The spotted gar genome illuminates vertebrate evolution and facilitates human-teleost comparisons.

Nat Genet
Authors
Keywords
Abstract

To connect human biology to fish biomedical models, we sequenced the genome of spotted gar (Lepisosteus oculatus), whose lineage diverged from teleosts before teleost genome duplication (TGD). The slowly evolving gar genome has conserved in content and size many entire chromosomes from bony vertebrate ancestors. Gar bridges teleosts to tetrapods by illuminating the evolution of immunity, mineralization and development (mediated, for example, by Hox, ParaHox and microRNA genes). Numerous conserved noncoding elements (CNEs; often cis regulatory) undetectable in direct human-teleost comparisons become apparent using gar: functional studies uncovered conserved roles for such cryptic CNEs, facilitating annotation of sequences identified in human genome-wide association studies. Transcriptomic analyses showed that the sums of expression domains and expression levels for duplicated teleost genes often approximate the patterns and levels of expression for gar genes, consistent with subfunctionalization. The gar genome provides a resource for understanding evolution after genome duplication, the origin of vertebrate genomes and the function of human regulatory sequences.

Year of Publication
2016
Journal
Nat Genet
Volume
48
Issue
4
Pages
427-37
Date Published
2016 Apr
ISSN
1546-1718
URL
DOI
10.1038/ng.3526
PubMed ID
26950095
PubMed Central ID
PMC4817229
Links
Grant list
WT095908 / Wellcome Trust / United Kingdom
R24 OD010922 / OD / NIH HHS / United States
U54 HG003067 / HG / NHGRI NIH HHS / United States
U54 HG03067 / HG / NHGRI NIH HHS / United States
268513 / European Research Council / International
R01 GM079492 / GM / NIGMS NIH HHS / United States
R24 OD01119004 / OD / NIH HHS / United States
R01 AI057559 / AI / NIAID NIH HHS / United States
WT098051 / Wellcome Trust / United Kingdom
R01 RR020833 / RR / NCRR NIH HHS / United States
T32 HD055164 / HD / NICHD NIH HHS / United States
R01 OD011116 / OD / NIH HHS / United States