REPROGRAMMING OF MYOSIN LIGHT CHAIN 1/3 EXPRESSION IN MUSCLE HETEROKARYONS

被引:11
|
作者
PAJAK, L [1 ]
MARIAPPAN, M [1 ]
WIECZOREK, DF [1 ]
机构
[1] UNIV CINCINNATI,COLL MED,DEPT MOLEC GENET BIOCHEM & MICROBIOL,CINCINNATI,OH 45267
关键词
D O I
10.1016/0012-1606(91)90210-T
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Fast myosin light chain (MLC) 1 3 is one of the few genes which regulates transcript production at both transcriptional and post-transcriptional levels, utilizing two functionally distinct promoters coupled with alternatively spliced exons. The transcriptional process controlling expression from this single gene locus is developmentally regulated, such that MLC 1 precedes MLC 3 during myogenesis. Results from our RNA analyses demonstrate that in differentiated rat L6E9 muscle, MLC 3 is the sole isoform expressed from the MLC 1 3 locus. However, we also show that by generating rat L6E9:mouse C2 muscle heterokaryons, MLC 1 expression from the L6E9 MLC locus can be induced. In addition to novel rat MLC 1 expression in the C2:L6E9 heterokaryons, we show that the synthesis profile of rat MLC 3 mRNA is also altered relative to L6E9 muscle cultured alone. Additional experiments demonstrate that the reprogramming of rat MLC 1 and 3 expression in the muscle heterokaryons requires that C2 and L6E9 nuclei be contained within a common cytoplasm. These results demonstrate that expression from the MLC 1 3 gene is "plastic," and is not under the control of a strict developmental program but, rather, can be modified by the environmental milieu. © 1991.
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页码:28 / 39
页数:12
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