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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.
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页码:824 / +
页数:13
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