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Related Concept Videos

Cis-regulatory Sequences02:02

Cis-regulatory Sequences

Cis-regulatory sequences are short fragments of non-coding DNA that are present on the same chromosomes as the genes that they regulate. These fragments serve as binding sites for transcriptional regulators, proteins that are responsible for controlling gene transcription and differential gene expression across cell types in eukaryotes. Cis-regulatory sequences can be close to the gene of interest or thousands of bases away in the DNA sequence; however, those sequences that are further away are...
Cis-regulatory Sequences02:02

Cis-regulatory Sequences

Cis-regulatory sequences are short fragments of non-coding DNA that are present on the same chromosomes as the genes that they regulate. These fragments serve as binding sites for transcriptional regulators, proteins that are responsible for controlling gene transcription and differential gene expression across cell types in eukaryotes. Cis-regulatory sequences can be close to the gene of interest or thousands of bases away in the DNA sequence; however, those sequences that are further away are...
piRNA - Piwi-interacting RNAs02:57

piRNA - Piwi-interacting RNAs

PIWI-interacting RNAs, or piRNAs, are the most abundant short non-coding RNAs. More than 20,000 genes have been found in humans that code for piRNAs while only 2000 genes have been found for miRNAs. piRNAs can act at the transcriptional and post-transcriptional levels and have a vital role in silencing transposable elements present in germ cells. They are also involved in epigenetic silencing and activation. Previously, they were thought to function only in germ cells but new evidence suggests...
Multi-species Conserved Sequences02:51

Multi-species Conserved Sequences

Next-generation sequencing technologies have created large genomic databases of a variety of animals and plants. Ever since the human genome project was completed, scientists studied the genome of primates, mammals, and other phylogenetically distant living beings. Such large-scaleĀ  studies have provided new insights into the evolutionary relationship between organisms.
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Experimental RNAi02:15

Experimental RNAi

RNA interference (RNAi) is a cellular mechanism that inhibits gene expression by suppressing its transcription or activating the RNA degradation process. The mechanism was discovered by Andrew Fire and Craig Mello in 1998 in plants. Today, it is observed in almost all eukaryotes, including protozoa, flies, nematodes, insects, parasites, and mammals. This precise cellular mechanism of gene silencing has been developed into a technique that provides an efficient way to identify and determine the...
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...

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mirMachine: A One-Stop Shop for Plant miRNA Annotation
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mirMachine: A One-Stop Shop for Plant miRNA Annotation

Published on: May 1, 2021

CpG Islands as a putative source for animal miRNAs: evolutionary and functional implications.

Dvir Dahary1, Reut Shalgi, Yitzhak Pilpel

  • 1Department of Molecular Genetics, Weizmann Institute of Science, Rehovot, Israel.

Molecular Biology and Evolution
|November 25, 2010
PubMed
Summary

Novel microRNA (miR) families, crucial for animal evolution, originate from distinct genomic sources: transposable elements and CpG islands. This study reveals their unique evolutionary paths and characteristics, clarifying miR origins in regulatory networks.

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Published on: August 21, 2019

Area of Science:

  • Evolutionary biology
  • Genomics
  • Molecular biology

Background:

  • MicroRNAs (miRs) are key regulators in animal development and evolution.
  • The evolutionary origins of novel miR families remain largely unknown.
  • Understanding miR origins is crucial for deciphering animal morphological complexity.

Purpose of the Study:

  • To investigate the genomic origins of novel microRNA families.
  • To explore two potential sources: transposable elements and CpG islands.
  • To differentiate the evolutionary trajectories and characteristics of miRs from these distinct origins.

Main Methods:

  • Comparative genomics analysis.
  • Phylogenetic analysis of miR families.
  • Characterization of functional and genomic features of miRs.

Main Results:

  • Identified transposable elements and CpG islands as distinct sources for novel miR families.
  • Demonstrated that miRs from these two origins exhibit significantly different genomic and functional characteristics.
  • Showcased that these origins are evolutionarily independent.

Conclusions:

  • Provides evidence for dual genomic origins of novel miR families in animals.
  • Highlights the distinct evolutionary pathways and functional implications of miRs from different genomic sources.
  • Offers insights into the evolution of gene regulatory networks.