Evolution of modular and pleiotropic enhancers. Issue 2 (25th March 2022)

• Record Type: Journal Article
• Authors: Murugesan, Suriya N.; Monteiro, Antónia
• Other Names: Rebeiz Mark guestEditor.; Williams Thomas guestEditor.
• Is Part Of: Journal of experimental zoology. Volume 340:Issue 2(2023)
• Page Start: 105
• Page End: 115
• Publication Date: 2022-03-25
• Subjects: evo‐devo -- enhancers -- CREs -- evolution -- modularity -- pleiotropy; Developmental biology -- Periodicals; Evolution (Biology) -- Periodicals; Molecular evolution -- Periodicals; Zoology -- Periodicals; Evolution, Molecular -- Periodicals; Developmental Biology -- Periodicals; Zoology -- Periodicals; 591
• DOI: 10.1002/jez.b.23131
• Languages: English
• ISSNs: 1552-5007

Abstract

Abstract: 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. Abstract : We propose that most modular enhancers evolve from pleiotropic enhancers via a process of duplication followed by subfunctionalization Research Highlights: Here we discuss some of the ways (i) modular and pleiotropic Cis ‐regulatory elements (CREs) might originate; (ii) propose that many 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.