Regulation of the Apolipoprotein Gene Cluster by a Long Noncoding RNA

被引:178
作者
Halley, Paul [1 ,2 ]
Kadakkuzha, Beena M. [1 ,2 ]
Faghihi, Mohammad Ali [1 ,2 ]
Magistri, Marco [1 ,2 ]
Zeier, Zane [1 ,2 ]
Khorkova, Olga [3 ]
Coito, Carlos [3 ]
Hsiao, Jane [3 ]
Lawrence, Matthew [4 ]
Wahlestedt, Claes [1 ,2 ]
机构
[1] Univ Miami, Miller Sch Med, Ctr Therapeut Innovat, Miami, FL 33136 USA
[2] Univ Miami, Miller Sch Med, Dept Psychiat & Behav Sci, Miami, FL 33136 USA
[3] OPKO CURNA, Miramar, FL 33025 USA
[4] RxGen Inc, Hamden, CT 06517 USA
来源
CELL REPORTS | 2014年 / 6卷 / 01期
关键词
NATURAL ANTISENSE TRANSCRIPTS; MESSENGER-RNA; DRUG TARGETS; HUMAN GENOME; CHROMATIN; CELLS; LIPOPROTEINS; EXPRESSION; DISEASE; LSD1;
D O I
10.1016/j.celrep.2013.12.015
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Apolipoprotein A1 (APOA1) is the major protein component of high-density lipoprotein (HDL) in plasma. We have identified an endogenously expressed long noncoding natural antisense transcript, APOA1-AS, which acts as a negative transcriptional regulator of APOA1 both in vitro and in vivo. Inhibition of APOA1-AS in cultured cells resulted in the increased expression of APOA1 and two neighboring genes in the APO cluster. Chromatin immunoprecipitation (ChIP) analyses of a similar to 50 kb chromatin region flanking the APOA1 gene demonstrated that APOA1-AS can modulate distinct histone methylation patterns that mark active and/or inactive gene expression through the recruitment of histone-modifying enzymes. Targeting APOA1-AS with short antisense oligonucleotides also enhanced APOA1 expression in both human and monkey liver cells and induced an increase in hepatic RNA and protein expression in African green monkeys. Furthermore, the results presented here highlight the significant local modulatory effects of long noncoding antisense RNAs and demonstrate the therapeutic potential of manipulating the expression of these transcripts both in vitro and in vivo.
引用
收藏
页码:222 / 230
页数:9
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