Regulation of gene expression during cell differentiation in the cellular slime molds
Regulation of gene expression during cell differentiation in the cellular slime molds
批准号:
01044080
负责人:
TAKEUCHI Ikuo
金额:
$4.1万
依托单位国家:
日本
项目类别:
Grant-in-Aid for international Scientific Research
财政年份:
1989
资助国家:
日本
项目状态:
已结题
起止时间:
1989 至 1991
中文摘要
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英文摘要
In the development of cellular slime molds, cells aggregate to form a tissue, in which two types of cells (prestalk and prespore) differentiate in the anterior and the posterior parts. To elucidate the mechanisms of cell differentiation and pattem formation, we made the following studies.(1) We have shown that cells cultured in liquid in a roller tube form an agglutinate in which prestalk, and prespore cells exhibit a definite pattern of differentiation without undergoing morphogenesis. Williams made a similar culture of cells whose expression of prestalk-specific ecmA and ecmB genes can be histochemically detected by BATA-galactosidase activity. In the agglutinates forined, cells expressing ecmA first arose randomly and then were collected to the center, while those expressing ecmB appeared on the surface layers. The result is consistent with the previous one obtained with the pattem of prespore differentiation and indicates that the differentiation pattem is tonned by sorting out of differentiated cells.(2) We have previously shown that the upstream region between -442 and -349 bp of presporespecific Dp87 gene is important for its expression. When this region is fused with the basal promoter of slime mold actin gene, the chimera gene was expressed from the vegetative stage and no difference in expression was detected between prestalk and prespore cells. This suggests that the upstream region only enhances the amount of transcription, but that cell-type-and development-specific expression is regulated by the region below -349 bp.(3) Expression of Dp87 gene during normal development was examined by using cells transformed with the promoter of Dp87 fused with BATA-galactosidase gene. Cells expressing Dp87 first appeared randomly in the aggregation streams and were later accumulated in the basal part of the aggregation centers, continuing the above notion that the differentiation pattem is formed by sorting out of differentiated cells.
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Takemoto,K.: "cAMP regulation of the expression of prespore specific genes,SP96 and Dp87 in disaggregated slug cells of Dictyostelium discoideum." Cell Differentiation and Development. 31. 89-96 (1990)
Takemoto,K.:“cAMP 对盘基网柄菌分解蛞蝓细胞中前孢子特异性基因 SP96 和 Dp87 表达的调节。”
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Tasaka,M.: "Isolation and characterization spore coat protein (Sp96) gene of Dictyostelium discoideum." Cell Differentiation and Development. 31. 1-9 (1990)
Tasaka,M.:“盘基网柄菌孢子外壳蛋白 (Sp96) 基因的分离和表征。”
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Takeuchi,I.(J.Gerhart ed.): "Cell sorting and pattern formation in Dictyostelium discoideum.In"Cell-cell interactions in early development"" Wiley-Liss,Inc, 11 (1991)
Takeuchi,I.(J.Gerhart 编辑):“盘基网柄菌中的细胞分选和模式形成。在“早期发育中的细胞-细胞相互作用”中”Wiley-Liss,Inc, 11 (1991)
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Takeuchi,I.: "Cell sorting and pattern formation in Dictyostelium discoideum.In “Cellーcell interactions in early development" (J.Gerhart ed.)" WileyーLiss,Inc, ). 02%33 (1991)
Takeuchi, I.:“盘基网柄菌中的细胞分选和模式形成。见“早期发育中的细胞-细胞相互作用”(J.Gerhart 编辑)”Wiley-Liss, Inc, 02%33 (1991)。
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Morio,T.: "Transcriptional regulation of cell-type-enriched genes during development in Dictyostelium discoideum analyzed by nuclear run-onassays." Develop.Growth &Differ.33. 293-298 (1991)
Morio,T.:“通过核运行分析分析盘基网柄菌发育过程中细胞类型富集基因的转录调控。”
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