Lessons from modENCODE

被引:40
作者
Brown, James B. [1 ,2 ]
Celniker, Susan E. [2 ]
机构
[1] Univ Calif Berkeley, Dept Stat, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Dept Genome Dynam, Berkeley, CA 94720 USA
来源
ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS, VOL 16 | 2015年 / 16卷
关键词
Drosophila melanogaster; Caenorhabditis elegans; transcription; replication; epigenetics; regulation of gene expression; LONG NONCODING RNAS; C; ELEGANS; GENE-EXPRESSION; INTEGRATIVE ANALYSIS; TRANSCRIPTION FACTORS; FUNCTIONAL ELEMENTS; ENDOGENOUS SIRNAS; D; MELANOGASTER; SEQ EXPERIMENTS; MESSENGER-RNAS;
D O I
10.1146/annurev-genom-090413-025448
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学];
摘要
The modENCODE (Model Organism Encyclopedia of DNA Elements) Consortium aimed to map functional elements-including transcripts, chromatin marks, regulatory factor binding sites, and origins of DNA replication-in the model organisms Drosophila melanogaster and Caenorhabditis elegans. During its five-year span, the consortium conducted more than 2,000 genome-wide assays in developmentally staged animals, dissected tissues, and homogeneous cell lines. Analysis of these data sets provided foundational insights into genome, epigenome, and transcriptome structure and the evolutionary turnover of regulatory pathways. These studies facilitated a comparative analysis with similar data types produced by the ENCODE Consortium for human cells. Genome organization differs drastically in these distant species, and yet quantitative relationships among chromatin state, transcription, and cotranscriptional RNA processing are deeply conserved. Of the many biological discoveries of the modENCODE Consortium, we highlight insights that emerged from integrative studies. We focus on operational and scientific lessons that may aid future projects of similar scale or aims in other, emerging model systems.
引用
收藏
页码:31 / 53
页数:23
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