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小鼠成肌细胞及分化缺陷型变体中前列腺素内过氧化物合酶(环氧化酶)的mRNA和蛋白质生成

Prostaglandin endoperoxide synthase (cyclooxygenase) mRNA and protein production in mouse myoblasts and a differentiation-defective variant.

作者信息

Steiner S M, Keutzer J C, Hirschhorn R R

机构信息

Molecular and Cell Biology, T. H. Morgan School of Biological Sciences, University of Kentucky, Lexington 40506-0225.

出版信息

Exp Cell Res. 1991 Feb;192(2):643-6. doi: 10.1016/0014-4827(91)90088-c.

Abstract

Northern blot analysis revealed that a differentiation-defective variant (DD-1) of MM14 mouse myoblasts has seven times the prostaglandin endoperoxide synthase mRNA than the parental MM14 myoblasts. There was an even greater increase in the level of prostaglandin endoperoxide synthase protein in the DD-1 cells as compared to that in the MM14 myoblasts. In fact, prostaglandin endoperoxide synthase was not detectable by Western blot analysis of extracts from MM14 myoblasts. Since prostaglandin endoperoxide synthase has been reported to be a gene whose expression is induced transiently, i.e., growth-regulated, upon mitogen stimulation of quiescent cells, the RNA abundance of other growth-regulated genes was examined including: KC, JE, c-myc, 1B6, and vimentin. Northern blot analysis revealed that the mRNA abundance of JE, KC, and c-myc is 12-, 17-, and 2-fold higher, respectively, in growing DD-1 cells than in growing MM14 myoblasts. In contrast, there was little difference in the mRNA abundance of 1B6 and vimentin. These results are consistent with the hypothesis that increases in the levels of expression of prostaglandin endoperoxide synthase and some growth-regulated genes are integral to the expression of the differentiation-defective phenotype and may in fact contribute to this phenotype.

摘要

Northern印迹分析显示,MM14小鼠成肌细胞的一种分化缺陷变体(DD - 1)的前列腺素内过氧化物合酶mRNA含量是亲代MM14成肌细胞的7倍。与MM14成肌细胞相比,DD - 1细胞中前列腺素内过氧化物合酶蛋白水平的增加更为显著。事实上,通过对MM14成肌细胞提取物进行Western印迹分析,无法检测到前列腺素内过氧化物合酶。由于前列腺素内过氧化物合酶据报道是一个其表达在静止细胞受到有丝分裂原刺激后被短暂诱导(即生长调节)的基因,因此研究了其他生长调节基因的RNA丰度,包括:KC、JE、c - myc、1B6和波形蛋白。Northern印迹分析显示,在生长的DD - 1细胞中,JE、KC和c - myc的mRNA丰度分别比生长的MM14成肌细胞高12倍、17倍和2倍。相比之下,1B6和波形蛋白的mRNA丰度几乎没有差异。这些结果与以下假设一致,即前列腺素内过氧化物合酶和一些生长调节基因表达水平的增加是分化缺陷表型表达所必需的,并且实际上可能导致这种表型。

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