Literature DB >> 22323457

iSyTE: integrated Systems Tool for Eye gene discovery.

Salil A Lachke1, Joshua W K Ho, Gregory V Kryukov, Daniel J O'Connell, Anton Aboukhalil, Martha L Bulyk, Peter J Park, Richard L Maas.   

Abstract

PURPOSE: To facilitate the identification of genes associated with cataract and other ocular defects, the authors developed and validated a computational tool termed iSyTE (integrated Systems Tool for Eye gene discovery; http://bioinformatics.udel.edu/Research/iSyTE). iSyTE uses a mouse embryonic lens gene expression data set as a bioinformatics filter to select candidate genes from human or mouse genomic regions implicated in disease and to prioritize them for further mutational and functional analyses.
METHODS: Microarray gene expression profiles were obtained for microdissected embryonic mouse lens at three key developmental time points in the transition from the embryonic day (E)10.5 stage of lens placode invagination to E12.5 lens primary fiber cell differentiation. Differentially regulated genes were identified by in silico comparison of lens gene expression profiles with those of whole embryo body (WB) lacking ocular tissue.
RESULTS: Gene set analysis demonstrated that this strategy effectively removes highly expressed but nonspecific housekeeping genes from lens tissue expression profiles, allowing identification of less highly expressed lens disease-associated genes. Among 24 previously mapped human genomic intervals containing genes associated with isolated congenital cataract, the mutant gene is ranked within the top two iSyTE-selected candidates in approximately 88% of cases. Finally, in situ hybridization confirmed lens expression of several novel iSyTE-identified genes.
CONCLUSIONS: iSyTE is a publicly available Web resource that can be used to prioritize candidate genes within mapped genomic intervals associated with congenital cataract for further investigation. Extension of this approach to other ocular tissue components will facilitate eye disease gene discovery.

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Year:  2012        PMID: 22323457      PMCID: PMC3339920          DOI: 10.1167/iovs.11-8839

Source DB:  PubMed          Journal:  Invest Ophthalmol Vis Sci        ISSN: 0146-0404            Impact factor:   4.799


  64 in total

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10.  A new locus for autosomal recessive congenital cataract identified in a Pakistani family.

Authors:  Haiba Kaul; S Amer Riazuddin; Afshan Yasmeen; Sadia Mohsin; Mohsin Khan; Idrees A Nasir; Shaheen N Khan; Tayyab Husnain; Javed Akram; J Fielding Hejtmancik; Sheikh Riazuddin
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  61 in total

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3.  N-myc regulates growth and fiber cell differentiation in lens development.

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4.  Loss of Sip1 leads to migration defects and retention of ectodermal markers during lens development.

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5.  Deficiency of the RNA binding protein caprin2 causes lens defects and features of Peters anomaly.

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7.  Compound mouse mutants of bZIP transcription factors Mafg and Mafk reveal a regulatory network of non-crystallin genes associated with cataract.

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Review 8.  Application of a systems approach to study developmental gene regulation.

Authors:  Joshua W K Ho
Journal:  Biophys Rev       Date:  2012-09-01

9.  RNA sequencing-based transcriptomic profiles of embryonic lens development for cataract gene discovery.

Authors:  Deepti Anand; Atul Kakrana; Archana D Siddam; Hongzhan Huang; Irfan Saadi; Salil A Lachke
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Review 10.  Signaling and Gene Regulatory Networks in Mammalian Lens Development.

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