Suppr超能文献

巨型系统发育、细胞体模式、适应带:真核生物基部辐射的原因和时间

Megaphylogeny, cell body plans, adaptive zones: causes and timing of eukaryote basal radiations.

作者信息

Cavalier-Smith Thomas

机构信息

Department of Zoology, University of Oxford, South Parks Road, Oxford OX1 3PS, United Kingdom.

出版信息

J Eukaryot Microbiol. 2009 Jan-Feb;56(1):26-33. doi: 10.1111/j.1550-7408.2008.00373.x.

Abstract

I discuss eukaryote megaphylogeny and the timing of major innovations in the light of multigene trees and the rarity of marine/freshwater evolutionary transitions. The first eukaryotes were aerobic phagotrophs, probably substratum-associated heterotrophic amoeboflagellates. The primary eukaryote bifurcation generated unikonts (ancestrally probably unicentriolar, with a conical microtubular [MT] cytoskeleton) and bikonts (ciliary transformation from anterior cilium to ancestrally gliding posterior cilium; cytoskeleton of ventral MT bands). Unikonts diverged into Amoebozoa with anterior cilia, lost when lobosan broad pseudopods evolved for locomotion, and Choanozoa with posterior cilium and filose pseudopods that became unbranched tentacles/microvilli in holozoa and eventually the choanoflagellate/choanocyte collar. Of choanozoan ancestry, animals evolved epithelia, fibroblasts, eggs, and sperm. Fungi and Ichthyosporea evolved walls. Bikonts, ancestrally with ventral grooves, include three adaptively divergent megagroups: Rhizaria (Retaria and Cercozoa, ancestrally reticulofilose soft-surfaced gliding amoeboflagellates), and the originally planktonic Excavata, and the corticates (Plantae and chromalveolates) that suppressed pseudopodia. Excavata evolved cilia-generated feeding currents for grooval ingestion; corticates evolved cortical alveoli and ciliary hairs. Symbiogenetic origin and transfers of chloroplasts stimulated an explosive radiation of corticates--hard to resolve on multigene trees--and opisthokonts, and ensuing Cambrian explosions of animals and protists. Plantae lost phagotrophy and multiply evolved walls and macroalgae. Apusozoa, with dorsal pellicle and ventral pseudopods, are probably the most divergent bikonts or related to opisthokonts. Eukaryotes probably originated 800-850 My ago. Amoebozoa, Apusozoa, Loukozoa, and Metamonada may be the only extant eukaryote phyla pre-dating Neoproterozoic snowball earth. New subphyla are established for Choanozoa and Loukozoa; Amoebozoa are divided into three revised subphyla, with Variosea transferred into Conosa.

摘要

我根据多基因树以及海洋/淡水进化转变的罕见性,讨论了真核生物的宏观系统发育和主要创新的时间。最早的真核生物是需氧吞噬生物,可能是与基质相关的异养变形鞭毛虫。真核生物的第一次分支产生了单鞭毛生物(最初可能是单中心粒的,具有锥形微管[MT]细胞骨架)和双鞭毛生物(从前端纤毛到最初用于滑行的后端纤毛的纤毛转变;腹侧MT带的细胞骨架)。单鞭毛生物分化为具有前端纤毛的变形虫门,当叶状宽伪足进化用于运动时前端纤毛消失,以及具有后端纤毛和丝状伪足的领鞭毛虫门,丝状伪足在全动物中变成无分支的触手/微绒毛,最终成为领鞭毛虫/领细胞环。在领鞭毛虫门的祖先中,动物进化出上皮、成纤维细胞、卵子和精子。真菌和鱼孢菌进化出细胞壁。双鞭毛生物最初具有腹侧凹槽,包括三个适应性分化的大类群:根足亚纲(放射虫纲和丝足虫纲,最初是网状丝状软表面滑行变形鞭毛虫)、最初浮游的挖掘类群,以及抑制伪足的皮层类群(植物界和色藻界)。挖掘类群进化出由纤毛产生的摄食流用于凹槽摄食;皮层类群进化出皮层小泡和纤毛。叶绿体的共生起源和转移刺激了皮层类群和后鞭毛生物的爆发性辐射——在多基因树上难以解析——以及随后动物和原生生物的寒武纪爆发。植物界失去了吞噬营养,多次进化出细胞壁和大型藻类。无尾目生物具有背侧表膜和腹侧伪足,可能是最具分歧的双鞭毛生物或与后鞭毛生物相关。真核生物可能起源于8亿至8.5亿年前。变形虫门、无尾目生物、裸口亚纲和单鞭毛生物可能是仅有的现存早于新元古代雪球地球的真核生物门类。为领鞭毛虫门和裸口亚纲建立了新的亚门;变形虫门分为三个修订后的亚门,并将多变亚纲转移到锥虫亚纲。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验