Evolution of complexity in signaling pathways

被引:62
作者
Soyer, Orkun S. [1 ]
Bonhoeffer, Sebastian [1 ]
机构
[1] ETH, Swiss Fed Inst Technol, Theoret Biol Grp, Inst Integrat Biol,ETH Zentrum, CH-8092 Zurich, Switzerland
关键词
robustness; evolutionary simulations; mathematical models; protein pathways; signal transduction;
D O I
10.1073/pnas.0604449103
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
It is not clear how biological pathways evolve to mediate a certain physiological response and why they show a level of complexity that is generally above the minimum required to achieve such a response. One possibility is that pathway complexity increases due to the nature of evolutionary mechanisms. Here, we analyze this possibility by using mathematical models of biological pathways and evolutionary simulations. Starting with a population of small pathways of three proteins, we let the population evolve with mutations that affect pathway structure through duplication or deletion of existing proteins, deletion or creation of interactions among them, or addition of new proteins. Our simulations show that such mutational events, coupled with a selective pressure, leads to growth of pathways. These results indicate that pathways could be driven toward complexity via simple evolutionary mechanisms and that complexity can arise without any specific selective pressure for it. Furthermore, we find that the level of complexity that pathways evolve toward depends on the selection criteria. In general, we find that final pathway size tends to be lower when pathways evolve under stringent selection criteria. This leads to the counterintuitive conclusion that simple response requirements on a pathway would facilitate its evolution toward higher complexity.
引用
收藏
页码:16337 / 16342
页数:6
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