Literature DB >> 9858575

Fiber-type-specific transcription of the troponin I slow gene is regulated by multiple elements.

S Calvo1, P Venepally, J Cheng, A Buonanno.   

Abstract

The regulatory elements that restrict transcription of genes encoding contractile proteins specifically to either slow- or fast-twitch skeletal muscles are unknown. As an initial step towards understanding the mechanisms that generate muscle diversity during development, we have identified a 128-bp troponin I slow upstream element (SURE) and a 144-bp troponin I fast intronic element (FIRE) that confer fiber type specificity in transgenic mice (M. Nakayama et al., Mol. Cell. Biol. 16:2408-2417, 1996). SURE and FIRE have maintained the spatial organization of four conserved motifs (3' to 5'): an E box, an AT-rich site (A/T2) that binds MEF-2, a CACC site, and a novel CAGG motif. Troponin I slow (TnIs) constructs harboring mutations in these motifs were analyzed in transiently and stably transfected Sol8 myocytes and in transgenic mice to assess their function. Mutations of the E-box, A/T2, and CAGG motifs completely abolish transcription from the TnI SURE. In contrast, mutation of the CACC motif had no significant effect in transfected myocytes or on the slow-specific transcription of the TnI SURE in transgenic mice. To assess the role of E boxes in fiber type specificity, a chimeric enhancer was constructed in which the E box of SURE was replaced with the E box from FIRE. This TnI E box chimera, which lacks the SURE NFAT site, confers essentially the same levels of transcription in transgenic mice as those conferred by wild-type SURE and is specifically expressed in slow-twitch muscles, indicating that the E box on its own cannot determine the fiber-type-specific expression of the TnI promoter. The importance of the 5' half of SURE, which bears little homology to the TnI FIRE, in muscle-specific expression was analyzed by deletion and linker scanning analyses. Removal of the 5' half of SURE (-846 to -811) results in the loss of expression in stably transfected but not in transiently expressing myocytes. Linker scanning mutations identified sequences in this region that are necessary for the function of SURE when integrated into chromatin. One of these sites (GTTAATCCG), which is highly homologous to a bicoid consensus site, binds to nuclear proteins from several mesodermal cells. These results show that multiple elements are involved in the muscle-specific activity of the TnIs promoter and that interactions between upstream and downstream regions of SURE are important for transcription in the context of native chromatin.

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Year:  1999        PMID: 9858575      PMCID: PMC83909          DOI: 10.1128/MCB.19.1.515

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  59 in total

1.  Site-specific mutagenesis using asymmetric polymerase chain reaction and a single mutant primer.

Authors:  S Perrin; G Gilliland
Journal:  Nucleic Acids Res       Date:  1990-12-25       Impact factor: 16.971

2.  Muscle-specific expression of the troponin I gene requires interactions between helix-loop-helix muscle regulatory factors and ubiquitous transcription factors.

Authors:  H Lin; K E Yutzey; S F Konieczny
Journal:  Mol Cell Biol       Date:  1991-01       Impact factor: 4.272

3.  Transcriptional activation domain of the muscle-specific gene-regulatory protein myf5.

Authors:  T Braun; B Winter; E Bober; H H Arnold
Journal:  Nature       Date:  1990-08-16       Impact factor: 49.962

4.  A gene with homology to the myc similarity region of MyoD1 is expressed during myogenesis and is sufficient to activate the muscle differentiation program.

Authors:  D G Edmondson; E N Olson
Journal:  Genes Dev       Date:  1989-05       Impact factor: 11.361

5.  An internal regulatory element controls troponin I gene expression.

Authors:  K E Yutzey; R L Kline; S F Konieczny
Journal:  Mol Cell Biol       Date:  1989-04       Impact factor: 4.272

6.  Regulation of a segmentation stripe by overlapping activators and repressors in the Drosophila embryo.

Authors:  D Stanojevic; S Small; M Levine
Journal:  Science       Date:  1991-11-29       Impact factor: 47.728

Review 7.  The myoD gene family: nodal point during specification of the muscle cell lineage.

