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Structure and activity of putative intronic miRNA promoters
被引:289
作者:
Monteys, Alex Mas
[1
]
Spengler, Ryan M.
[1
]
Wan, Ji
[2
]
Tecedor, Luis
[1
]
Lennox, Kimberly A.
[3
]
Xing, Yi
[2
]
Davidson, Beverly L.
[1
,4
,5
]
机构:
[1] Univ Iowa, Dept Internal Med, Iowa City, IA 52242 USA
[2] Univ Iowa, Dept Biomed Engn, Iowa City, IA 52242 USA
[3] Integrated DNA Technol, Coralville, IA 52246 USA
[4] Univ Iowa, Dept Mol Physiol & Biophys, Iowa City, IA 52242 USA
[5] Univ Iowa, Dept Neurol, Iowa City, IA 52242 USA
来源:
关键词:
Pol II;
Pol III;
intronic;
microRNA promoters;
RNA-POLYMERASE-III;
ACUTE LYMPHOBLASTIC-LEUKEMIA;
MICRORNA TRANSCRIPTS;
NUCLEOTIDE-SEQUENCES;
NUCLEAR EXPORT;
IN-VITRO;
EXPRESSION;
GENES;
DROSOPHILA;
PROTEIN;
D O I:
10.1261/rna.1731910
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:
MicroRNAs (miRNAs) are RNA sequences of similar to 22 nucleotides that mediate post-transcriptional regulation of specific mRNAs. miRNA sequences are dispersed throughout the genome and are classified as intergenic (between genes) or intronic (embedded into a gene). Intergenic miRNAs are expressed by their own promoter, and until recently, it was supposed that intronic miRNAs are transcribed from their host gene. Here, we performed a genomic analysis of currently known intronic miRNA regions and observed that similar to 35% of intronic miRNAs have upstream regulatory elements consistent with promoter function. Among all intronic miRNAs, 30% have associated Pol II regulatory elements, including transcription start sites, CpG islands, expression sequence tags, and conserved transcription factor binding sites, while 5% contain RNA Pol III regulatory elements (A/B box sequences). We cloned intronic regions encompassing miRNAs and their upstream Pol II (miR-107, miR-126, miR-208b, miR548f-2, miR-569, and miR-590) or Pol III (miR-566 and miR-128-2) sequences into a promoterless plasmid, and confirmed that miRNA expression occurs independent of host gene transcription. For miR-128-2, a miRNA overexpressed in acute lymphoblastic leukemia, ChIP analysis suggests dual regulation by both intronic (Pol III) and host gene (Pol II) promoters. These data support complex regulation of intronic miRNA expression, and have relevance to disregulation in disease settings.
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页码:495 / 505
页数:11
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