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Integration of biological data by kernels on graph nodes allows prediction of new genes involved in mitotic chromosome condensation

Integration of biological data by kernels on graph nodes allows prediction of new genes involved in mitotic chromosome condensation
Integration of biological data by kernels on graph nodes allows prediction of new genes involved in mitotic chromosome condensation
The advent of genome-wide RNA interference (RNAi)–based screens puts us in the position to identify genes for all functions human cells carry out. However, for many functions, assay complexity and cost make genome-scale knockdown experiments impossible. Methods to predict genes required for cell functions are therefore needed to focus RNAi screens from the whole genome on the most likely candidates. Although different bioinformatics tools for gene function prediction exist, they lack experimental validation and are therefore rarely used by experimentalists. To address this, we developed an effective computational gene selection strategy that represents public data about genes as graphs and then analyzes these graphs using kernels on graph nodes to predict functional relationships. To demonstrate its performance, we predicted human genes required for a poorly understood cellular function—mitotic chromosome condensation—and experimentally validated the top 100 candidates with a focused RNAi screen by automated microscopy. Quantitative analysis of the images demonstrated that the candidates were indeed strongly enriched in condensation genes, including the discovery of several new factors. By combining bioinformatics prediction with experimental validation, our study shows that kernels on graph nodes are powerful tools to integrate public biological data and predict genes involved in cellular functions of interest.
1059-1524
Hériché, Jean-Karim
03041d48-adf7-4410-bb2b-94c8e9def867
Lees, Jon G
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Morilla, Ian
49aaf397-e8dd-4b15-a773-e8c1ae46bf79
Walter, Thomas
82af239f-4bdd-4a3c-b910-2899fbaa8d19
Petrova, Boryana
4123cfb8-cccf-48e0-86d9-d3003b9eb33e
Roberti, M Julia
d2bad755-bc10-4994-ba41-02a7a6f7c1f5
Hossain, M. Julius
bba1b875-7604-462b-a55b-ba0b54f728e8
Adler, Priit
98f731da-d04c-45ac-8cee-9c133d0383e7
Fernández, Jose M.
77cf9e0c-d2b5-4188-a030-1de79f45f3af
Krallinger, Martin
3af34c79-0475-4194-81ed-5c29e91e2cf9
Haering, Christian H.
d431c2ea-1081-49c1-b6cd-bb7fbd2fe985
Vilo, Jaak
491cc3a3-b567-41e4-9ff4-1cdee6573327
Valencia, Alfonso
d5fe794c-a731-4840-abde-a55db8518908
Ranea, Juan A.
7f218a89-6b7c-421d-81c3-78e712ee12e1
Orengo, Christine
f75f273c-e5ca-42df-851e-5e9ababb9494
Ellenberg, Jan
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Hériché, Jean-Karim
03041d48-adf7-4410-bb2b-94c8e9def867
Lees, Jon G
9290754e-671b-4861-badd-a13dd41e6d95
Morilla, Ian
49aaf397-e8dd-4b15-a773-e8c1ae46bf79
Walter, Thomas
82af239f-4bdd-4a3c-b910-2899fbaa8d19
Petrova, Boryana
4123cfb8-cccf-48e0-86d9-d3003b9eb33e
Roberti, M Julia
d2bad755-bc10-4994-ba41-02a7a6f7c1f5
Hossain, M. Julius
bba1b875-7604-462b-a55b-ba0b54f728e8
Adler, Priit
98f731da-d04c-45ac-8cee-9c133d0383e7
Fernández, Jose M.
77cf9e0c-d2b5-4188-a030-1de79f45f3af
Krallinger, Martin
3af34c79-0475-4194-81ed-5c29e91e2cf9
Haering, Christian H.
d431c2ea-1081-49c1-b6cd-bb7fbd2fe985
Vilo, Jaak
491cc3a3-b567-41e4-9ff4-1cdee6573327
Valencia, Alfonso
d5fe794c-a731-4840-abde-a55db8518908
Ranea, Juan A.
7f218a89-6b7c-421d-81c3-78e712ee12e1
Orengo, Christine
f75f273c-e5ca-42df-851e-5e9ababb9494
Ellenberg, Jan
7b8ab9a9-8076-4db1-b7a2-8445accc9b54

Hériché, Jean-Karim, Lees, Jon G, Morilla, Ian, Walter, Thomas, Petrova, Boryana, Roberti, M Julia, Hossain, M. Julius, Adler, Priit, Fernández, Jose M., Krallinger, Martin, Haering, Christian H., Vilo, Jaak, Valencia, Alfonso, Ranea, Juan A., Orengo, Christine and Ellenberg, Jan (2014) Integration of biological data by kernels on graph nodes allows prediction of new genes involved in mitotic chromosome condensation. Molecular Biology of the Cell, 25 (16). (doi:10.1091/mbc.E13-04-0221).

Record type: Article

Abstract

The advent of genome-wide RNA interference (RNAi)–based screens puts us in the position to identify genes for all functions human cells carry out. However, for many functions, assay complexity and cost make genome-scale knockdown experiments impossible. Methods to predict genes required for cell functions are therefore needed to focus RNAi screens from the whole genome on the most likely candidates. Although different bioinformatics tools for gene function prediction exist, they lack experimental validation and are therefore rarely used by experimentalists. To address this, we developed an effective computational gene selection strategy that represents public data about genes as graphs and then analyzes these graphs using kernels on graph nodes to predict functional relationships. To demonstrate its performance, we predicted human genes required for a poorly understood cellular function—mitotic chromosome condensation—and experimentally validated the top 100 candidates with a focused RNAi screen by automated microscopy. Quantitative analysis of the images demonstrated that the candidates were indeed strongly enriched in condensation genes, including the discovery of several new factors. By combining bioinformatics prediction with experimental validation, our study shows that kernels on graph nodes are powerful tools to integrate public biological data and predict genes involved in cellular functions of interest.

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More information

Accepted/In Press date: 12 June 2014
e-pub ahead of print date: 18 June 2014
Published date: 15 August 2014
Additional Information: © 2014 Hériché et al.

Identifiers

Local EPrints ID: 458223
URI: http://eprints.soton.ac.uk/id/eprint/458223
ISSN: 1059-1524
PURE UUID: f0c52f5a-2356-42aa-bc8d-76dc70669a60
ORCID for M. Julius Hossain: ORCID iD orcid.org/0000-0003-3303-5755

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Date deposited: 01 Jul 2022 16:33
Last modified: 17 Mar 2024 04:12

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Contributors

Author: Jean-Karim Hériché
Author: Jon G Lees
Author: Ian Morilla
Author: Thomas Walter
Author: Boryana Petrova
Author: M Julia Roberti
Author: M. Julius Hossain ORCID iD
Author: Priit Adler
Author: Jose M. Fernández
Author: Martin Krallinger
Author: Christian H. Haering
Author: Jaak Vilo
Author: Alfonso Valencia
Author: Juan A. Ranea
Author: Christine Orengo
Author: Jan Ellenberg

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