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Related Concept Videos

MicroRNAs01:22

MicroRNAs

MicroRNA (miRNA) are short, regulatory RNA transcribed from introns (non-coding regions of a gene) or intergenic regions (stretches of DNA present between genes). Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself, forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After the pre-miRNA...
MicroRNAs01:22

MicroRNAs

MicroRNA (miRNA) are short, regulatory RNA transcribed from introns—non-coding regions of a gene—or intergenic regions—stretches of DNA present between genes. Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After the pre-miRNA ends...
MicroRNAs01:22

MicroRNAs

MicroRNA (miRNA) are short, regulatory RNA transcribed from introns—non-coding regions of a gene—or intergenic regions—stretches of DNA present between genes. Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After the pre-miRNA ends...
Ribosome Profiling02:24

Ribosome Profiling

Ribosome profiling or ribo-sequencing is a deep sequencing technique that produces a snapshot of active translation in a cell. It selectively sequences the mRNAs protected by ribosomes to get an insight into a cell’s translation landscape at any given point in time.
Applications of ribosome profiling
Ribosome profiling has many applications, including in vivo monitoring of translation inside a particular organ or tissue type and quantifying new protein synthesis levels.
The technique helps...

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CRISPR Gene Editing Tool for MicroRNA Cluster Network Analysis
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CRISPR Gene Editing Tool for MicroRNA Cluster Network Analysis

Published on: April 25, 2022

Genomic analysis of human microRNA transcripts.

Harpreet Kaur Saini1, Sam Griffiths-Jones, Anton James Enright

  • 1Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB10 1SA, United Kingdom.

Proceedings of the National Academy of Sciences of the United States of America
|October 30, 2007
PubMed
Summary

This study reveals the primary transcript structures for intergenic microRNAs (miRNAs), essential genetic regulators. Researchers identified distinct 3-4 kb transcripts with clear boundaries for these crucial non-coding RNAs.

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Identifying Targets of Human microRNAs with the LightSwitch Luciferase Assay System using 3'UTR-reporter Constructs and a microRNA Mimic in Adherent Cells
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Identifying Targets of Human microRNAs with the LightSwitch Luciferase Assay System using 3'UTR-reporter Constructs and a microRNA Mimic in Adherent Cells

Published on: September 28, 2011

Area of Science:

  • Genetics
  • Molecular Biology
  • Bioinformatics

Background:

  • MicroRNAs (miRNAs) are key genetic regulators involved in development, differentiation, growth, and metabolism.
  • While intronic miRNA transcription is understood, the primary transcript structure of intergenic miRNAs remains largely unknown.
  • The human genome encodes approximately 500 known miRNA genes, with about half originating from non-protein-coding transcripts.

Purpose of the Study:

  • To elucidate the primary transcript structure of intergenic miRNAs in the human genome.
  • To improve the understanding of the transcriptional regulation and organization of intergenic miRNAs.
  • To characterize the genomic features associated with intergenic miRNA primary transcripts.

Main Methods:

  • Large-scale analysis of genomic features including transcription start sites, polyadenylation signals, and CpG islands.
  • Integration of EST data, transcription factor-binding sites, and expression ditag data.
  • Bioinformatic analysis of intergenic miRNA loci in the human genome.

Main Results:

  • A significant fraction of intergenic miRNA primary transcripts were found to be 3-4 kb in length.
  • These transcripts exhibit clearly defined 5' and 3' boundaries.
  • Strong evidence was provided for the complete transcript structure of several human intergenic miRNAs.

Conclusions:

  • The study provides significant insights into the transcriptional units of intergenic miRNAs.
  • Identified transcript structures suggest independent transcriptional regulation for a subset of intergenic miRNAs.
  • This work lays the foundation for further functional studies of intergenic miRNAs and their regulatory networks.