Related Experiment Video
Updated: Apr 28, 2026

10:25
Using the E1A Minigene Tool to Study mRNA Splicing Changes
Published on: April 22, 2021
4.5K
A new look at adenovirus splicing.
Hongxing Zhao1, Maoshan Chen1, Ulf Pettersson1
1Department of Immunology, Genetics and Immunology, Uppsala University, S-751 85 Uppsala, Sweden.
Virology
|June 4, 2014
Summary
Deep sequencing of Adenovirus type 2 RNA revealed novel splicing events and accurately mapped polyadenylation sites. This study corrects previous mapping errors and identifies new potential protein-coding or non-coding RNAs.
Area of Science:
- Molecular Biology
- Virology
- Genomics
Background:
- Adenovirus type 2 utilizes complex RNA splicing for gene expression.
- Previous mapping of splicing events had inconsistencies.
Purpose of the Study:
- To quantitatively map Adenovirus type 2 RNA splicing events.
- To accurately identify mRNA polyadenylation sites.
- To discover novel RNA species and assess their conservation.
Main Methods:
- Deep cDNA sequencing of Adenovirus type 2 RNA.
- Quantitative analysis of splice sites.
- Mapping of mRNA polyadenylation sites.
Main Results:
- Majority of previously identified splice sites were confirmed.
- Several previously mapped splice sites were corrected.
- New splice sites were identified, potentially coding for novel proteins or alternatively spliced mRNAs.
- Novel RNAs in the major late transcription unit showed high conservation.
- Adenovirus mRNA polyadenylation sites were accurately mapped and found to be heterogeneous.
Conclusions:
- Deep sequencing provides a more accurate map of Adenovirus type 2 RNA splicing.
- Novel RNA species identified warrant further investigation for their function.
- Accurate mapping of polyadenylation sites contributes to understanding Adenovirus gene regulation.
Related Concept Videos
Leaky Scanning
4.5K
During most eukaryotic translation processes, the small 40S ribosome subunit scans an mRNA from its 5' end until it encounters the first start AUG codon. The large 60S ribosomal subunit then joins the smaller one to initiate protein synthesis. The location of the translation initiation is largely determined by the nucleotides near the start codon as there may be multiple translation initiation sites present on the mRNA. Marilyn Kozak discovered that the sequence RCCAUGG (where R...
4.5K
RNA Splicing
53.3K
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...
53.3K
RNA Splicing
15.9K
15.9K
Pre-mRNA Processing: RNA Splicing
5.6K
5.6K
Alternative RNA Splicing
4.2K
4.2K
Alternative RNA Splicing
20.4K
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...
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...
20.4K

