共查询到20条相似文献,搜索用时 31 毫秒
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Functional activity of the two promoters of the myosin alkali light chain gene in primary muscle cell cultures: comparison with other muscle gene promoters and other culture systems. 总被引:12,自引:1,他引:11
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P Daubas A Klarsfeld I Garner C Pinset R Cox M Buckingham 《Nucleic acids research》1988,16(4):1251-1271
Proximal upstream flanking sequences of the mouse myosin alkali light chain gene encoding MLC1F and MLC3F, the mouse alpha-cardiac actin gene and the chicken gene for the alpha-subunit of the acetylcholine receptor were linked to the bacterial chloramphenicol acetyl transferase (CAT) gene and transfected into primary cultures derived from mouse skeletal muscle or into myogenic cell lines. We demonstrate that the mouse MLC1F/MLC3F gene has two functional promoters. In primary muscle cultures, a 1200 bp sequence flanking exon 1 (MLC1F) and a 438 bp sequence flanking exon 2 (MLC3F) direct CAT activity in myotubes, but not in myoblasts or in non myogenic 3T6 and CV1 cells. Developmentally regulated expression is also seen with the alpha-cardiac actin (320 bp) and acetylcholine receptor alpha-subunit (850 bp) upstream sequences in the primary culture system. Transfection experiments with myogenic cell lines show different results with a given promoter construct, reflecting possible differences in the levels of regulatory factors between lines. Different muscle gene promoters behave differently in a given cell line, suggesting different regulatory factor requirements between these promoters. 相似文献
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Fast skeletal muscle myosin light chains 1 and 3 are produced from a single gene by a combined process of differential RNA transcription and splicing 总被引:50,自引:0,他引:50
M Periasamy E E Strehler L I Garfinkel R M Gubits N Ruiz-Opazo B Nadal-Ginard 《The Journal of biological chemistry》1984,259(21):13595-13604
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Robert Wade David Feldman Peter Gunning Larry Kedes 《Molecular and cellular biochemistry》1989,87(2):119-136
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The human embryonic myosin alkali light chain gene: use of alternative promoters and 3'' non-coding regions. 总被引:4,自引:2,他引:2
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M Rotter K Zimmerman A Poustka N Soussi-Yanicostas A Starzinski-Powitz 《Nucleic acids research》1991,19(7):1497-1504
Recently we have found evidence that the human embryonic myosin alkali light chain (MLC1 emb) gene has two functional promoters and that its mRNAs exhibit heterogeneity in their 3'untranslated regions (UTR). To study this more in detail we have isolated and characterized the human MLC1emb gene. We focussed in particular on 2 kilobases of 5'flanking region and the alternative 3'UTRs. RNA primer extension and S1 mapping analyses revealed that the MLC1emb gene can indeed be driven either by a proximal or a distal promoter, both in fetal and adult cardiac tissue. These MLC1emb RNAs can contain either the proximal or distal 3'UTR. In contrast to this, in fetal as well as adult masseter muscle MLC1emb mRNA is predominantly transcribed from the proximal promoter and contains mainly the distal 3'UTR. These results explain the known heterogeneity of MLC1emb mRNAs. Finally, we present evidence that the murine MLC1emb gene also contains a functional distal promoter element which has hitherto been undetected. 相似文献
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Promoter analysis of myosin alkali light chain genes expressed in mouse striated muscle. 总被引:5,自引:4,他引:1
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A Cohen P J Barton B Robert I Garner S Alonso M E Buckingham 《Nucleic acids research》1988,16(21):10037-10052
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Michael J McGrew Adrian Sherman Simon G Lillico Lorna Taylor Helen Sang 《BMC developmental biology》2010,10(1):26
Background
Regulatory elements that control expression of specific genes during development have been shown in many cases to contain functionally-conserved modules that can be transferred between species and direct gene expression in a comparable developmental pattern. An example of such a module has been identified at the rat myosin light chain (MLC) 1/3 locus, which has been well characterised in transgenic mouse studies. This locus contains two promoters encoding two alternatively spliced isoforms of alkali myosin light chain. These promoters are differentially regulated during development through the activity of two enhancer elements. The MLC3 promoter alone has been shown to confer expression of a reporter gene in skeletal and cardiac muscle in transgenic mice and the addition of the downstream MLC enhancer increased expression levels in skeletal muscle. We asked whether this regulatory module, sufficient for striated muscle gene expression in the mouse, would drive expression in similar domains in the chicken. 相似文献16.
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Y Nabeshima Y Nabeshima M Kawashima S Nakamura Y Nonomura Y Fujii-Kuriyama 《Journal of molecular biology》1988,204(3):497-505
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U Seidel E Bober B Winter S Lenz P Lohse H W Goedde K H Grzeschik H H Arnold 《Gene》1988,66(1):135-146
A set of cDNA clones coding for alkali myosin light chains (AMLC) was isolated from fetal human skeletal muscle. Nucleotide sequence analysis and RNA expression patterns of individual clones revealed related sequences corresponding to (i) fast fiber type MLC1 and MLC3; (ii) the embryonic MLC that is also expressed in fetal ventricle and adult atrium (MLCemb); and (iii) a nonsarcomeric MLC isoform that is found in all nonmuscle cell types and smooth muscle. The AMLC gene family in man comprises unique copies for MLC1, MLC3 and MLCemb, and multiple copies for the nonsarcomeric MLC genes. The gene coding for MLC1 and MLC3 is located on human chromosome 2. 相似文献