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[紧凑基因组]

[Compact genomes].

作者信息

Forterre P

机构信息

Institut de Génétique et Microbiologie, Centre universitaire, ORSAY, France.

出版信息

Pathol Biol (Paris). 1998 Feb;46(2):92-5.

PMID:9769917
Abstract

The number of procaryotic genomes (both Archaea and Bacteria) completely sequenced is rapidly increasing since the publication in 1995 of the first ever finished one, Haemophilis influenzae. The small size and "simplicity" of these genomes make them ideal models for training in genomic before attacking more complex genomes, but they have also great intrinsic interest. Preliminary analyses of these compact genomes have detected many orphan genes, even in organisms previously extensively studied, as well as many families of duplicated genes. A major task now is to identify the function of these orphans by a combination of in silico, biochemical and genetic analyses (examples will be presented). Several genomes of hyperthermophiles have been or will be completely sequenced soon. Many of their genes have commercial (stable proteins), as well as medical interest (crystallization of proteins with eucaryotic homologs involved in pathogenesis). However, further work with these genomes will require the development of genetic tools for these hyperthermophiles. The complete understanding of genome evolution, structure and function will require the sequencing of many genomes at the different levels of the evolutionary scale. Sequencing of genomes from closely related organisms can be relevant to study genome plasticity, whilst sequencing of genome from different domains (Archaea, Bacteria, Eucarya) can help to reconstruct the Last Universal Common Ancestor (LUCA). The latter is a difficult task and will require not only classical molecular phylogenetic studies (which can be sometimes greatly misleading) but also in depth comparative analyses of all central genetic mechanisms in the three domains to infer their respective evolution. The fundamental problem is to determine if the compact genome of procaryotes is indeed a primitive one (as suggested by the term procaryote itself) or if it has been compacted from a more complex one by evolutionary forces related to the procaryotic way of life. Finally, taking into account the extreme diversity of procaryotes and their metabolism, it should be kept in mind that beside a core of genes essential for cellular life, the myriad of procaryotic genomes contain a mine of non essential genes with potential commercial or medical application. The total number of these genes probably outnumber the total number of eucaryotic genes.

摘要

自1995年首个完成测序的原核生物基因组——流感嗜血杆菌的基因组公布以来,已完成全序列测定的原核生物基因组(古菌和细菌)数量正在迅速增加。这些基因组的小尺寸和“简单性”使其成为在研究更复杂基因组之前进行基因组学训练的理想模型,但它们本身也具有极大的研究价值。对这些紧凑基因组的初步分析发现了许多孤儿基因,即使在以前进行过广泛研究的生物体中也是如此,同时还发现了许多重复基因家族。现在的一项主要任务是通过计算机分析、生化分析和遗传分析相结合的方法来确定这些孤儿基因的功能(将举例说明)。几个嗜热菌的基因组已经或即将很快完成全序列测定。它们的许多基因具有商业价值(稳定的蛋白质)以及医学价值(与参与发病机制的真核同源物的蛋白质结晶)。然而,对这些基因组进行进一步研究将需要开发适用于这些嗜热菌的遗传工具。要全面了解基因组的进化、结构和功能,需要在进化尺度的不同层面上对许多基因组进行测序。对亲缘关系密切的生物体的基因组进行测序有助于研究基因组可塑性,而对来自不同域(古菌、细菌、真核生物)的基因组进行测序则有助于重建最后的共同祖先(LUCA)。这是一项艰巨的任务,不仅需要经典的分子系统发育研究(有时可能会产生很大的误导),还需要对这三个域中所有核心遗传机制进行深入的比较分析,以推断它们各自的进化过程。根本问题是要确定原核生物的紧凑基因组是否确实是原始的(正如原核生物这个术语本身所暗示的),或者它是否是通过与原核生物生活方式相关的进化力量从更复杂的基因组压缩而来的。最后,考虑到原核生物及其代谢的极端多样性,应该记住,除了细胞生命所必需的核心基因外,无数的原核生物基因组还包含大量具有潜在商业或医学应用价值的非必需基因。这些基因的总数可能超过真核生物基因的总数。

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