The goal of the present study was to narrow a region of chromosome 13 to only several genes and then apply unbiased statistical approaches to identify molecular networks and biological pathways relevant to blood pressure salt sensitivity in Dahl salt-sensitive (SS) rats. The analysis of 13 overlapping subcongenic strains identified a 1.37 Mbp region on chromosome 13 that influenced the mean arterial blood pressure by at least 25 mmHg in SS rats fed a high-salt diet. DNA sequencing and analysis filled genomic gaps and provided identification of five genes in this region, Rfwd2, Fam5b, Astn1, Pappa2, and Tnr. A crossplatform normalization of transcriptome data sets obtained from our previously published Affymetrix GeneChip dataset and newly acquired RNA-seq data from renal outer medullary tissue provided 90 observations for each gene. Two Bayesian methods were used to analyze the data: 1) a linear model analysis to assess 243 biological pathways for their likelihood to discriminate blood pressure levels across experimental groups and 2) a Bayesian graphical modeling of pathways to discover genes with potential relationships to the candidate genes in this region. As none of these five genes are known to be involved in hypertension, this unbiased approach has provided useful clues to be experimentally explored. Of these five genes, Rfwd2, the gene most strongly expressed in the renal outer medulla, was notably associated with pathways that can affect blood pressure via renal transcellular Na and K electrochemical gradients and tubular Na transport, mitochondrial TCA cycle and cell energetics, and circadian rhythms.

Characterization of biological pathways associated with a 1.37 Mbp genomic region protective of hypertension in Dahl S rats / Allen W, Cowley Jr.; Moreno, Carol; Jacob, Howard J.; Peterson, Christine B.; Stingo, Francesco C.; Ahn, Kwang Woo; Liu, Pengyuan; Vannucci, Marina; Laud, Purushottam W.; Reddy, Prajwal; Lazar, Jozef; Evans, Louise; Yang, Chun; Kurth, Theresa; Liang, Mingyu. - In: PHYSIOLOGICAL GENOMICS. - ISSN 1094-8341. - STAMPA. - 46:(2014), pp. 398-410. [10.1152/physiolgenomics.00179.2013]

Characterization of biological pathways associated with a 1.37 Mbp genomic region protective of hypertension in Dahl S rats

STINGO, FRANCESCO CLAUDIO;
2014

Abstract

The goal of the present study was to narrow a region of chromosome 13 to only several genes and then apply unbiased statistical approaches to identify molecular networks and biological pathways relevant to blood pressure salt sensitivity in Dahl salt-sensitive (SS) rats. The analysis of 13 overlapping subcongenic strains identified a 1.37 Mbp region on chromosome 13 that influenced the mean arterial blood pressure by at least 25 mmHg in SS rats fed a high-salt diet. DNA sequencing and analysis filled genomic gaps and provided identification of five genes in this region, Rfwd2, Fam5b, Astn1, Pappa2, and Tnr. A crossplatform normalization of transcriptome data sets obtained from our previously published Affymetrix GeneChip dataset and newly acquired RNA-seq data from renal outer medullary tissue provided 90 observations for each gene. Two Bayesian methods were used to analyze the data: 1) a linear model analysis to assess 243 biological pathways for their likelihood to discriminate blood pressure levels across experimental groups and 2) a Bayesian graphical modeling of pathways to discover genes with potential relationships to the candidate genes in this region. As none of these five genes are known to be involved in hypertension, this unbiased approach has provided useful clues to be experimentally explored. Of these five genes, Rfwd2, the gene most strongly expressed in the renal outer medulla, was notably associated with pathways that can affect blood pressure via renal transcellular Na and K electrochemical gradients and tubular Na transport, mitochondrial TCA cycle and cell energetics, and circadian rhythms.
2014
46
398
410
Allen W, Cowley Jr.; Moreno, Carol; Jacob, Howard J.; Peterson, Christine B.; Stingo, Francesco C.; Ahn, Kwang Woo; Liu, Pengyuan; Vannucci, Marina; Laud, Purushottam W.; Reddy, Prajwal; Lazar, Jozef; Evans, Louise; Yang, Chun; Kurth, Theresa; Liang, Mingyu
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/1054967
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