CCR5AS lncRNA variation differentially regulates CCR5, influencing HIV disease outcome

被引:73
|
作者
Kulkarni, Smita [1 ,2 ,3 ]
Lied, Alexandra [2 ,3 ]
Kulkarni, Viraj [2 ,3 ]
Rucevic, Marijana [2 ,3 ,4 ]
Martin, Maureen P. [5 ]
Walker-Sperling, Victoria [6 ]
Anderson, Stephen K. [5 ]
Ewy, Rodger [1 ]
Singh, Sukhvinder [1 ]
Nguyen, Hoang [1 ]
McLaren, Paul J. [7 ,8 ]
Viard, Mathias [5 ]
Naranbhai, Vivek [2 ,3 ]
Zou, Chengcheng [9 ]
Lin, Zhansong [9 ]
Gatanaga, Hiroyuki [9 ,10 ]
Oka, Shinichi [9 ,10 ]
Takiguchi, Masafumi [9 ]
Thio, Chloe L. [11 ]
Margolick, Joseph [12 ]
Kirk, Gregory D. [13 ]
Goedert, James J. [14 ]
Hoots, W. Keith [15 ]
Deeks, Steven G. [16 ]
Haas, David W. [17 ]
Michael, Nelson [18 ]
Walker, Bruce [2 ,3 ,19 ,20 ]
Le Gall, Sylvie [2 ,3 ]
Chowdhury, Fatema Z. [2 ,3 ]
Yu, Xu G. [2 ,3 ]
Carrington, Mary [2 ,3 ,5 ]
机构
[1] Texas Biomed Res Inst, San Antonio, TX 78227 USA
[2] MIT, Massachusetts Gen Hosp, Ragon Inst, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[3] Harvard Univ, Cambridge, MA 02138 USA
[4] Olink Prote, Watertown, MA USA
[5] Frederick Natl Lab Canc Res, Basic Sci Program, Frederick, MD 21701 USA
[6] NCI, Canc & Inflammat Program, Ctr Canc Res, NIH, Frederick, MD 21701 USA
[7] Publ Hlth Agcy Canada, JC Wilt Infect Dis Res Ctr, Winnipeg, MB, Canada
[8] Univ Manitoba, Dept Med Microbiol & Infect Dis, Winnipeg, MB, Canada
[9] Kumamoto Univ, Ctr AIDS Res, Kumamoto, Japan
[10] Natl Ctr Global Hlth & Med, AIDS Clin Ctr, Tokyo, Japan
[11] Johns Hopkins Univ, Dept Med, Baltimore, MD USA
[12] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Dept Mol Microbiol & Immunol, Baltimore, MD USA
[13] Johns Hopkins Univ, Dept Epidemiol, Baltimore, MD USA
[14] NCI, Epidemiol & Biostat Program, Div Canc Epidemiol & Genet, Rockville, MD USA
[15] NHLBI, Div Blood Dis & Resources, NIH, Bldg 10, Bethesda, MD 20892 USA
[16] San Francisco Gen Hosp, Med Ctr, San Francisco, CA 94110 USA
[17] Vanderbilt Univ, Sch Med, Nashville, TN 37212 USA
[18] Walter Reed Army Inst Res, US Mil HIV Res Program, Silver Spring, MD USA
[19] Howard Hughes Med Inst, Chevy Chase, MD USA
[20] MIT, Inst Med Engn & Sci, 77 Massachusetts Ave, Cambridge, MA 02139 USA
关键词
LONG NONCODING RNAS; HOST GENETIC-VARIATION; MESSENGER-RNA; VIRUS REPLICATION; EXPRESSION; INFECTION; PROGRESSION; CELLS; HEPATITIS; DENSITY;
D O I
10.1038/s41590-019-0406-1
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Multiple genome-wide studies have identified associations between outcome of human immunodeficiency virus (HIV) infection and polymorphisms in and around the gene encoding the HIV co-receptor CCR5, but the functional basis for the strongest of these associations, rs1015164A/G, is unknown. We found that rs1015164 marks variation in an activating transcription factor 1 binding site that controls expression of the antisense long noncoding RNA (lncRNA) CCR5AS. Knockdown or enhancement of CCR5AS expression resulted in a corresponding change in CCR5 expression on CD4(+) Tcells. CCR5AS interfered with interactions between the RNA-binding protein Raly and the CCR5 3' untranslated region, protecting CCR5 messenger RNA from Raly-mediated degradation. Reduction in CCR5 expression through inhibition of CCR5AS diminished infection of CD4(+) Tcells with CCR5-tropic HIV in vitro. These data represent a rare determination of the functional importance of a genome-wide disease association where expression of a lncRNA affects HIV infection and disease progression.
引用
收藏
页码:824 / +
页数:13
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