Target Name: CWC25
NCBI ID: G54883
Review Report on CWC25 Target / Biomarker Content of Review Report on CWC25 Target / Biomarker
CWC25
Other Name(s): Pre-mRNA-splicing factor CWC25 homolog | CWC25 variant 1 | Spliceosome-associated protein homolog CWC25 | CWC25 spliceosome associated protein homolog, transcript variant 1 | CWC25 spliceosome associated protein homolog | coiled-coil domain-containing protein 49 | Coiled-coil domain-containing protein 49 | CWC25_HUMAN | CCDC49 | FLJ20291

CWC25: A Potential Drug Target and Biomarker for Splice-Error-Induced Cellular Stress

Splice errors are a common event in gene expression, which can lead to the production of aberrant RNA species that can have adverse effects on the cell. The pre-mRNA-splicing factor CWC25 homolog (CSPF-like 25) is a non-coding RNA molecule that has been shown to play a critical role in the regulation of splicing efficiency. In this article, we discuss the potential implications of CWC25 as a drug target and biomarker for cellular stress caused by splicing errors.

CWC25 Homolog: Structure and Function

The CWC25 homolog is a member of the CWC25 family, which is characterized by the presence of a single exon and a single splice enhancer domain. The splice enhancer domain is responsible for binding to the splicing machinery and enhancing the expression of target genes.

The CWC25 homolog is expressed in various tissues and cells, including brain, heart, and muscle. It has been shown to play a role in the regulation of splicing efficiency, as well as the expression of target genes.

CWC25 Homolog as a Potential Drug Target

The CWC25 homolog is a promising drug target due to its involvement in cellular stress caused by splicing errors. Splice errors can lead to the production of aberrant RNA species, which can cause cellular stress and contribute to the development of various diseases, including cancer.

One of the key mechanisms by which CWC25 homolog contributes to cellular stress is its role in the regulation of splicing efficiency. Splice errors can lead to the production of RNA species that are not functional, which can cause the cell to enter a state of stress. The CWC25 homolog has been shown to play a role in the regulation of splicing efficiency, which may help to prevent the accumulation of aberrant RNA species and reduce cellular stress.

Another potential mechanism by which CWC25 homolog contributes to cellular stress is its role in the regulation of gene expression. The CWC25 homolog has been shown to play a role in the regulation of the expression of target genes, which may help to ensure that cells are able to withstand the challenges posed by splicing errors.

CWC25 Homolog as a Biomarker

The CWC25 homolog has also been shown to be a potential biomarker for cellular stress caused by splicing errors. Splice errors can lead to the production of aberrant RNA species that are not functional, which can cause cellular stress and contribute to the development of various diseases. The CWC25 homolog has been shown to be involved in the regulation of splicing efficiency, which may help to prevent the accumulation of aberrant RNA species and reduce cellular stress.

Conclusion

The CWC25 homolog is a non-coding RNA molecule that has been shown to play a critical role in the regulation of splicing efficiency. Its involvement in the regulation of splicing efficiency and gene expression makes it a promising drug target and biomarker for cellular stress caused by splicing errors. Further research is needed to fully understand the mechanisms by which CWC25 homolog contributes to cellular stress and to develop effective treatments for splicing errors-induced diseases.

Protein Name: CWC25 Spliceosome Associated Protein Homolog

Functions: Involved in pre-mRNA splicing as component of the spliceosome

The "CWC25 Target / Biomarker Review Report" is a customizable review of hundreds up to thousends of related scientific research literature by AI technology, covering specific information about CWC25 comprehensively, including but not limited to:
•   general information;
•   protein structure and compound binding;
•   protein biological mechanisms;
•   its importance;
•   the target screening and validation;
•   expression level;
•   disease relevance;
•   drug resistance;
•   related combination drugs;
•   pharmacochemistry experiments;
•   related patent analysis;
•   advantages and risks of development, etc.
The report is helpful for project application, drug molecule design, research progress updates, publication of research papers, patent applications, etc. If you are interested to get a full version of this report, please feel free to contact us at BD@silexon.ai

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