A Polymorphic 3’UTR Element in ATP1B1 Regulates Alternative Polyadenylation and Is Associated with Blood Pressure

Although variants in many genes have previously been shown to be associated with blood pressure (BP) levels, the molecular mechanism underlying these associations are mostly unknown. We identified a multi-allelic T-rich sequence (TRS) in the 3'UTR of ATP1B1 that varies in length and sequence co...

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Veröffentlicht in:PloS one Jg. 8; H. 10; S. e76290
Hauptverfasser: Prasad, Megana K., Bhalla, Kavita, Pan, Zhen Hua, O’Connell, Jeffrey R., Weder, Alan B., Chakravarti, Aravinda, Tian, Bin, Chang, Yen-Pei C.
Format: Journal Article
Sprache:Englisch
Veröffentlicht: United States Public Library of Science 01.10.2013
Public Library of Science (PLoS)
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ISSN:1932-6203, 1932-6203
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Zusammenfassung:Although variants in many genes have previously been shown to be associated with blood pressure (BP) levels, the molecular mechanism underlying these associations are mostly unknown. We identified a multi-allelic T-rich sequence (TRS) in the 3'UTR of ATP1B1 that varies in length and sequence composition (T22-27 and T12GT 3GT6). The 3'UTR of ATP1B1 contains 2 functional polyadenylation signals and the TRS is downstream of the proximal polyadenylation site (A2). Therefore, we hypothesized that alleles of this TRS might influence ATP1B1 expression by regulating alternative polyadenylation. In vitro, the T12GT 3GT6 allele increases polyadenylation at the A2 polyadenylation site as compared to the T23 allele. Consistent with our hypothesis, the relative abundance of the A2-polyadenylated ATP1B1 mRNA was higher in human kidneys with at least one copy of the T12GT 3GT6 allele than in those lacking this allele. The T12GT 3GT6 allele is also associated with higher systolic BP (beta = 3.3 mmHg, p = 0.014) and diastolic BP (beta = 2.4 mmHg, p = 0.003) in a European-American population. Therefore, we have identified a novel multi-allelic TRS in the 3'UTR of ATP1B1 that is associated with higher BP and may mediate its effect by regulating the polyadenylation of the ATP1B1 mRNA.
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Conceived and designed the experiments: MKP KB ZP BT YCC. Performed the experiments: MKP KB ZP. Analyzed the data: MKP KB JRO YCC. Contributed reagents/materials/analysis tools: JRO ABW AC BT. Wrote the manuscript: MKP YCC.
Competing Interests: The authors have declared that no competing interests exist.
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0076290