TY - JOUR
T1 - Expression patterns of FHL/SLIM family members suggest important functional roles in skeletal muscle and cardiovascular system
AU - Chu, Po Hsien
AU - Ruiz-Lozano, Pilar
AU - Zhou, Qiang
AU - Cai, Chenleng
AU - Chen, Ju
N1 - Funding Information:
We thank Dr Kenneth R. Chien for his enthusiastic support throughout the project, and Drs Sylvia Evans, Tara R. St Amand and Raymond Clark for critical reading of the manuscript. The authors would like to thank Julie Anderson and Wendy Bardwell for expert technical assistance. Dr Chu was supported by a grant from the Chung Gang Memorial Hospital at Taiwan.
PY - 2000/7/1
Y1 - 2000/7/1
N2 - LIM domain containing proteins play critical roles in animal development and cellular differentiation. Here, we describe the cloning and expression patterns of three members of the four and a half LIM domain-only protein family, FHL1, 2, and 3, from mouse. A comparison of embryonic expression patterns of these three highly-related genes indicates that they are expressed in an overlapping pattern in the developing cardiovascular system, and skeletal muscle. In adult tissues, the three genes are expressed in a predominant and overlapping manner in cardiac and skeletal muscle. Of the three genes, FHL2 appears to have the most restricted expression pattern during development, in heart, blood vessels, and skeletal muscle. Expression in heart is highest in cardiac septa and in the region adjacent to the atrio-ventricular ring, suggesting a potential role in septation or conduction system development. In the heart, FHL1expression was observed strongly in developing outflow tract, and to a lesser extent in myocardium. FHL3 displays low and ubiquitous expression during mouse development. Cardiac ventricular expression of FHL1, but not FHL2 or FHL3, was upregulated in two mouse models of cardiac hypertrophic and dilated cardiomyopathy. Taken together, these data indicate the potential importance of this FHL family in the development and maintenance of the cardiovascular system and striated muscle, and suggest that FHL1 may play a role in the development of heart disease. Copyright (C) 2000 Elsevier Science Ireland Ltd.
AB - LIM domain containing proteins play critical roles in animal development and cellular differentiation. Here, we describe the cloning and expression patterns of three members of the four and a half LIM domain-only protein family, FHL1, 2, and 3, from mouse. A comparison of embryonic expression patterns of these three highly-related genes indicates that they are expressed in an overlapping pattern in the developing cardiovascular system, and skeletal muscle. In adult tissues, the three genes are expressed in a predominant and overlapping manner in cardiac and skeletal muscle. Of the three genes, FHL2 appears to have the most restricted expression pattern during development, in heart, blood vessels, and skeletal muscle. Expression in heart is highest in cardiac septa and in the region adjacent to the atrio-ventricular ring, suggesting a potential role in septation or conduction system development. In the heart, FHL1expression was observed strongly in developing outflow tract, and to a lesser extent in myocardium. FHL3 displays low and ubiquitous expression during mouse development. Cardiac ventricular expression of FHL1, but not FHL2 or FHL3, was upregulated in two mouse models of cardiac hypertrophic and dilated cardiomyopathy. Taken together, these data indicate the potential importance of this FHL family in the development and maintenance of the cardiovascular system and striated muscle, and suggest that FHL1 may play a role in the development of heart disease. Copyright (C) 2000 Elsevier Science Ireland Ltd.
KW - Cardiac hypertrophy
KW - Cardiovasculature
KW - Four and half LIM domains
KW - MLP
KW - SLIM
KW - Skeletal muscle
UR - http://www.scopus.com/inward/record.url?scp=0034234785&partnerID=8YFLogxK
U2 - 10.1016/S0925-4773(00)00341-5
DO - 10.1016/S0925-4773(00)00341-5
M3 - Article
C2 - 10906474
AN - SCOPUS:0034234785
SN - 0925-4773
VL - 95
SP - 259
EP - 265
JO - Mechanisms of Development
JF - Mechanisms of Development
IS - 1-2
ER -