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在球形Acytostelium 亚群的子实体形成过程中的时间和非永久性分工。

Temporal and non-permanent division of labor during sorocarp formation in the social amoeba Acytostelium subglobosum.

机构信息

Faculty of Life and Environmental Sciences, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki 305-8572, Japan.

出版信息

Dev Biol. 2013 Mar 15;375(2):202-9. doi: 10.1016/j.ydbio.2013.01.003. Epub 2013 Jan 8.

Abstract

Somatic cell differentiation is crucial for the development of multicellular organisms. While the development of a fruiting body in Dictyostelium discoideum represents a simple model of this process with separation of stalk cells from the spore lineage, that of Acytostelium subglobosum is not accompanied by cell type separation. This species produces acellular stalks and, seemingly, all aggregated amoebae become spores; however, it possesses homologs for the stalk-cell marker genes of D. discoideum. In this study, we analyzed the spatio-temporal expression of A. subglobosum orthologs for D. discoideum stalk- or spore-lineage markers to clarify the developmental process of A. subglobosum. We first found that the prespore vesicles, which contained spore coat proteins, started to accumulate in the tip region and were observed in the entire sorogen throughout later development, confirming that all A. subglobosum cells became spores. The expression of a stalk-lineage gene ortholog, As-ecmA, started at the mound stage and was prominent in the protruding sorogen. Although two spore-lineage gene orthologs, As-cotD1 and -cotD2, were likewise detected shortly after cell aggregation and increased in intensity until tip formation, their expression diminished in the protruding sorogen. Double-fluorescence staining of these prestalk and prespore marker genes revealed that the expression of these marker genes was mutually exclusive and that expression switching occurred in the early tip. Our results indicate that A. subglobosum cells become committed to the spore lineage first, and then, while keeping this commitment intact, participate in stalk formation. Instead of the permanent division of labor observed in D. discoideum, A. subglobosum produces fruiting bodies by all cells contributing to the formation of the stalk as well as forming spores.

摘要

体细胞分化对于多细胞生物的发育至关重要。虽然盘基网柄菌(Dictyostelium discoideum)的子实体发育代表了一个简单的过程模型,其中柄细胞与孢子谱系分离,但粘菌(Acytostelium subglobosum)的发育过程则没有伴随细胞类型的分离。该物种产生无细胞的柄,而且所有聚集的变形虫似乎都成为孢子;然而,它拥有与盘基网柄菌的柄细胞标记基因的同源物。在这项研究中,我们分析了粘菌中盘基网柄菌的柄细胞或孢子谱系标记基因的时空表达,以阐明粘菌的发育过程。我们首先发现,含有孢子外壳蛋白的前孢子泡开始在尖端区域积累,并在整个索原体中观察到,这证实了所有粘菌细胞都成为了孢子。一个柄细胞谱系基因的同源物,As-ecmA 的表达始于丘状体阶段,并在突出的索原体中表现突出。尽管两个孢子谱系基因的同源物,As-cotD1 和 -cotD2,也在细胞聚集后不久被检测到,并在尖端形成之前增加强度,但它们在突出的索原体中的表达减少。这些前柄和前孢子标记基因的双荧光染色表明,这些标记基因的表达是相互排斥的,并且表达转换发生在早期的尖端。我们的结果表明,粘菌细胞首先成为孢子谱系的决定细胞,然后在保持这种决定的同时,参与柄的形成。与盘基网柄菌中观察到的永久分工不同,粘菌通过所有细胞参与柄的形成以及形成孢子来产生子实体。

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