Woese Carl R
Department of Microbiology, University of Illinois at Urbana-Champaign, 601 South Goodwin Avenue, B103 Chemical and Life Sciences Laboratory, Urbana, IL 61801-3709, USA.
Proc Natl Acad Sci U S A. 2002 Jun 25;99(13):8742-7. doi: 10.1073/pnas.132266999. Epub 2002 Jun 19.
A theory for the evolution of cellular organization is presented. The model is based on the (data supported) conjecture that the dynamic of horizontal gene transfer (HGT) is primarily determined by the organization of the recipient cell. Aboriginal cell designs are taken to be simple and loosely organized enough that all cellular componentry can be altered and/or displaced through HGT, making HGT the principal driving force in early cellular evolution. Primitive cells did not carry a stable organismal genealogical trace. Primitive cellular evolution is basically communal. The high level of novelty required to evolve cell designs is a product of communal invention, of the universal HGT field, not intralineage variation. It is the community as a whole, the ecosystem, which evolves. The individual cell designs that evolved in this way are nevertheless fundamentally distinct, because the initial conditions in each case are somewhat different. As a cell design becomes more complex and interconnected a critical point is reached where a more integrated cellular organization emerges, and vertically generated novelty can and does assume greater importance. This critical point is called the "Darwinian Threshold" for the reasons given.
本文提出了一种细胞组织进化理论。该模型基于(有数据支持的)推测,即水平基因转移(HGT)的动态主要由受体细胞的组织形式决定。原始细胞设计被认为是简单且组织松散的,以至于所有细胞组成部分都可以通过HGT进行改变和/或置换,这使得HGT成为早期细胞进化的主要驱动力。原始细胞没有携带稳定的生物体谱系痕迹。原始细胞进化基本上是群体性的。进化细胞设计所需的高度新颖性是群体发明的产物,是普遍的HGT领域的产物,而非谱系内变异的产物。进化的是整个群体,即生态系统。以这种方式进化的个体细胞设计在本质上仍然是不同的,因为每种情况下的初始条件都略有不同。随着细胞设计变得更加复杂和相互关联,会达到一个临界点,此时会出现更整合的细胞组织,垂直产生的新颖性能够且确实变得更加重要。出于上述原因,这个临界点被称为“达尔文阈值”。