ZFIN ID: ZDB-PUB-140224-41
Time for the zebrafish ENCODE
Sivasubbu, S., Sachidanandan, C., and Scaria, V.
Date: 2013
Source: Journal of genetics   92(3): 695-701 (Journal)
Registered Authors: Sachidanandan, Chetana, Sivasubbu, Sridhar
Keywords: none
MeSH Terms:
  • Animals
  • Databases, Genetic*
  • Genomics
  • Humans
  • Information Dissemination
  • Zebrafish/genetics*
PubMed: 24371190 Full text @ J. Genet.

Genomics research in recent years, especially the human ENCODE project, have made great strides in understanding the genomic and epigenomic structure and organization of humans. These advances promise a new era of precision medicine, through a better understanding of the genomic correlates of human physiology and promise to offer precise and personalized preventive and therapeutic options. The translation of genome-scale maps of genomic and epigenomic markers to clinically relevant information and further to medical practice await functional validation of the genomic features identified through these large-scale efforts. Such studies must essentially be done in model systems where it is possible to model physiological and pathological processes and enquire how they could be modulated by genomic elements and epigenomic signatures. The availability of large number of personal genomes and maps of genomic variations at population scale has created an acute necessity for model systems to model phenotypic and molecular effects of variations, especially in regulatory regions. Efforts to create orthologous maps have been underway in other model systems including Caenorhabditis elegans and Drosophila through the modENCODE programe and in Mus musculus through the mouse ENCODE. We propose that the enormous wealth of disease models and excellent tools to engineer genomes in zebrafish could be effectively capitalized towards making it an effective and widely used model system for precision medicine. This would be possible only through a concerted and systematic effort to create orthologous genomic and epigenomic maps for zebrafish.We discuss how the present understanding and genome-scale methodologies available in this model organism could be effectively used towards realizing this goal.