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线虫中细胞谱系的演化。

The evolution of cell lineage in nematodes.

作者信息

Sommer R J, Carta L K, Sternberg P W

机构信息

Howard Hughes Medical Institute, California Institute of Technology, Pasadena 91125, USA.

出版信息

Dev Suppl. 1994:85-95.

PMID:7579527
Abstract

The invariant development of free-living nematodes combined with the extensive knowledge of Caenorhabditis elegans developmental biology provides an experimental system for an analysis of the evolution of developmental mechanisms. We have collected a number of new nematode species from soil samples. Most are easily cultured and their development can be analyzed at the level of individual cells using techniques standard to Caenorhabditis. So far, we have focused on differences in the development of the vulva among species of the families Rhabditidae and Panagrolaimidae. Preceding vulval development, twelve Pn cells migrate into the ventral cord and divide to produce posterior daughters [Pn.p cells] whose fates vary in a position specific manner [from P1.p anterior to P12.p posterior]. In C. elegans hermaphrodites, P(3-8).p are tripotent and form an equivalence group. These cells can express either of two vulval fates (1 degree or 2 degrees) in response to a signal from the anchor cell of the somatic gonad, or a nonvulval fate (3 degrees), resulting in a 3 degrees-3 degrees-2 degrees-1 degree-2 degrees-3 degrees pattern of cell fates. Evolutionary differences in vulval development include the number of cells in the vulval equivalence group, the number of 1 degree cells, the number of progeny generated by each vulval precursor cell, and the position of VPCs before morphogenesis. Examples of three Rhabditidae genera have a posterior vulva in the position of P9-P11 ectoblasts. In Cruznema tripartitum, P(5-7).p form the vulva as in Caenorhabditis, but they migrate posteriorly before dividing. Induction occurs after the gonad grows posteriorly to the position of P(5-7).p cells. In two other species, Mesorhabditis sp. PS 1179 and Teratorhabditis palmarum, we have found changes in induction and competence with respect to their presumably more C. elegans-like ancestor. In Mesorhabditis, P(5-7).p form the vulva after migrating to a posterior position. However, the gonad is not required to specify the pattern of cell fates 3 degrees-2 degrees-1 degree-2 degrees-3 degrees. Moreover, the Pn.p cells are not equivalent in their potentials to form the vulva. A regulatory constraint in this family thus forces the same set of precursors to generate the vulva, rather than more appropriately positioned Pn.p cells.

摘要

自由生活线虫的不变发育,结合对线虫发育生物学的广泛了解,为分析发育机制的进化提供了一个实验系统。我们从土壤样本中收集了许多新的线虫物种。大多数物种易于培养,并且可以使用线虫标准技术在单个细胞水平上分析它们的发育。到目前为止,我们专注于小杆线虫科和类圆线虫科物种外阴发育的差异。在外阴发育之前,十二个Pn细胞迁移到腹索并分裂产生后代[Pn.p细胞],其命运以位置特异性方式变化[从P1.p前部到P12.p后部]。在线虫雌雄同体中,P(3 - 8).p是三能干细胞并形成一个等价组。这些细胞可以响应来自体细胞性腺锚定细胞的信号,表达两种外阴命运之一(1度或2度),或者非外阴命运(3度),从而产生3度 - 3度 - 2度 - 1度 - 2度 - 3度的细胞命运模式。外阴发育的进化差异包括外阴等价组中的细胞数量、1度细胞的数量、每个外阴前体细胞产生的后代数量,以及形态发生前VPCs的位置。三个小杆线虫科属的例子在P9 - P11外胚层细胞的位置有后外阴。在三叉克鲁兹线虫中,P(5 - 7).p像在线虫中一样形成外阴,但它们在分裂前向后迁移。诱导发生在性腺向后生长到P(5 - 7).p细胞位置之后。在另外两个物种中,中杆线虫属PS 1179和掌状畸线线虫,我们发现相对于它们可能更像线虫的祖先,诱导和感受态发生了变化。在中杆线虫中,P(5 - 7).p迁移到后部位置后形成外阴。然而,指定3度 - 2度 - 1度 - 2度 - 3度的细胞命运模式不需要性腺。此外,Pn.p细胞形成外阴的潜力并不等同。因此,这个家族中的一种调节限制迫使同一组前体细胞产生外阴,而不是更合适定位的Pn.p细胞。

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