This CEGS will use an innovative combination of approaches to address two fundamental questions in genome biology: What do our genes do, and where did we come from? Rapid progress in genomics has provided nearly complete sequences for several organisms. Comparative analysis suggests many fundamental pathways and gene networks are conserved between organisms. And yet, the morphology, behavior, physiology, and disease susceptibility of different species are obviously and profoundly different. What are the mechanisms that generate new functions for genes, new physiological traits, and the unique form and functions of different species? Has the great variety of life forms been created by changes in gene number, by alterations in the functional attributes of particular proteins, or by diversification of the regulatory mechanisms that control where and when genes are expressed? This CEGS proposes a pioneering analysis of vertebrate diversity using a combination of techniques from structural and functional genomic and traditional genetics in zebrafish and sticklebacks. The unique experimental advantages of these two models will make it possible to take complementary approaches. The """"""""bottom-up"""""""" approach will test the diversification in expression and genetic function of duplicated gene pairs, a major hallmark of the vertebrate genome. In situ hybridization analysis will be used to compare the expression patterns of 2500 genes. Morpholino knockout experiments will test how the functions of duplicated genes diverge, and generate a database of gene functions for many genes identified in sequencing projects. The complementary """"""""top-down"""""""" approach will begin with naturally occurring species of sticklebacks that show profound differences in size, anatomy, and physiological traits. Genetic crosses will be used to identify the number and location of genetic changes that create the anatomical and physiological differences between recently evolved species from different regions around the world. Development of genetic and physical mapping resources for sticklebacks will make it possible to identify the actual genes and mutations responsible for evolutionary change. Immediate data release, free access to reagents, and an annual summer training course in fish genomic and genetics will ensure that the innovative approaches and results from this research will be widely disseminated to the research community. This unique combination of approaches will establish a completely new and detailed understanding of the genomic mechanisms responsible for morphological and physiological differences between living forms.

Agency
National Institute of Health (NIH)
Institute
National Human Genome Research Institute (NHGRI)
Type
Specialized Center (P50)
Project #
5P50HG002568-02
Application #
6626049
Study Section
Special Emphasis Panel (ZHG1-HGR-P (J3))
Program Officer
Felsenfeld, Adam
Project Start
2002-04-19
Project End
2007-03-31
Budget Start
2003-08-01
Budget End
2004-03-31
Support Year
2
Fiscal Year
2003
Total Cost
$2,992,382
Indirect Cost
Name
Stanford University
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
009214214
City
Stanford
State
CA
Country
United States
Zip Code
94305
Thompson, Abbey C; Capellini, Terence D; Guenther, Catherine A et al. (2018) A novel enhancer near the Pitx1 gene influences development and evolution of pelvic appendages in vertebrates. Elife 7:
Lowe, Craig B; Sanchez-Luege, Nicelio; Howes, Timothy R et al. (2018) Detecting differential copy number variation between groups of samples. Genome Res 28:256-265
Marques, David A; Jones, Felicity C; Di Palma, Federica et al. (2018) Experimental evidence for rapid genomic adaptation to a new niche in an adaptive radiation. Nat Ecol Evol 2:1128-1138
Bay, Rachael A; Arnegard, Matthew E; Conte, Gina L et al. (2017) Genetic Coupling of Female Mate Choice with Polygenic Ecological Divergence Facilitates Stickleback Speciation. Curr Biol 27:3344-3349.e4
Indjeian, Vahan B; Kingman, Garrett A; Jones, Felicity C et al. (2016) Evolving New Skeletal Traits by cis-Regulatory Changes in Bone Morphogenetic Proteins. Cell 164:45-56
Conte, Gina L; Arnegard, Matthew E; Best, Jacob et al. (2015) Extent of QTL Reuse During Repeated Phenotypic Divergence of Sympatric Threespine Stickleback. Genetics 201:1189-200
O'Brown, Natasha M; Summers, Brian R; Jones, Felicity C et al. (2015) A recurrent regulatory change underlying altered expression and Wnt response of the stickleback armor plates gene EDA. Elife 4:e05290
Cleves, Phillip A; Ellis, Nicholas A; Jimenez, Monica T et al. (2014) Evolved tooth gain in sticklebacks is associated with a cis-regulatory allele of Bmp6. Proc Natl Acad Sci U S A 111:13912-7
Wilson, Benjamin A; Petrov, Dmitri A; Messer, Philipp W (2014) Soft selective sweeps in complex demographic scenarios. Genetics 198:669-84
Kumar, Maya E; Bogard, Patrick E; Espinoza, F HernĂ¡n et al. (2014) Mesenchymal cells. Defining a mesenchymal progenitor niche at single-cell resolution. Science 346:1258810

Showing the most recent 10 out of 58 publications