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PMID: 3683399 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Developmentally regulated expression of a truncated myosin light-chain 1F/3F gene.

Molecular and cellular biology ·Vol. 7 ·No. 10 ·1987-10-00 ·Pages 3826-9

Garfinkel LI, Davidson N

Abstract

Fast skeletal muscle myosin light-chain I (MLC1f) and myosin light-chain 3 (MLC3f) mRNAs are both derived from a single rat MLC1/3f gene. MLC1f mRNA begins at the first exon of the gene, while MLC3f mRNA begins with exon 2, 10 kilobases downstream. Both mRNAs require alternate splicing of internal exons for accurate expression. We showed that a truncated rat MLC1f/3f gene lacking exon 1 and the first 6.3 kilobases of the intron separating exons 1 and 2 produced rat MLC3f mRNA in a developmentally regulated manner after introduction into myogenic mouse cells, thus demonstrating in vivo the presence of a functional promoter associated with exon 2. Correctly spliced mRNA was produced after transfer of this truncated gene into both myogenic and nonmyogenic cells, indicating that the pattern of splicing of this complex transcript was due to a structural features of the RNA and was independent of cell type.

MeSH Terms
Animals Cell Line Gene Expression Regulation Genes Mice Myosins/genetics Promoter Regions, Genetic RNA Processing, Post-Transcriptional RNA Splicing RNA, Messenger/genetics Rats Transcription, Genetic Transfection
Chemicals
RNA, Messenger Myosins
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Garfinkel L I
Division of Chemistry, California Institute of Technology, Pasadena 91125.
Davidson N
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16 references, click to expand
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Article Info
Journal
Molecular and cellular biology
Abbr.
Mol Cell Biol
ISSN
0270-7306
Published
1987-10-00
Pages
3826-9
Language
English
Region
United States
NLM ID
8109087
PMCID
PMC368041
Subset
IM
Grants
NIGMS NIH HHS · 5F32GM09157 · United States
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