High-Resolution Analysis of Parent-of-Origin Allelic Expression in the Mouse Brain

被引:396
作者
Gregg, Christopher [1 ,2 ]
Zhang, Jiangwen [3 ]
Weissbourd, Brandon [1 ,2 ]
Luo, Shujun [5 ]
Schroth, Gary P. [5 ]
Haig, David [4 ]
Dulac, Catherine [1 ,2 ]
机构
[1] Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA
[2] Harvard Univ, Howard Hughes Med Inst, Cambridge, MA 02138 USA
[3] Harvard Univ, FAS Res Comp, Cambridge, MA 02138 USA
[4] Harvard Univ, Dept Organism & Evolutionary Biol, Cambridge, MA 02138 USA
[5] Illumina Inc, Hayward, CA 94545 USA
关键词
IMPRINTED GENE; H19; IGF2; POLYADENYLATION; IDENTIFICATION; MECHANISMS; MUTATION; CELLS;
D O I
10.1126/science.1190830
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
Genomic imprinting results in preferential expression of the paternal or maternal allele of certain genes. We have performed a genome-wide characterization of imprinting in the mouse embryonic and adult brain. This approach uncovered parent-of-origin allelic effects of more than 1300 loci. We identified parental bias in the expression of individual genes and of specific transcript isoforms, with differences between brain regions. Many imprinted genes are expressed in neural systems associated with feeding and motivated behaviors, and parental biases preferentially target genetic pathways governing metabolism and cell adhesion. We observed a preferential maternal contribution to gene expression in the developing brain and a major paternal contribution in the adult brain. Thus, parental expression bias emerges as a major mode of epigenetic regulation in the brain.
引用
收藏
页码:643 / 648
页数:6
相关论文
共 46 条
[1]   DISTRIBUTION OF PARTHENOGENETIC CELLS IN THE MOUSE-BRAIN AND THEIR INFLUENCE ON BRAIN-DEVELOPMENT AND BEHAVIOR [J].
ALLEN, ND ;
LOGAN, K ;
LALLY, G ;
DRAGE, DJ ;
NORRIS, ML ;
KEVERNE, EB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (23) :10782-10786
[2]   Conserved methylation imprints in the human and mouse GRB10 genes with divergent allelic expression suggests differential reading of the same mark [J].
Arnaud, P ;
Monk, D ;
Hitchins, M ;
Gordon, E ;
Dean, W ;
Beechey, CV ;
Peters, J ;
Craigen, W ;
Preece, M ;
Stanier, P ;
Moore, GE ;
Kelsey, G .
HUMAN MOLECULAR GENETICS, 2003, 12 (09) :1005-1019
[3]   Global Survey of Genomic Imprinting by Transcriptome Sequencing [J].
Babak, Tomas ;
DeVeale, Brian ;
Armour, Christopher ;
Raymond, Christopher ;
Cleary, Michele A. ;
van der Kooy, Derek ;
Johnson, Jason M. ;
Lim, Lee P. .
CURRENT BIOLOGY, 2008, 18 (22) :1735-1741
[4]   Maternally inherited Birk barel mental retardation dysmorphism syndrome caused by a mutation in the genomically imprinted potassium channel KCNK9 [J].
Barel, Ortal ;
Shalev, Stavit A. ;
Ofir, Rivka ;
Cohen, Asi ;
Zlotogora, Joel ;
Shorer, Zamir ;
Mazor, Galia ;
Finer, Gal ;
Khateeb, Shareef ;
Zilberberg, Noam ;
Birk, Ohad S. .
AMERICAN JOURNAL OF HUMAN GENETICS, 2008, 83 (02) :193-199
[5]   Genomic imprinting in mammals [J].
Bartolomei, MS ;
Tilghman, SM .
ANNUAL REVIEW OF GENETICS, 1997, 31 :493-525
[6]   PARENTAL IMPRINTING OF THE MOUSE H19 GENE [J].
BARTOLOMEI, MS ;
ZEMEL, S ;
TILGHMAN, SM .
NATURE, 1991, 351 (6322) :153-155
[7]   EPIGENETIC MECHANISMS UNDERLYING THE IMPRINTING OF THE MOUSE H19-GENE [J].
BARTOLOMEI, MS ;
WEBBER, AL ;
BRUNKOW, ME ;
TILGHMAN, SM .
GENES & DEVELOPMENT, 1993, 7 (09) :1663-1673
[8]   The landscape of somatic copy-number alteration across human cancers [J].
Beroukhim, Rameen ;
Mermel, Craig H. ;
Porter, Dale ;
Wei, Guo ;
Raychaudhuri, Soumya ;
Donovan, Jerry ;
Barretina, Jordi ;
Boehm, Jesse S. ;
Dobson, Jennifer ;
Urashima, Mitsuyoshi ;
Mc Henry, Kevin T. ;
Pinchback, Reid M. ;
Ligon, Azra H. ;
Cho, Yoon-Jae ;
Haery, Leila ;
Greulich, Heidi ;
Reich, Michael ;
Winckler, Wendy ;
Lawrence, Michael S. ;
Weir, Barbara A. ;
Tanaka, Kumiko E. ;
Chiang, Derek Y. ;
Bass, Adam J. ;
Loo, Alice ;
Hoffman, Carter ;
Prensner, John ;
Liefeld, Ted ;
Gao, Qing ;
Yecies, Derek ;
Signoretti, Sabina ;
Maher, Elizabeth ;
Kaye, Frederic J. ;
Sasaki, Hidefumi ;
Tepper, Joel E. ;
Fletcher, Jonathan A. ;
Tabernero, Josep ;
Baselga, Jose ;
Tsao, Ming-Sound ;
Demichelis, Francesca ;
Rubin, Mark A. ;
Janne, Pasi A. ;
Daly, Mark J. ;
Nucera, Carmelo ;
Levine, Ross L. ;
Ebert, Benjamin L. ;
Gabriel, Stacey ;
Rustgi, Anil K. ;
Antonescu, Cristina R. ;
Ladanyi, Marc ;
Letai, Anthony .
NATURE, 2010, 463 (7283) :899-905
[9]   Alterations in CDH15 and KIRREL3 in Patients with Mild to Severe Intellectual Disability [J].
Bhalla, Kavita ;
Luo, Yue ;
Buchan, Tim ;
Beachem, Michael A. ;
Guzauskas, Gregory F. ;
Ladd, Sydney ;
Bratcher, Shelly J. ;
Schroer, Richard J. ;
Balsamo, Janne ;
DuPont, Barbara R. ;
Lillen, Jack ;
Srivastava, Anand K. .
AMERICAN JOURNAL OF HUMAN GENETICS, 2008, 83 (06) :703-713
[10]   Looking for trouble: A search for developmental defects of the hypothalamus [J].
Caqueret, A ;
Yang, C ;
Duplan, S ;
Boucher, F ;
Michaud, JL .
HORMONE RESEARCH, 2005, 64 (05) :222-230