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| Status |
Public on Mar 01, 2020 |
| Title |
Codon and amino acid content regulate mRNA stability in mammalian cells |
| Organisms |
Homo sapiens; Cricetulus griseus |
| Experiment type |
Expression profiling by high throughput sequencing
Non-coding RNA profiling by high throughput sequencing
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| Summary |
mRNA degradation is a critical aspect of gene expression which dictates mRNA steady-state levels in conjunction with transcription rate. Previous studies in other model organisms have demonstrated that enrichment of specific codons within the open reading frame (ORF) can influence mRNA stability, primarily by modulating translation elongation speed. Despite advancements in our understanding of mRNA stability regulation by microRNAs and 3'UTR-based factors in mammalian systems, the importance of other mRNA regions such as the ORF sequence on dictating cellular mRNA levels are incompletely understood. To characterize the effects of the coding sequence on mRNA decay in mammals, we analyzed mRNA stability in human and Chinese Hamster Ovary (Cricetulus griseus) cells by both global metabolic labeling and single-gene mRNA reporter transcription shutoffs. In agreement with previous studies, we observed that synonymous codon usage impacts mRNA stability in mammalian cells. Unexpectedly, we also found that amino acid content is a potent determinant of mRNA stability in humans and other mammalian species. Codon and amino acid effects on decay correlate with tRNA levels measured by tRNA-Seq or intracellular amino acid levels measured by HPLC, respectively. These results suggest that both tRNA and amino acid levels have complementary effects on regulation of mRNA stability in mammals, hinting at the possibility of dynamic control of mRNA levels via altered tRNA or amino acid levels.
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| Overall design |
Metabolic labeling followed by RNA-seq of 10 time points to determine mRNA half lives in Chinese hamster ovary cells. In addition, tRNA sequencing replicates to determine tRNA levels in HeLa cells.
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| Contributor(s) |
Forrest ME, Pinkard O, Martin S, Sweet TJ, Arango D, Hanson G, Oberdoerffer S, Coller J |
| Citation(s) |
32053646 |
| |
| Submission date |
Oct 02, 2019 |
| Last update date |
Mar 02, 2020 |
| Contact name |
Jeff Coller |
| E-mail(s) |
jmc71@case.edu
|
| Phone |
216-368-0299
|
| Organization name |
Case Western Reserve University
|
| Department |
Center for RNA Science and Therapeutics
|
| Street address |
10900 Euclid Ave
|
| City |
Cleveland |
| State/province |
OH |
| ZIP/Postal code |
44106 |
| Country |
USA |
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| Platforms (2) |
| GPL20904 |
Illumina HiSeq 2500 (Cricetulus griseus) |
| GPL21697 |
NextSeq 550 (Homo sapiens) |
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| Samples (14)
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| Relations |
| BioProject |
PRJNA575354 |
| SRA |
SRP223940 |
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