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Related Concept Videos

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. 
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while microarray-based...
Ribosomal RNA Synthesis02:53

Ribosomal RNA Synthesis

Ribosome synthesis is a highly complex and coordinated process involving more than 200 assembly factors. The synthesis and processing of ribosomal components occurs not only in the nucleolus but also in the nucleoplasm and the cytoplasm of eukaryotic cells.
Ribosome biogenesis begins with the synthesis of 5S and 45S pre-rRNAs by distinct RNA polymerases. The primary transcripts are extensively processed and modified before they are bound and folded by ribosomal proteins and assembly factors,...
Ribosomal RNA Synthesis02:53

Ribosomal RNA Synthesis

Ribosome synthesis is a highly complex and coordinated process involving more than 200 assembly factors. The synthesis and processing of ribosomal components occurs not only in the nucleolus but also in the nucleoplasm and the cytoplasm of eukaryotic cells.
Ribosome biogenesis begins with the synthesis of 5S and 45S pre-rRNAs by distinct RNA polymerases. The primary transcripts are extensively processed and modified before they are bound and folded by ribosomal proteins and assembly factors,...
Bacterial RNA Polymerase00:43

Bacterial RNA Polymerase

Unlike eukaryotes, bacteria use a single RNA Polymerase (RNAP) to transcribe all genes. The different subunits of bacterial RNAPhave distinct functions. The multisubunit structure of the bacterial RNAP helps the enzyme to maintain catalytic function, facilitate assembly, interact with DNA and RNA, and self-regulate its activity.
In most genes, the transcription site is a single base present upstream of the coding sequence. Though RNAP is a catalytically efficient enzyme, it does not recognize...
RNA Structure01:23

RNA Structure

Overview
The basic structure of RNA consists of a five-carbon sugar and one of four nitrogenous bases. Although most RNA is single-stranded, it can form complex secondary and tertiary structures. Such structures play essential roles in the regulation of transcription and translation.
Different Types of RNA Have the Same Basic Structure
There are three main types of ribonucleic acid (RNA): messenger RNA (mRNA), transfer RNA (tRNA), and ribosomal RNA (rRNA). All three RNA types consist of a...
RNA Structure01:19

RNA Structure

The basic structure of RNA consists of a string of ribonucleotides attached by phosphodiester bonds. Although most RNA is single-stranded, it can form complex secondary and tertiary structures. Such structures play essential roles in the regulation of transcription and translation.
Different Types of RNA Have the Same Basic Structure
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Related Experiment Video

Updated: Jun 27, 2026

Global Identification of Co-Translational Interaction Networks by Selective Ribosome Profiling
06:58

Global Identification of Co-Translational Interaction Networks by Selective Ribosome Profiling

Published on: October 7, 2021

5.8S-28S rRNA interaction and HMM-based ITS2 annotation.

Alexander Keller1, Tina Schleicher, Jörg Schultz

  • 1Department of Bioinformatics, University of Würzburg, Biocenter, Am Hubland, 97074 Würzburg, Germany.

Gene
|November 26, 2008
PubMed
Summary

Accurate delimitation of the internal transcribed spacer 2 (ITS2) is crucial for phylogenetic analysis. This study introduces a new hidden Markov model (HMM) tool to precisely identify and delineate ITS2 sequences, improving phylogenetic study reliability.

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The ITS2 Database
16:17

The ITS2 Database

Published on: March 12, 2012

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Last Updated: Jun 27, 2026

Global Identification of Co-Translational Interaction Networks by Selective Ribosome Profiling
06:58

Global Identification of Co-Translational Interaction Networks by Selective Ribosome Profiling

Published on: October 7, 2021

The ITS2 Database
16:17

The ITS2 Database

Published on: March 12, 2012

Area of Science:

  • Molecular Biology
  • Bioinformatics
  • Phylogenetics

Background:

  • The internal transcribed spacer 2 (ITS2) is a widely used phylogenetic marker due to its evolutionary rate and conserved secondary structure.
  • Inconsistent annotation of ITS2 start and end positions hinders accurate secondary structure prediction and phylogenetic analyses.
  • Correct ITS2 delineation is essential for reliable secondary structure modeling and multiple sequence alignments.

Purpose of the Study:

  • To develop and validate a novel tool for accurate ITS2 sequence delimitation and identification.
  • To address the shortcomings of existing methods in annotating ITS2 boundaries.
  • To provide a reliable method for the crucial initial step in ITS2-based phylogenetic studies.

Main Methods:

  • Utilized hidden Markov models (HMMs) for ITS2 identification and delimitation.
  • Verified annotations by comparing with conserved structural motifs in 5.8S/28S rRNA regions.
  • Applied the method to large datasets from GenBank and ITS2-DB for re-annotation.

Main Results:

  • Successfully identified and delimited ITS2 in over 30,000 unannotated GenBank entries.
  • Re-annotated approximately 45,000 questionable ITS2 sequences and 30,000 from ITS2-DB.
  • Demonstrated accurate annotation of ITS2 sequences ranging from 58 nt (Giardia lamblia) to 1160 nt (humans).

Conclusions:

  • The developed HMM-based tool provides accurate and reliable ITS2 delineation.
  • This method significantly improves the accuracy of phylogenetic analyses relying on ITS2 markers.
  • The tool is a valuable resource for researchers conducting molecular evolution and biodiversity studies.