The LIM proteins FHL1 and FHL3 are expressed differently in skeletal muscle

被引:81
作者
Morgan, MJ [1 ]
Madgwick, AJA [1 ]
机构
[1] Univ London, Eastman Dent Inst Oral Hlth Care Sci, Dept Orthodont, London WC1X 8LD, England
关键词
D O I
10.1006/bbrc.1999.0179
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have determined the complete mRNA sequence of FHL3 (formerly SLIMS). We have confirmed that it is a member of the family of LIM proteins that share a similar secondary protein structure, renamed as Four-and-a-Half-LIM domain (or FHL) proteins in accordance with this structure. The "half-LIM" domain is a single zinc finger domain that may represent a subfamily of LIM domains and defines this particular family of LIM proteins. The distribution of FHL mRNA expression within a variety of murine tissues is complex. Both FHL1 and FHL3 were expressed in a number of skeletal muscles while FHL2 was expressed at high levels in cardiac muscle. Localisation of FHL3 to human chromosome 1 placed this gene in the proximity of, but not overlapping with, alleles associated with muscle diseases. FHL1 and FHL3 mRNAs were reciprocally expressed in the murine C2C12 skeletal muscle cell line and this suggested that the pattern of expression was linked to key events in myogenesis. (C) 1999 Academic Press.
引用
收藏
页码:245 / 250
页数:6
相关论文
共 31 条
[1]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[2]   MLP-deficient mice exhibit a disruption of cardiac cytoarchitectural organization, dilated cardiomyopathy, and heart failure [J].
Arber, S ;
Hunter, JJ ;
Ross, J ;
Hongo, M ;
Sansig, G ;
Borg, J ;
Perriard, JC ;
Chien, KR ;
Caroni, P .
CELL, 1997, 88 (03) :393-403
[3]   IDENTIFICATION OF A NOVEL X-LINKED GENE RESPONSIBLE FOR EMERY-DREIFUSS MUSCULAR-DYSTROPHY [J].
BIONE, S ;
MAESTRINI, E ;
RIVELLA, S ;
MANCINI, M ;
REGIS, S ;
ROMEO, G ;
TONIOLO, D .
NATURE GENETICS, 1994, 8 (04) :323-327
[4]   Molecular cloning and characterization of FHL2, a novel LIM domain protein preferentially expressed in human heart [J].
Chan, KK ;
Tsui, SKW ;
Lee, SMY ;
Luk, SCW ;
Liew, CC ;
Fung, KP ;
Waye, MMY ;
Lee, CY .
GENE, 1998, 210 (02) :345-350
[5]  
CHEMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156
[6]   LIM domains: multiple roles as adapters and functional modifiers in protein interactions [J].
Dawid, IB ;
Breen, JJ ;
Toyama, R .
TRENDS IN GENETICS, 1998, 14 (04) :156-162
[7]   INSULIN-LIKE GROWTH FACTOR-II PRECURSOR GENE ORGANIZATION IN RELATION TO INSULIN GENE FAMILY [J].
DULL, TJ ;
GRAY, A ;
HAYFLICK, JS ;
ULLRICH, A .
NATURE, 1984, 310 (5980) :777-781
[8]  
Engle EC, 1997, AM J HUM GENET, V60, P1150
[9]   Growth hormone and the insulin-like growth factor system in myogenesis [J].
Florini, JR ;
Ewton, DZ ;
Coolican, SA .
ENDOCRINE REVIEWS, 1996, 17 (05) :481-517
[10]   Subtractive cloning and characterization of DRAL, a novel LIM-domain protein down-regulated in rhabdomyosarcoma [J].
Genini, M ;
Schwalbe, P ;
Scholl, FA ;
Remppis, A ;
Mattei, MG ;
Schafer, BW .
DNA AND CELL BIOLOGY, 1997, 16 (04) :433-442