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盘基网柄菌中肌球蛋白重链缺失的发育后果。

Developmental consequences of the lack of myosin heavy chain in Dictyostelium discoideum.

作者信息

Knecht D A, Loomis W F

机构信息

Center for Molecular Genetics, University of California San Diego, La Jolla 92093.

出版信息

Dev Biol. 1988 Jul;128(1):178-84. doi: 10.1016/0012-1606(88)90280-1.

Abstract

Two different Dictyostelium discoideum cell lines that lack myosin heavy chain protein (MHC A) have been previously described. One cell line (mhcA) was created by antisense RNA inactivation of the endogenous mRNA and the other (HMM) by insertional mutagenesis of the endogenous myosin gene. The two cell lines show similar developmental defects; they are delayed in aggregation and become arrested at the mound stage. However, when cells that lack myosin heavy chain are mixed with wild-type cells, some of the mutant cells are capable of completing development to form mature spores. The pattern of expression of a number of developmentally regulated genes has been examined in both mutant cell lines. Although morphogenesis becomes aberrant before aggregation is completed, all of the markers that we have examined are expressed normally. These include genes expressed prior to aggregation as well as prespore genes expressed later in development. It appears that the signals necessary for cell-type differentiation are generated in the aborted structures formed by cells lacking MHC A. The mhcA cells have negligible amounts of MHC A protein while the HMM cells express normal amounts of a fragment of the myosin heavy chain protein similar to heavy meromyosin (HMM). The expression of myosin light chain was examined in these two cell lines. HMM cells accumulate normal amounts of the 18,000-D light chain, while the amount of light chain in mhcA cells is dramatically reduced. It is likely that the light chains assemble normally with the HMM fragment in HMM cells, while in cells lacking myosin heavy chain (mhcA) the light chains are unstable.

摘要

先前已描述了两种缺乏肌球蛋白重链蛋白(MHC A)的盘基网柄菌细胞系。一种细胞系(mhcA)是通过内源性mRNA的反义RNA失活产生的,另一种(HMM)是通过内源性肌球蛋白基因的插入诱变产生的。这两种细胞系表现出相似的发育缺陷;它们在聚集过程中延迟,并在丘状阶段停滞。然而,当缺乏肌球蛋白重链的细胞与野生型细胞混合时,一些突变细胞能够完成发育形成成熟孢子。已经在这两种突变细胞系中研究了许多发育调控基因的表达模式。尽管在聚集完成之前形态发生就变得异常,但我们检测的所有标记物都正常表达。这些标记物包括在聚集之前表达的基因以及在发育后期表达的前孢子基因。似乎细胞类型分化所需的信号是在缺乏MHC A的细胞形成的异常结构中产生的。mhcA细胞中MHC A蛋白的含量可以忽略不计,而HMM细胞表达正常量的类似于重酶解肌球蛋白(HMM)的肌球蛋白重链蛋白片段。在这两种细胞系中检测了肌球蛋白轻链的表达。HMM细胞积累正常量的18,000-D轻链,而mhcA细胞中的轻链量显著减少。很可能轻链在HMM细胞中与HMM片段正常组装,而在缺乏肌球蛋白重链的细胞(mhcA)中轻链不稳定。

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