Novel MicroRNA Regulators of Atrial Natriuretic Peptide Production

被引:17
|
作者
Wu, Connie [1 ,2 ,3 ]
Arora, Pankaj [4 ]
Agha, Obiajulu [2 ]
Hurst, Liam A. [2 ]
Allen, Kaitlin [2 ]
Nathan, Daniel I. [2 ]
Hu, Dongjian [1 ,5 ]
Jiramongkolchai, Pawina [2 ]
Smith, J. Gustav [1 ,3 ,6 ,7 ,8 ]
Melander, Olle [9 ,10 ]
Trenson, Sander [11 ]
Janssens, Stefan P. [11 ]
Domian, Ibrahim [1 ,12 ]
Wang, Thomas J. [13 ]
Bloch, Kenneth D. [1 ,2 ]
Buys, Emmanuel S. [2 ]
Bloch, Donald B. [2 ,14 ]
Newton-Cheh, Christopher [1 ,3 ,6 ]
机构
[1] Massachusetts Gen Hosp, Harvard Med Sch, Dept Med, Cardiovasc Res Ctr, Boston, MA 02114 USA
[2] Massachusetts Gen Hosp, Harvard Med Sch, Dept Anesthesia Crit Care & Pain Med, Anesthesia Ctr Crit Care Res, Boston, MA 02114 USA
[3] Broad Inst, Program Med & Populat Genet, Cambridge, MA USA
[4] Univ Alabama Birmingham, Dept Med, Div Cardiol, Birmingham, AL 35294 USA
[5] Boston Univ, Dept Biomed Engn, Boston, MA 02215 USA
[6] Massachusetts Gen Hosp, Harvard Med Sch, Ctr Human Genet Res, Boston, MA 02114 USA
[7] Lund Univ, Dept Cardiol, Clin Sci, Lund, Sweden
[8] Skane Univ Hosp, Dept Heart Failure & Valvular Dis, Lund, Sweden
[9] Lund Univ, Dept Internal Med, Clin Sci, Malmo, Sweden
[10] Skane Univ Hosp, Malmo, Sweden
[11] Univ Leuven, Dept Cardiovasc Sci, Leuven, Belgium
[12] Harvard Stem Cell Inst, Cambridge, MA USA
[13] Vanderbilt Univ, Sch Med, Dept Med, Div Cardiovasc Med, Nashville, TN 37212 USA
[14] Massachusetts Gen Hosp, Dept Med, Div Rheumatol Allergy & Immunol, Harvard Med Sch, Boston, MA 02114 USA
基金
美国国家卫生研究院;
关键词
CELL-DERIVED CARDIOMYOCYTE; PLURIPOTENT STEM-CELLS; CARDIAC-HYPERTROPHY; MESSENGER-RNA; HEART-TISSUE; EXPRESSION; DIFFERENTIATION; FAILURE; TARGETS;
D O I
10.1128/MCB.01114-15
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Atrial natriuretic peptide (ANP) has a central role in regulating blood pressure in humans. Recently, microRNA 425 (miR-425) was found to regulate ANP production by binding to the mRNA of NPPA, the gene encoding ANP. mRNAs typically contain multiple predicted microRNA (miRNA)-binding sites, and binding of different miRNAs may independently or coordinately regulate the expression of any given mRNA. We used a multifaceted screening strategy that integrates bioinformatics, next-generation sequencing data, human genetic association data, and cellular models to identify additional functional NPPA-targeting miRNAs. Two novel miRNAs, miR-155 and miR-105, were found to modulate ANP production in human cardiomyocytes and target genetic variants whose minor alleles are associated with higher human plasma ANP levels. Both miR-155 and miR-105 repressed NPPA mRNA in an allele-specific manner, with the minor allele of each respective variant conferring resistance to the miRNA either by disruption of miRNA base pairing or by creation of wobble base pairing. Moreover, miR-155 enhanced the repressive effects of miR-425 on ANP production in human cardiomyocytes. Our study combines computational, genomic, and cellular tools to identify novel miRNA regulators of ANP production that could be targeted to raise ANP levels, which may have applications for the treatment of hypertension or heart failure.
引用
收藏
页码:1977 / 1987
页数:11
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