TY - JOUR
T1 - Transposable Element Mediated Innovation in Gene Regulatory Landscapes of Cells
T2 - Re-Visiting the “Gene-Battery” Model
AU - Sundaram, Vasavi
AU - Wang, Ting
N1 - Funding Information:
V.S. was supported by a fellowship from the EMBL Interdisciplinary Postdoc (EIPOD) programme under Marie Skłodowska-Curie actions COFUND (grant number 664726). T.W. was supported by NIH grants 5R01HG007354, 5R01HG007175, 5R01ES024992, 2U01CA200060, U24ES026699, U01 HG009391 and American Cancer Society Research Scholar grant RSG-14-049-01-DMC.
Publisher Copyright:
© 2017 WILEY Periodicals, Inc.
PY - 2018/1
Y1 - 2018/1
N2 - Transposable elements (TEs) are no longer considered to be “junk” DNA. Here, we review how TEs can impact gene regulation systematically. TEs encode various regulatory elements that enables them to regulate gene expression. RJ Britten and EH Davidson hypothesized that TEs can integrate the function of various transcriptional regulators into gene regulatory networks. Uniquely TEs can deposit regulatory sites across the genome when they transpose, and thereby bring multiple genes under control of the same regulatory logic. Several studies together have robustly established that TEs participate in embryonic development and oncogenesis. We discuss the regulatory characteristics of TEs in context of evolution to understand the extent of their impact on gene networks. Understanding these features of TEs is central to future investigations of TEs in cellular processes and phenotypic presentations, which are applicable to development and disease studies. We re-visit the Britten–Davidson “gene-battery” model and understand the genetic and transcriptional impact of TEs in innovating gene regulatory networks.
AB - Transposable elements (TEs) are no longer considered to be “junk” DNA. Here, we review how TEs can impact gene regulation systematically. TEs encode various regulatory elements that enables them to regulate gene expression. RJ Britten and EH Davidson hypothesized that TEs can integrate the function of various transcriptional regulators into gene regulatory networks. Uniquely TEs can deposit regulatory sites across the genome when they transpose, and thereby bring multiple genes under control of the same regulatory logic. Several studies together have robustly established that TEs participate in embryonic development and oncogenesis. We discuss the regulatory characteristics of TEs in context of evolution to understand the extent of their impact on gene networks. Understanding these features of TEs is central to future investigations of TEs in cellular processes and phenotypic presentations, which are applicable to development and disease studies. We re-visit the Britten–Davidson “gene-battery” model and understand the genetic and transcriptional impact of TEs in innovating gene regulatory networks.
KW - gene regulation
KW - transposable elements
UR - http://www.scopus.com/inward/record.url?scp=85037350630&partnerID=8YFLogxK
U2 - 10.1002/bies.201700155
DO - 10.1002/bies.201700155
M3 - Article
C2 - 29206283
AN - SCOPUS:85037350630
SN - 0265-9247
VL - 40
JO - BioEssays
JF - BioEssays
IS - 1
M1 - 1700155
ER -