埃迪卡拉纪镇坝微化石组合中胚胎样化石的不同步细胞分裂

IF 2.6 3区 生物学 Q2 DEVELOPMENTAL BIOLOGY
Yuan Zhang, Xingliang Zhang, Cong Liu
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引用次数: 0

摘要

埃迪卡拉类胚胎球形化石表现出不同的细胞粘附模式,类似于活体动物的部分卵裂期胚胎。从埃迪卡拉纪镇坝微化石组合中发现了两个以一对小细胞覆盖在一个大细胞上为特征的三细胞标本。它们的细胞粘附模式与翁安生物群报道的一种现象高度相似,这种现象被解释为化石胚胎正在经历盘状分裂。然而,我们的标本含有较少的细胞,因此可能代表了瓮安同类的发育前体。此外,新材料显示了几个与胚胎解释不一致的解剖学特征,包括:(1)异常大的“卵裂球”,(2)在大的“卵黄细胞”内保存着一个假定的细胞核,(3)完全分离的细胞。总的来说,真巴胚胎样标本允许重建从单细胞个体到三细胞个体的连续发育序列,这使我们将新发现的标本解释为埃迪卡拉纪胚胎样生物异常发育的产物,其亲和力尚未确定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Asynchronized cell division in embryo-like fossils from the Ediacaran Zhenba microfossil assemblage

Asynchronized cell division in embryo-like fossils from the Ediacaran Zhenba microfossil assemblage

Ediacaran embryo-like spherical fossils exhibit diverse cell adhesion patterns resembling partial cleavage-stage embryos of living animals. Two three-celled specimens characterized by a pair of small cells overlying a large cell have been recovered from the Ediacaran Zhenba microfossil assemblage. Their cell adhesion pattern is highly comparable to a phenomenon reported from the Weng'an biota that was interpreted as fossil embryos undergoing discoidal cleavage. However, our specimens contain fewer cells and thus probably represent developmental precursors of the Weng'an counterparts. Additionally, new material shows several anatomical features that are inconsistent with an embryo interpretation, including (1) an unusually large volume of “blastomeres,” (2) a putative nucleus preserved within the large “yolk cell,” and (3) completely separated cells. Collectively, the Zhenba embryo-like specimens permit a reconstruction of the consecutive developmental sequence from single-celled individuals to the three-celled individuals, leading us to interpret the newly found specimens as products of abnormal development of Ediacaran embryo-like organisms whose affinity remains unresolved.

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来源期刊
Evolution & Development
Evolution & Development 生物-发育生物学
CiteScore
6.30
自引率
3.40%
发文量
26
审稿时长
>12 weeks
期刊介绍: Evolution & Development serves as a voice for the rapidly growing research community at the interface of evolutionary and developmental biology. The exciting re-integration of these two fields, after almost a century''s separation, holds much promise as the focus of a broader synthesis of biological thought. Evolution & Development publishes works that address the evolution/development interface from a diversity of angles. The journal welcomes papers from paleontologists, population biologists, developmental biologists, and molecular biologists, but also encourages submissions from professionals in other fields where relevant research is being carried out, from mathematics to the history and philosophy of science.
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