Insights from Chromosome-Centric Mapping of Disease-Associated Genes: Chromosome 12 Perspective.

Abstract:

:In line with the aims of the Chromosome-based Human Proteome Project and the Biology/Disease-based Human Proteome Project, we have been studying differentially expressed transcripts and proteins in gliomas—the most prevalent primary brain tumors. Here, we present a perspective on important insights from this analysis in terms of their co-expression, co-regulation/de-regulation, and co-localization on chromosome 12 (Chr. 12). We observe the following: (1) Over-expression of genes mapping onto amplicon regions of chromosomes may be considered as a biological validation of mass spectrometry data. (2) Their co-localization further suggests common determinants of co-expression and co-regulation of these clusters. (3) Co-localization of "missing" protein genes of Chr. 12 in close proximity to functionally related genes may help in predicting their functions. (4) Further, integrating differentially expressed gene-protein sets and their ontologies with medical terms associated with clinical phenotypes in a chromosome-centric manner reveals a network of genes, diseases, and pathways—a diseasome network. Thus, chromosomal mapping of disease data sets can help uncover important regulatory and functional links that may offer new insights for biomarker development.

journal_name

J Proteome Res

authors

Jayaram S,Gupta MK,Shivakumar BM,Ghatge M,Sharma A,Vangala RK,Sirdeshmukh R

doi

10.1021/acs.jproteome.5b00488

subject

Has Abstract

pub_date

2015-09-04 00:00:00

pages

3432-40

issue

9

eissn

1535-3893

issn

1535-3907

journal_volume

14

pub_type

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