Document Detail


Biogenesis of intronic miRNAs located in clusters by independent transcription and alternative splicing.
MedLine Citation:
PMID:  24226766     Owner:  NLM     Status:  Publisher    
Abstract/OtherAbstract:
miRNAs are generally classified as "intergenic" or "intronic" based upon their genomic location. Intergenic miRNAs are known to be transcribed as independent transcription units, while intronic miRNAs are believed to be processed from the introns of their hosting transcription units and hence share common regulatory mechanisms and expression patterns with its host gene. Recent reports in the literature suggest that some intronic miRNAs, which do not show concordance in expression with their respective host genes, might be transcribed and regulated as independent transcription units. However, there is no direct evidence for the existence of independently transcribed intronic miRNA in humans to date. We have characterized the full-length primary transcripts (pri-miRNAs) of three human intronic miRNAs-miR 106b, miR 93, and miR 24-1-by RNA ligase-mediated RACE and show that human intronic miRNA can indeed be transcribed as independent transcription units. Also, clustered miRNAs are generally believed to arise from a common primary transcript and are expected to have similar expression profiles. However, we have identified several novel alternatively spliced transcripts by RT-PCR, each of which harbors a single pre-miRNA from a cluster of closely located intronic miRNAs. We show that these transcripts represent unique pri-miRNAs for each of these clustered miRNAs. We also report the identification of conserved splice acceptor signals which are responsible for maturation of these novel splice variants. Our results suggest that alternative splicing might play a role in uncoupling the expression of clustered miRNAs from each other, which otherwise are generally believed to be co-transcribed and co-expressed.
Authors:
Pradeep Ramalingam; Jayanth Kumar Palanichamy; Anand Singh; Prerna Das; Mohita Bhagat; Muzaffer Ahmad Kassab; Subrata Sinha; Parthaprasad Chattopadhyay
Related Documents :
7537266 - The c-jun proto-oncogene down-regulates the rat alpha-fetoprotein promoter in hepg2 hep...
9545246 - Rb binds c-jun and activates transcription.
25341426 - E2f1 induces mir-224/452 expression to drive emt through txnip downregulation.
1906606 - The ap-1 site is required for basal expression but is not necessary for tpa-response of...
20738326 - Matrix metalloproteinase-2 regulates the expression of tissue inhibitor of matrix metal...
25152886 - A bayesian framework that integrates heterogeneous data for inferring gene regulatory n...
Publication Detail:
Type:  JOURNAL ARTICLE     Date:  2013-11-13
Journal Detail:
Title:  RNA (New York, N.Y.)     Volume:  -     ISSN:  1469-9001     ISO Abbreviation:  RNA     Publication Date:  2013 Nov 
Date Detail:
Created Date:  2013-11-14     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  9509184     Medline TA:  RNA     Country:  -    
Other Details:
Languages:  ENG     Pagination:  -     Citation Subset:  -    
Affiliation:
Department of Biochemistry, All India Institute of Medical Sciences, New Delhi 110029, India.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Adherence to the Mediterranean diet and risk of bladder cancer in the EPIC cohort study.
Next Document:  Themis sets the signal threshold for positive and negative selection in T-cell development.