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一种调节盘基网柄菌结构大小的细胞计数因子。

A cell-counting factor regulating structure size in Dictyostelium.

作者信息

Brock D A, Gomer R H

机构信息

Howard Hughes Medical Institute, Department of Biochemistry and Cell Biology MS-140, Rice University, Houston, Texas 77005-1892, USA.

出版信息

Genes Dev. 1999 Aug 1;13(15):1960-9. doi: 10.1101/gad.13.15.1960.

Abstract

Developing Dictyostelium cells form large aggregation streams that break up into groups of 0.2 x 10(5) to 1 x 10(5) cells. Each group then becomes a fruiting body. smlA cells oversecrete an unknown factor that causes aggregation streams to break up into groups of approximately 5 x 10(3) cells and thus form very small fruiting bodies. We have purified the counting factor and find that it behaves as a complex of polypeptides with an effective molecular mass of 450 kD. One of the polypeptides is a 40-kD hydrophilic protein we have named counting. In transformants with a disrupted counting gene, there is no detectable secretion of counting factor, and the aggregation streams do not break up, resulting in huge (up to 2 x 10(5) cell) fruiting bodies.

摘要

发育中的盘基网柄菌细胞形成大的聚集流,这些聚集流会分裂成每组0.2×10⁵到1×10⁵个细胞的群体。然后每个群体形成一个子实体。smlA细胞过量分泌一种未知因子,该因子会导致聚集流分裂成每组约5×10³个细胞的群体,从而形成非常小的子实体。我们已经纯化了计数因子,发现它表现为一种有效分子量为450 kD的多肽复合物。其中一种多肽是一种40-kD的亲水蛋白,我们将其命名为计数蛋白。在计数基因被破坏的转化体中,没有可检测到的计数因子分泌,聚集流也不会分裂,从而产生巨大的(多达2×10⁵个细胞)子实体。

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