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Engineered mischarged transfer RNAs for correcting pathogenic missense mutations [mRNA-seq]

ABSTRACT: Engineered mischarged transfer RNAs for correcting pathogenic missense mutations [mRNA-seq]

PROVIDER: PRJNA991919 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR25181400_1.fastq.gz	Fastqsanger.gz
	SRR25181400_2.fastq.gz	Fastqsanger.gz
	SRR25181401_1.fastq.gz	Fastqsanger.gz
	SRR25181401_2.fastq.gz	Fastqsanger.gz
	SRR25181402_1.fastq.gz	Fastqsanger.gz

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Engineered mischarged transfer RNAs for correcting pathogenic missense mutations

Project description:Engineered mischarged transfer RNAs for correcting pathogenic missense mutations

| PRJNA991914 | ENA

Engineered mischarged transfer RNAs for correcting pathogenic missense mutations [MSR-seq]

Project description:Missense mutations account for nearly 50% of pathogenic mutations in human genetic diseases, most lack effective treatments. Gene therapies, CRISPR-based gene editing, and RNA therapies including transfer RNA (tRNA) modalities are common strategies for potential treatments of genetic diseases. However, reported tRNA therapies are for nonsense mutations, how tRNAs can be engineered to correct missense mutations have not been explored. Here, we describe missense correcting tRNAs (mc-tRNAs) as a potential therapeutic modality for correcting pathogenic missense mutations. Mc-tRNAs are engineered tRNAs that are charged with one amino acid and read codons of another amino acid in translation in human cells. We first developed a series of fluorescence protein (FP)-based reporters that indicate successful correction of missense mutations via restoration of fluorescence signals. We engineered mc-tRNAs that effectively corrected Serine and Arginine missense mutations in the reporters and confirmed the amino acid substitution by protein mass spectrometry and mc-tRNA expression by tRNA sequencing. We examined the transcriptome response to the expression of mc-tRNAs and found some mc-tRNAs induced minimum transcriptomic changes. Furthermore, we applied an Arg-tRNAGln(CUG) mc-tRNA to rescue the autolytic activity of a pathogenic CAPN3 Arg-to-Gln mutant involved in limb-girdle muscular dystrophy type 2A. These results establish a versatile pipeline for mc-tRNA engineering and demonstrate the potential of mc-tRNA as an alternative therapeutic platform for the treatment of genetic disorders.

2024-01-04 | GSE236623 | GEO

Engineered mischarged transfer RNAs for correcting pathogenic missense mutations [mRNA-seq]

2024-01-04 | GSE236622 | GEO

Engineered mischarged transfer RNAs for correcting pathogenic missense mutations [MSR-seq]

Project description:Engineered mischarged transfer RNAs for correcting pathogenic missense mutations [MSR-seq]

| PRJNA991918 | ENA

Engineered mischarged transfer RNAs for correcting pathogenic missense mutations

Project description:This SuperSeries is composed of the SubSeries listed below.

2024-01-03 | GSE236624 | GEO

Ribosome profiling of selenoproteins in vivo reveals consequences of pathogenic Secisbp2 missense mutations

Project description:Re-coding of UGA codons as selenocysteine (Sec) codons in selenoproteins depends on a selenocysteine insertion sequence (SECIS) in the 3’ UTR of mRNAs of eukaryotic selenoproteins. SECIS-binding protein 2 (SECISBP2) increases the efficiency of this process. Pathogenic mutations in SECISBP2 reduce selenoprotein expression and lead to phenotypes associated with the reduction of deiodinase activities and selenoprotein N expression in humans. Two functions have been ascribed to SECISBP2: binding of SECIS elements in selenoprotein mRNAs and facilitation of co-translational Sec insertion. To separately probe both functions, we established here two mouse models carrying two pathogenic missense mutations in Secisbp2 previously identified in patients. We found that the C696R substitution in the RNAbinding domain abrogates SECIS binding and does not support selenoprotein translation above the level of a complete Secisbp2 null mutation. The R543Q missense substitution located in the selenocysteine insertion domain resulted in residual activity and caused reduced selenoprotein translation, as demonstrated by ribosomal profiling to determine the impact on UGA re-coding in individual selenoproteins. We found, however, that the R543Q variant is thermally unstable in vitro and completely degraded in the mouse liver in vivo, while being partially functional in the brain. The moderate impairment of selenoprotein expression in neurons led to astrogliosis and transcriptional induction of genes associated with immune responses. We conclude that differential SECISBP2 protein stability in individual cell types may dictate clinical phenotypes to a much greater extent than molecular interactions involving a mutated amino acid in SECISBP2 .

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Engineered cell elongation promotes extracellular electron transfer of Shewanella oneidensis

Project description:Engineered cell elongation promotes extracellular electron transfer of Shewanella oneidensis

| PRJNA1022018 | ENA

rare HER2 missense mutations promote the oncogenic signaling and migration of breast cancer

Project description:Proteomic and phosphoproteomic data for rare HER2 missense mutations

2023-03-20 | PXD040988 |

Effect of Network-Correcting Molecules

Project description:Effect of Network-Correcting Molecules

| PRJNA635425 | ENA

The complex etiology of autism spectrum disorder due to missense mutations of CHD8

Project description:CHD8 is an ATP-dependent chromatin-remodeling factor encoded by the most frequently mutated gene in individuals with autism spectrum disorder (ASD). Although many studies have examined the consequences of CHD8 haploinsufficiency in cells and mice, few have focused on missense mutations, the most common type of CHD8 alteration in ASD patients. We here characterized CHD8 missense mutations in ASD patients according to six prediction scores and experimentally examined the effects of such mutations on the biochemical activities of CHD8, neural differentiation of embryonic stem cells, and mouse behavior. Only mutations with high prediction scores gave rise to ASD-like phenotypes in mice, suggesting that not all CHD8 missense mutations detected in ASD patients are directly responsible for the development of ASD. Furthermore, we found that mutations with high scores cause ASD by mechanisms either dependent on or independent of loss of chromatin-remodeling function. Our results thus provide insight into the molecular underpinnings of ASD pathogenesis caused by missense mutations of CHD8.

2024-02-28 | GSE227579 | GEO

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