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Related Concept Videos

RNA Splicing01:32

RNA Splicing

Splicing is the process by which eukaryotic RNA is edited before its translation into protein. The RNA strand transcribed from eukaryotic DNA is called the primary transcript. The primary transcripts that become mRNAs are called precursor messenger RNAs (pre-mRNAs). Eukaryotic pre-mRNA contains alternating sequences of exons and introns. Exons are nucleotide sequences that code for proteins, whereas introns are the non-coding regions. In RNA splicing, introns are removed and exons are bonded...
Alternative RNA Splicing02:18

Alternative RNA Splicing

Alternative RNA splicing is the regulated splicing of exons and introns to produce different mature mRNAs from a single pre-mRNA. Unlike in constitutive splicing where a single gene produces a single type of mRNA, alternative splicing allows an organism to produce multiple proteins from a single gene and plays an important role in protein diversity.
There are five types of alternative RNA splicing that vary in the ways the pre-mRNA segments are removed or retained in the mature mRNA. The first...
Exon Recombination02:32

Exon Recombination

The evolution of new genes is critical for speciation. Exon recombination, also known as exon shuffling or domain shuffling, is an important means of new gene formation. It is observed across vertebrates, invertebrates, and in some plants such as potatoes and sunflowers. During exon recombination, exons from the same or different genes recombine and produce new exon-intron combinations, which might evolve into new genes. 
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RNA-seq03:21

RNA-seq

RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases. 
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Single Nucleotide Polymorphisms-SNPs01:05

Single Nucleotide Polymorphisms-SNPs

A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
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Cell Signaling in Plants

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Related Experiment Video

Updated: Jul 28, 2026

Annotation of Plant Gene Function via Combined Genomics, Metabolomics and Informatics
08:09

Annotation of Plant Gene Function via Combined Genomics, Metabolomics and Informatics

Published on: June 17, 2012

Multiple snoRNA gene clusters from Arabidopsis.

J W Brown1, G P Clark, D J Leader

  • 1Unit of Gene Expression, Genetics Division, Scottish Crop Research Institute, Dundee, United Kingdom. lowe@soe.ucsc.edu

RNA (New York, N.Y.)
|January 10, 2002
PubMed
Summary

Small nucleolar RNAs (snoRNAs) in plants are commonly organized in polycistronic clusters, with many novel genes and methylation sites discovered. This organization differs from vertebrates and highlights snoRNA evolution in plants.

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Area of Science:

  • Molecular Biology
  • Genetics
  • Plant Science

Background:

  • Small nucleolar RNAs (snoRNAs) are crucial for ribosomal RNA (rRNA) processing and modification.
  • Gene organization for snoRNAs varies across eukaryotes, with vertebrates primarily using intronic encoding, while maize and yeast utilize polycistronic transcripts.

Purpose of the Study:

  • To identify and characterize small nucleolar RNA (snoRNA) gene clusters and novel snoRNA genes in plants.
  • To map 2'-O-ribose methylation sites in plant ribosomal RNAs (rRNAs).
  • To investigate the gene organization and evolutionary mechanisms of snoRNAs in plants.

Main Methods:

  • Bioinformatic searches and gene cloning were used to identify snoRNA gene copies and clusters.
  • Primer extension analysis was employed to map 2'-O-ribose methylation sites in plant rRNAs.
  • Isolation and characterization of specific snoRNA gene clusters from Arabidopsis.

Main Results:

  • Identified 43 snoRNA gene clusters, 1 intronic snoRNA, and 10 single genes, totaling 136 copies of 71 different snoRNAs, with 31 novel to plants.
  • Characterized Arabidopsis snoRNA clusters, including novel box C/D (snoR4) and box H/ACA (snoR5) genes.
  • Mapped 42 putative 2'-O-ribose methylation sites in plant rRNAs, with eight sites novel to plants.

Conclusions:

  • The predominant snoRNA gene organization in plants is polycistronic.
  • A significant portion of predicted and mapped methylation sites in plant rRNAs are novel.
  • Variations in gene cluster organization suggest diverse mechanisms driving snoRNA evolution in plants.