the protein. Pw1 is strongly expressed upon gastrulation and subsequently becomes restricted to skeletal muscle and subregions of the central nervous system. Pw1 is initially expressed in all mesodermal cells early in development; however, its maintained expression in adult differentiated muscle suggests a specific role in the skeletal muscle lineage. Pw1 expression is cell cycle specific with levels highest during late M-phase. The gene is intronless which may facilitate transcription during cell division. At present, the precise function of Pw1 is not understood; however, we note that Pw1 maps to the proximal region of chromosome 7 near the axial segmentation mutant pudgy which shows severe perturbation of axial skeletal and muscle structures.
AB - The cellular and molecular processes leading to the establishment of the skeletal muscle lineage in the vertebrate are not well understood. The MyoD-related family of myogenic regulatory factors (MRFs) are expressed during somitogenesis although cells with myogenic capacity are present prior to gastrulation. We propose that regulatory genes exist that guide the skeletal muscle lineage during early development. In an effort to identify these regulatory genes, we performed a differential screening to isolate transcripts that are present in myogenic cells and in the embryo prior to MRF expression but absent in nonmyogenic fibroblasts. We report here the identification of Pw1. The Pw1 transcript is ~ 8.5 kb long and encodes a large protein containing 12 widespread C2H2 zinc fingers and 3 motifs containing periodic prolines and acidic residues. Consistent with the possibility that Pw1 is a transcription factor, we observe nuclear localization of the protein. Pw1 is strongly expressed upon gastrulation and subsequently becomes restricted to skeletal muscle and subregions of the central nervous system. Pw1 is initially expressed in all mesodermal cells early in development; however, its maintained expression in adult differentiated muscle suggests a specific role in the skeletal muscle lineage. Pw1 expression is cell cycle specific with levels highest during late M-phase. The gene is intronless which may facilitate transcription during cell division. At present, the precise function of Pw1 is not understood; however, we note that Pw1 maps to the proximal region of chromosome 7 near the axial segmentation mutant pudgy which shows severe perturbation of axial skeletal and muscle structures.
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U2 - 10.1006/dbio.1996.0172
DO - 10.1006/dbio.1996.0172
M3 - Article
C2 - 8806818
AN - SCOPUS:0030220274
SN - 0012-1606
VL - 177
SP - 383
EP - 396
JO - Developmental Biology
JF - Developmental Biology
IS - 2
ER -