Related Experiment Video
Updated: Jun 20, 2026

10:21
Cell Based Assays of SINEUP Non-coding RNAs That Can Specifically Enhance mRNA Translation
Published on: February 1, 2019
Posttranslational interference of Ty1 retrotransposition by antisense RNAs
Emiko Matsuda1, David J Garfinkel
1Gene Regulation and Chromosome Biology Laboratory, Center for Cancer Research, National Cancer Institute, Frederick, MD 21702-1201, USA.
Summary
Antisense RNAs from the Ty1 retrotransposon in Saccharomyces cerevisiae limit its movement. These RNAs reduce key proteins, preventing Ty1 replication and integration, offering insight into transposon control.
Area of Science:
- Molecular Biology
- Genetics
- Genomics
Background:
- Transposable elements (TEs) can disrupt genome integrity and gene expression.
- RNA interference (RNAi) is a common mechanism for TE control, but not universally conserved.
- Saccharomyces cerevisiae lacks canonical RNAi pathways, necessitating alternative TE suppression strategies.
Purpose of the Study:
- To investigate the mechanisms by which Saccharomyces cerevisiae controls retrotransposon movement.
- To determine the role of antisense (AS) RNAs from the Ty1 element in regulating its own retrotransposition.
Main Methods:
- Analysis of Ty1 antisense RNA (Ty1AS) transcripts and their overlap with Ty1 copy number control (CNC) regions.
- Experimental manipulation of Ty1 copy number and CNC region sequences.
- Assessment of Ty1AS RNA levels, protein expression (integrase, reverse transcriptase), and cDNA synthesis.
- Localization studies of Ty1AS RNAs within virus-like particles.
Main Results:
- Multiple Ty1AS transcripts were identified, overlapping with essential Ty1 CNC sequences.
- Ty1AS RNAs were found to inhibit Ty1 transposition in trans.
- Changes in Ty1 copy number or CNC region integrity affected Ty1AS RNA levels and transposition.
- Ty1AS RNAs correlated with reduced integrase and reverse transcriptase levels and impaired Ty1 cDNA synthesis.
Conclusions:
- Antisense RNAs (Ty1AS) represent an intrinsic mechanism for limiting Ty1 retrotransposition in Saccharomyces cerevisiae.
- Ty1AS RNAs act post-translationally by decreasing the abundance of proteins required for Ty1 replication and integration.
- This study reveals a novel non-RNAi pathway for transposon control in yeast.
Related Concept Videos
Non-LTR Retrotransposons
As the name suggests, non-LTR retrotransposons lack the long terminal repeats characteristic of the LTR retrotransposons. Additionally, both LTR and non-LTR retrotransposons use distinct mechanisms of mobilization. Non-LTR retrotransposons are further divided into two classes - Long interspersed nuclear elements (LINEs) and short interspersed nuclear elements (SINEs), both of which occur abundantly in most mammals, including humans. Some of the active non-LTR retrotransposons in humans are L1...
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...
LTR Retrotransposons
LTR retrotransposons are class I transposable elements with long terminal repeats flanking an internal coding region. These elements are less abundant in mammals compared to other class I transposable elements. About 8 percent of human genomic DNA comprises LTR retrotransposons. Some of the common examples of LTR retrotransposons are Ty elements in yeast and Copia elements in Drosophila.
The internal coding region of LTR retrotransposons and their mechanism of transposition closely resembles a...
The internal coding region of LTR retrotransposons and their mechanism of transposition closely resembles a...
siRNA - Small Interfering RNAs
Small interfering RNAs, or siRNAs, are short regulatory RNA molecules that can silence genes post-transcriptionally, as well as the transcriptional levelĀ in some cases. siRNAs are important for protecting cells against viral infections and silencing transposable genetic elements.
In the cytoplasm, siRNA is processed from a double-stranded RNA, which comes from either endogenous DNA transcription or exogenous sources like a virus. This double-stranded RNA is then cleaved by the ATP-dependent...
In the cytoplasm, siRNA is processed from a double-stranded RNA, which comes from either endogenous DNA transcription or exogenous sources like a virus. This double-stranded RNA is then cleaved by the ATP-dependent...
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...
RNA Interference
RNA interference (RNAi) is a process in which a small non-coding RNA molecule blocks the post-transcriptional expression of a gene by binding to its messenger RNA (mRNA) and preventing the protein from being translated.
This process occurs naturally in cells, often through the activity of genomically-encoded microRNAs. Researchers can take advantage of this mechanism by introducing synthetic RNAs to deactivate specific genes for research or therapeutic purposes. For example, RNAi could be used...
This process occurs naturally in cells, often through the activity of genomically-encoded microRNAs. Researchers can take advantage of this mechanism by introducing synthetic RNAs to deactivate specific genes for research or therapeutic purposes. For example, RNAi could be used...

