TY - JOUR
T1 - Impact of the gut microbiota on enhancer accessibility in gut intraepithelial lymphocytes
AU - Semenkovich, Nicholas P.
AU - Planer, Joseph D.
AU - Ahern, Philip P.
AU - Griffin, Nicholas W.
AU - Lin, Charles Y.
AU - Gordon, Jeffrey I.
N1 - Funding Information:
We thank Jessica Hoisington-Lopez for assistance with DNA sequencing, David O'Donnell and Maria Karlsson for help with gnotobiotic mouse husbandry, and Drew Hughes for valuable insights about the analytical approach. This work was supported in part by NIH Grants DK30292, DK70977, and DK078669. N.P.S. is supported by NIH Grant T32HG000045. N.P.S. and J.D.P. are members of the Washington University Medical Scientist Training Program supported by NIH Grant GM007200. P.P.A. is the recipient of a Sir Henry Wellcome Postdoctoral Fellowship (096100).
Publisher Copyright:
© 2016, National Academy of Sciences. All rights reserved.
PY - 2016/12/20
Y1 - 2016/12/20
N2 - The gut microbiota impacts many aspects of host biology including immune function. One hypothesis is that microbial communities induce epigenetic changes with accompanying alterations in chromatin accessibility, providing a mechanism that allows a community to have sustained host effects even in the face of its structural or functional variation. We used Assay for Transposase-Accessible Chromatin with high-throughput sequencing (ATAC-seq) to define chromatin accessibility in predicted enhancer regions of intestinal αβ+ and γδ+ intraepithelial lymphocytes purified from germ-free mice, their conventionally raised (CONV-R) counterparts, and mice reared germ free and then colonized with CONV-R gut microbiota at the end of the suckling-weaning transition. Characterizing genes adjacent to traditional enhancers and super-enhancers revealed signaling networks, metabolic pathways, and enhancer-associated transcription factors affected by the microbiota. Our results support the notion that epigenetic modifications help define microbial community-affiliated functional features of host immune cell lineages.
AB - The gut microbiota impacts many aspects of host biology including immune function. One hypothesis is that microbial communities induce epigenetic changes with accompanying alterations in chromatin accessibility, providing a mechanism that allows a community to have sustained host effects even in the face of its structural or functional variation. We used Assay for Transposase-Accessible Chromatin with high-throughput sequencing (ATAC-seq) to define chromatin accessibility in predicted enhancer regions of intestinal αβ+ and γδ+ intraepithelial lymphocytes purified from germ-free mice, their conventionally raised (CONV-R) counterparts, and mice reared germ free and then colonized with CONV-R gut microbiota at the end of the suckling-weaning transition. Characterizing genes adjacent to traditional enhancers and super-enhancers revealed signaling networks, metabolic pathways, and enhancer-associated transcription factors affected by the microbiota. Our results support the notion that epigenetic modifications help define microbial community-affiliated functional features of host immune cell lineages.
KW - ATAC-seq
KW - Enhancers of gut intraepithelial lymphocytes
KW - Gnotobiotic mice
KW - Gut microbiota-immune cell interactions
KW - Transcription factors
UR - http://www.scopus.com/inward/record.url?scp=85006930186&partnerID=8YFLogxK
U2 - 10.1073/pnas.1617793113
DO - 10.1073/pnas.1617793113
M3 - Article
C2 - 27911843
AN - SCOPUS:85006930186
SN - 0027-8424
VL - 113
SP - 14805
EP - 14810
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 51
ER -