Authors

J. Fan; J. G. Dy; C. C. Chang;X. B. Zhou

Comments

Authors: contact us about adding a copy of your work at STARS@ucf.edu

Abbreviated Journal Title

Chin. J. Cancer

Keywords

Association study; genetic variation and mutation; transcription; factor-binding sites; myelodysplastic syndromes; GENOME-WIDE ASSOCIATION; CHROMOSOMAL-ABNORMALITIES; UNIPARENTAL DISOMY; VARIABLE SELECTION; REGRESSION; LOCI; MICROARRAYS; POPULATION; VARIANTS; PROFILES; Oncology

Abstract

Myelodysplastic syndromes have increased in frequency and incidence in the American population, but patient prognosis has not significantly improved over the last decade. Such improvements could be realized if biomarkers for accurate diagnosis and prognostic stratification were successfully identified. In this study, we propose a method that associates two state-of-the-art array technologies-single nucleotide polymor-phism (SNP) array and gene expression array-with gene motifs considered transcription factor-binding sites (TFBS). We are particularly interested in SNP-containing motifs introduced by genetic variation and mutation as TFBS. The potential regulation of SNP-containing motifs affects only when certain mutations occur. These motifs can be identified from a group of co-expressed genes with copy number variation. Then, we used a sliding window to identify motif candidates near SNPs on gene sequences. The candidates were filtered by coarse thresholding and fine statistical testing. Using the regression. based LARS-EN algorithm and a level. wise sequence combination procedure, we identified 28 SNP-containing motifs as candidate TFBS. We confirmed 21 of the 28 motifs with ChIP-chip fragments in the TRANSFAC database. Another six motifs were validated by TRANSFAC via searching binding fragments on co-regulated genes. The identified motifs and their location genes can be considered potential biomarkers for myelodysplastic syndromes. Thus, our proposed method, a novel strategy for associating two data categories, is capable of integrating information from different sources to identify reliable candidate regulatory SNP-containing motifs introduced by genetic variation and mutation.

Journal Title

Chinese Journal of Cancer

Volume

32

Issue/Number

4

Publication Date

1-1-2013

Document Type

Article

Language

English

First Page

170

Last Page

185

WOS Identifier

WOS:000339648500004

ISSN

1000-467X

Share

COinS