de Lorenzo Víctor
Systems & Synthetic Biology Program, Centro Nacional de Biotecnología CSIC Cantoblanco, Madrid, Spain.
Bioessays. 2014 Mar;36(3):226-35. doi: 10.1002/bies.201300153. Epub 2014 Jan 14.
The standard representation of the Central Dogma (CD) of Molecular Biology conspicuously ignores metabolism. However, both the metabolites and the biochemical fluxes behind any biological phenomenon are encrypted in the DNA sequence. Metabolism constrains and even changes the information flow when the DNA-encoded instructions conflict with the homeostasis of the biochemical network. Inspection of adaptive virulence programs and emergence of xenobiotic-biodegradation pathways in environmental bacteria suggest that their main evolutionary drive is the expansion of their metabolic networks towards new chemical landscapes rather than perpetuation and spreading of their DNA sequences. Faulty enzymatic reactions on suboptimal substrates often produce reactive oxygen species (ROS), a process that fosters DNA diversification and ultimately couples catabolism of the new chemicals to growth. All this calls for a revision of the CD in which metabolism (rather than DNA) has the leading role.
分子生物学中心法则(CD)的标准表述明显忽略了新陈代谢。然而,任何生物现象背后的代谢物和生化通量都被编码在DNA序列中。当DNA编码的指令与生化网络的稳态发生冲突时,新陈代谢会限制甚至改变信息流。对环境细菌中适应性毒力程序和异源生物降解途径出现的研究表明,它们主要的进化驱动力是其代谢网络向新的化学领域扩展,而非其DNA序列的延续和传播。在次优底物上发生的错误酶促反应通常会产生活性氧(ROS),这一过程促进了DNA多样化,并最终将新化学物质的分解代谢与生长联系起来。所有这些都要求对中心法则进行修订,其中新陈代谢(而非DNA)应起主导作用。