Evidence map›Paper›PMID 20550706›Full record

ArticleBMC systems biology2010

Protein interaction network topology uncovers melanogenesis regulatory network components within functional genomics datasets.

Hsiang Ho, Tijana Milenković, Vesna Memisević, Jayavani Aruri, Natasa Przulj, Anand K Ganesan

Open access · diamondAbstract read
In one paragraph

Article in BMC systems biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.3field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 35 citations in OpenAlex.

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  8. Network science (Cambridge University Press) · 2014
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 2 countries.

Hsiang HoDepartment of Biological Chemistry, University of California, Irvine, 92697-1700, USA.
Tijana Milenković
Vesna Memisević
Jayavani Aruri
Natasa Przulj
Anand K Ganesan
University of California, Irvine · USUniversity of California, Berkeley · USImperial College London · GB

Funding

Aldehyde dehydrogenase: A novel regulator of melanin biogenesisK08AR056001 · NIAMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI GANESAN, ANAND K · 2009 to 2013
$551k
Dissecting the Impact of Autophagy Regulators on Melanogenesis in Normal Human CeR03AR057150 · NIAMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI GANESAN, ANAND K · 2009 to 2011
$203k
NIAMS NIH HHS 1K08AR056001-01A1NIAMS NIH HHS 1R03AR057150-01NIAMS NIH HHS K08 AR056001NIAMS NIH HHS R03 AR057150
6 · The paper itself

Abstract

backgroundRNA-mediated interference (RNAi)-based functional genomics is a systems-level approach to identify novel genes that control biological phenotypes. Existing computational approaches can identify individual genes from RNAi datasets that regulate a given biological process. However, currently available methods cannot identify which RNAi screen "hits" are novel components of well-characterized biological pathways known to regulate the interrogated phenotype. In this study, we describe a method to identify genes from RNAi datasets that are novel components of known biological pathways. We experimentally validate our approach in the context of a recently completed RNAi screen to identify novel regulators of melanogenesis.

resultsIn this study, we utilize a PPI network topology-based approach to identify targets within our RNAi dataset that may be components of known melanogenesis regulatory pathways. Our computational approach identifies a set of screen targets that cluster topologically in a human PPI network with the known pigment regulator Endothelin receptor type B (EDNRB). Validation studies reveal that these genes impact pigment production and EDNRB signaling in pigmented melanoma cells (MNT-1) and normal melanocytes.

conclusionsWe present an approach that identifies novel components of well-characterized biological pathways from functional genomics datasets that could not have been identified by existing statistical and computational approaches.

Indexed as

Models, BiologicalComputational BiologyGene Regulatory NetworksGenomicsHumansMelaninsMelanocytesProtein Interaction MappingReceptor, Endothelin BRNA InterferenceSignal TransductionMelaninsReceptor, Endothelin B

Identifiers

PMID20550706
PMCPMC2904735
OpenAlexW2114185968

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.