Functional networking of human divergently paired genes (DPGs).

Divergently paired genes (DPGs), also known as bidirectional (head-to-head positioned) genes, are conserved across species and lineages, and thus deemed to be exceptional in genomic organization and functional regulation. Despite previous investigations on the features of their conservation and gene...

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Main Authors: Bin Xie, Dapeng Wang, Yong Duan, Jun Yu, Hongxing Lei
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3815023?pdf=render
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spelling doaj-f4759cfe8be149b3bb62b2c46ac28b9a2020-11-25T01:24:02ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-01810e7889610.1371/journal.pone.0078896Functional networking of human divergently paired genes (DPGs).Bin XieDapeng WangYong DuanJun YuHongxing LeiDivergently paired genes (DPGs), also known as bidirectional (head-to-head positioned) genes, are conserved across species and lineages, and thus deemed to be exceptional in genomic organization and functional regulation. Despite previous investigations on the features of their conservation and gene organization, the functional relationship among DPGs in a given species and lineage has not been thoroughly clarified. Here we report a network-based comprehensive analysis on human DPGs and our results indicate that the two members of the DPGs tend to participate in different biological processes while enforcing related functions as modules. Comparing to randomly paired genes as a control, the DPG pairs have a tendency to be clustered in similar "cellular components" and involved in similar "molecular functions". The functional network bridged by DPGs consists of three major modules. The largest module includes many house-keeping genes involved in core cellular activities. This module also shows low variation in expression in both CNS (central nervous system) and non-CNS tissues. Based on analyses of disease transcriptome data, we further suggest that this particular module may play crucial roles in HIV infection and its disease mechanism.http://europepmc.org/articles/PMC3815023?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Bin Xie
Dapeng Wang
Yong Duan
Jun Yu
Hongxing Lei
spellingShingle Bin Xie
Dapeng Wang
Yong Duan
Jun Yu
Hongxing Lei
Functional networking of human divergently paired genes (DPGs).
PLoS ONE
author_facet Bin Xie
Dapeng Wang
Yong Duan
Jun Yu
Hongxing Lei
author_sort Bin Xie
title Functional networking of human divergently paired genes (DPGs).
title_short Functional networking of human divergently paired genes (DPGs).
title_full Functional networking of human divergently paired genes (DPGs).
title_fullStr Functional networking of human divergently paired genes (DPGs).
title_full_unstemmed Functional networking of human divergently paired genes (DPGs).
title_sort functional networking of human divergently paired genes (dpgs).
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description Divergently paired genes (DPGs), also known as bidirectional (head-to-head positioned) genes, are conserved across species and lineages, and thus deemed to be exceptional in genomic organization and functional regulation. Despite previous investigations on the features of their conservation and gene organization, the functional relationship among DPGs in a given species and lineage has not been thoroughly clarified. Here we report a network-based comprehensive analysis on human DPGs and our results indicate that the two members of the DPGs tend to participate in different biological processes while enforcing related functions as modules. Comparing to randomly paired genes as a control, the DPG pairs have a tendency to be clustered in similar "cellular components" and involved in similar "molecular functions". The functional network bridged by DPGs consists of three major modules. The largest module includes many house-keeping genes involved in core cellular activities. This module also shows low variation in expression in both CNS (central nervous system) and non-CNS tissues. Based on analyses of disease transcriptome data, we further suggest that this particular module may play crucial roles in HIV infection and its disease mechanism.
url http://europepmc.org/articles/PMC3815023?pdf=render
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