An Intricate Network of Conserved DNA Upstream Motifs and Associated Transcription Factors Regulate the Expression of Uromodulin Gene

被引:15
作者
Srivastava, Rajneesh [1 ]
Micanovic, Radmila [2 ,5 ]
El-Achkar, Tarek M. [2 ,5 ]
Janga, Sarath Chandra [1 ,3 ,4 ]
机构
[1] Indiana Univ Purdue Univ, Sch Informat & Comp, Dept Biohlth Informat, Indianapolis, IN 46202 USA
[2] Indiana Univ, Sch Med, Dept Med, Div Nephrol, Indianapolis, IN 46202 USA
[3] Indiana Univ, Sch Med, Dept Med & Mol Genet, Indianapolis, IN 46202 USA
[4] Indiana Univ, Sch Med, Ctr Computat Biol & Bioinformat, Indianapolis, IN 46202 USA
[5] Roudebush Vet Affairs Med Ctr, Indianapolis, IN USA
关键词
kidney; computational biology; gene expression regulation; uromodulin; transcription factors; TAMM-HORSFALL PROTEIN; BINDING-SITES; DISCOVERY; ELEMENTS; INJURY;
D O I
10.1016/j.juro.2014.02.095
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Purpose: Uromodulin is a kidney specific glycoprotein whose expression can modulate kidney homeostasis. However, the set of sequence specific transcription factors that regulate the uromodulin gene UMOD and their upstream binding locations are not well characterized. We built a high resolution map of its transcriptional regulation. Materials and Methods: We applied in silico phylogenetic footprinting on the upstream regulatory regions of a diverse set of human UMOD orthologs to identify conserved binding motifs and corresponding position specific weight matrices. We further analyzed the predicted binding motifs by motif comparison, which identified transcription factors likely to bind these discovered motifs. Predicted transcription factors were then integrated with experimentally known protein-protein interactions available from public databases and tissue specific expression resources to delineate important regulators controlling UMOD expression. Results: Analysis allowed the identification of a reliable set of binding motifs in the upstream regulatory regions of UMOD to build a high confidence compendium of transcription factors that could bind these motifs, such as GATA3, HNF1B, SP1, SMAD3, RUNX2 and KLF4. ENCODE deoxyribonuclease I hypersensitivity sites in the UMOD upstream region of the mouse kidney confirmed that some of these binding motifs were open to binding by predicted transcription factors. The transcription factor-transcription factor network revealed several highly connected transcription factors, such as SP1, SP3, TP53, POU2F1, RARB, RARA and RXRA, as well as the likely protein complexes formed between them. Expression levels of these transcription factors in the kidney suggest their central role in controlling UMOD expression. Conclusions: Our findings will form a map for understanding the regulation of uromodulin expression in health and disease.
引用
收藏
页码:981 / 989
页数:9
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