Authors:  H Weintraub; R Davis; S Tapscott; M Thayer; M Krause; R Benezra; T K Blackwell; D Turner; R Rupp; S Hollenberg
Journal:  Science       Date:  1991-02-15       Impact factor: 47.728

8.  Regulation of jun-B messenger RNA and AP-1 activity by light and a circadian clock.

Authors:  J M Kornhauser; D E Nelson; K E Mayo; J S Takahashi
Journal:  Science       Date:  1992-03-20       Impact factor: 47.728

9.  Structure and developmental expression of troponin I isoforms. cDNA clone analysis of avian cardiac troponin I mRNA.

Authors:  K E Hastings; R I Koppe; E Marmor; D Bader; Y Shimada; N Toyota
Journal:  J Biol Chem       Date:  1991-10-15       Impact factor: 5.157

10.  Human SRF-related proteins: DNA-binding properties and potential regulatory targets.

Authors:  R Pollock; R Treisman
Journal:  Genes Dev       Date:  1991-12       Impact factor: 11.361

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  20 in total

1.  MEF2 responds to multiple calcium-regulated signals in the control of skeletal muscle fiber type.

Authors:  H Wu; F J Naya; T A McKinsey; B Mercer; J M Shelton; E R Chin; A R Simard; R N Michel; R Bassel-Duby; E N Olson; R S Williams
Journal:  EMBO J       Date:  2000-05-02       Impact factor: 11.598

2.  A transcriptional insulator at the imprinted H19/Igf2 locus.

Authors:  C R Kaffer; M Srivastava; K Y Park; E Ives; S Hsieh; J Batlle; A Grinberg; S P Huang; K Pfeifer
Journal:  Genes Dev       Date:  2000-08-01       Impact factor: 11.361

3.  Molecular dissection of DNA sequences and factors involved in slow muscle-specific transcription.

Authors:  S Calvo; D Vullhorst; P Venepally; J Cheng; I Karavanova; A Buonanno
Journal:  Mol Cell Biol       Date:  2001-12       Impact factor: 4.272

4.  Activation of MEF2 by muscle activity is mediated through a calcineurin-dependent pathway.

Authors:  H Wu; B Rothermel; S Kanatous; P Rosenberg; F J Naya; J M Shelton; K A Hutcheson; J M DiMaio; E N Olson; R Bassel-Duby; R S Williams
Journal:  EMBO J       Date:  2001-11-15       Impact factor: 11.598

5.  Regulation of myosin heavy chain expression during rat skeletal muscle development in vitro.

Authors:  C E Torgan; M P Daniels
Journal:  Mol Biol Cell       Date:  2001-05       Impact factor: 4.138

6.  NFAT is a nerve activity sensor in skeletal muscle and controls activity-dependent myosin switching.

Authors:  Karl J A McCullagh; Elisa Calabria; Giorgia Pallafacchina; Stefano Ciciliot; Antonio L Serrano; Carla Argentini; John M Kalhovde; Terje Lømo; Stefano Schiaffino
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Review 7.  Interaction between signalling pathways involved in skeletal muscle responses to endurance exercise.

Authors:  Nathalie Koulmann; André-Xavier Bigard
Journal:  Pflugers Arch       Date:  2006-01-18       Impact factor: 3.657

8.  Activity-dependent repression of muscle genes by NFAT.

Authors:  Zaheer A Rana; Kristian Gundersen; Andres Buonanno
Journal:  Proc Natl Acad Sci U S A       Date:  2008-04-11       Impact factor: 11.205

Review 9.  Excitation-transcription coupling in skeletal muscle: the molecular pathways of exercise.

Authors:  Kristian Gundersen
Journal:  Biol Rev Camb Philos Soc       Date:  2010-10-06

10.  Evidence of MyomiR network regulation of beta-myosin heavy chain gene expression during skeletal muscle atrophy.

Authors:  John J McCarthy; Karyn A Esser; Charlotte A Peterson; Esther E Dupont-Versteegden
Journal:  Physiol Genomics       Date:  2009-08-18       Impact factor: 3.107

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