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Human Molecular Genetics Advance Access originally published online on September 14, 2005
Human Molecular Genetics 2005 14(Review Issue 2):R171-R181; doi:10.1093/hmg/ddi335
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© The Author 2005. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Interactome: gateway into systems biology

Michael E. Cusick1,*, Niels Klitgord1, Marc Vidal1,2 and David E. Hill1,2

1Center for Cancer Systems Biology and Department of Cancer Biology, Dana-Farber Cancer Institute, 44 Binney Street, Boston, MA 02115, USA and 2Department of Genetics, Harvard Medical School, Boston, MA 02115, USA

* To whom correspondence should be addressed. Tel: +1 6176323802; Fax: +1 6176325739; Email: Michael_cusick{at}dfci.harvard.edu; marc_vidal{at}dfci.harvard.edu; david_hill{at}dfci.harvard.edu

Received August 18, 2005; Accepted September 1, 2005

Protein–protein interactions are fundamental to all biological processes, and a comprehensive determination of all protein–protein interactions that can take place in an organism provides a framework for understanding biology as an integrated system. The availability of genome-scale sets of cloned open reading frames has facilitated systematic efforts at creating proteome-scale data sets of protein–protein interactions, which are represented as complex networks or ‘interactome’ maps. Protein–protein interaction mapping projects that follow stringent criteria, coupled with experimental validation in orthogonal systems, provide high-confidence data sets immanently useful for interrogating developmental and disease mechanisms at a system level as well as elucidating individual protein function and interactome network topology. Although far from complete, currently available maps provide insight into how biochemical properties of proteins and protein complexes are integrated into biological systems. Such maps are also a useful resource to predict the function(s) of thousands of genes.


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