Murugesan Suriya N, Monteiro Antónia
Department of Biological Sciences, National University of Singapore, Singapore.
Division of Science, Yale-NUS College, Singapore.
J Exp Zool B Mol Dev Evol. 2023 Mar;340(2):105-115. doi: 10.1002/jez.b.23131. Epub 2022 Mar 25.
Cis-regulatory elements (CREs), or enhancers, are segments of noncoding DNA that regulate the spatial and temporal expression of nearby genes. Sometimes, genes are expressed in more than one tissue, and this can be driven by two main types of CREs: tissue-specific "modular" CREs, where different CREs drive expression of the gene in the different tissues, or by "pleiotropic" CREs, where the same CRE drives expression in the different tissues. In this perspective, we will discuss some of the ways (i) modular and pleiotropic CREs might originate; (ii) propose that modular CREs might derive from pleiotropic CREs via a process of duplication, degeneration, and complementation (the CRE-DDC model); and (iii) propose that hotspot loci of evolution are associated with the origin of modular CREs belonging to any gene in a regulatory network.
顺式调控元件(CREs),即增强子,是非编码DNA片段,可调控附近基因的时空表达。有时,基因在不止一种组织中表达,这可能由两种主要类型的CREs驱动:组织特异性的“模块化”CREs,其中不同的CREs在不同组织中驱动基因表达;或“多效性”CREs,其中相同的CRE在不同组织中驱动表达。从这个角度出发,我们将讨论(i)模块化和多效性CREs可能的起源方式;(ii)提出模块化CREs可能通过复制、退化和互补过程(CRE-DDC模型)从多效性CREs衍生而来;以及(iii)提出进化热点位点与调控网络中任何基因的模块化CREs的起源相关。