Target Name: RNU2-1
NCBI ID: G6066
Review Report on RNU2-1 Target / Biomarker Content of Review Report on RNU2-1 Target / Biomarker
RNU2-1
Other Name(s): RNA, U2 small nuclear 1 | U2 | RNU2

RNA Molecule in Regulating Protein Translation, Gene Expression, DNA Replication and Repair

RNA, U2 small nuclear 1 (RNLU2-1), is a non-coding RNA molecule that has been shown to play a critical role in various cellular processes. One of its key functions is to help regulate the translation of RNA into protein, which is a critical step in the development and maintenance of cellular structures and functions.

RNLU2-1 is a small RNA molecule, with only about 180 amino acid residues. It is made up of a single exon that is located within the U2 RNA domain of the small nuclear RNA (snRNA) family. U2 snRNAs are a class of RNA molecules that are highly conserved across various species and are involved in a variety of cellular processes, including the regulation of gene expression, DNA replication, and repair, and the control of RNA stability.

One of the unique features of RNLU2-1 is its ability to interact with other molecules, including proteins and nucleic acids. This interaction is critical for its function in regulating the translation of RNA into protein.

RNLU2-1 has been shown to interact with several proteins, including the protein encoded by the U2 gene, which is located on chromosome 9. The interaction between RNLU2-1 and U2 protein has been shown to play a role in regulating the translation of RNA into protein and in the process of protein synthesis.

In addition to its role in protein synthesis, RNLU2-1 has also been shown to play a critical role in regulating gene expression. This is because of its ability to interact with the RNA polymerase II (RNA polymerase II) complex, which is responsible for transcribing DNA into RNA.

RNLU2-1 has been shown to interact with RNA polymerase II in a variety of cellular contexts. For example, studies have shown that RNLU2-1 can interact with RNA polymerase II in the cytoplasm of cells and that this interaction is critical for the translation of RNA into protein.

Furthermore, RNLU2-1 has also been shown to play a role in regulating DNA replication and repair. This is because of its ability to interact with the DNA-binding protein encoded by the DNMT1 gene, which is located on chromosome 18.

RNLU2-1 has been shown to interact with DNA-binding protein encoded by the DNMT1 gene in a variety of cellular contexts. For example, studies have shown that RNLU2-1 can interact with DNA-binding protein encoded by the DNMT1 gene in the nucleus of cells and that this interaction is critical for the regulation of DNA replication and repair.

In conclusion, RNLU2-1 is a non-coding RNA molecule that plays a critical role in various cellular processes, including the regulation of gene expression, DNA replication, and repair, and the control of RNA stability. Its ability to interact with other molecules, including proteins and nucleic acids, makes it an attractive drug target and a potential biomarker for a variety of diseases. Further research is needed to fully understand the role of RNLU2-1 in cellular processes and to develop effective therapies based on its properties.

Protein Name: RNA, U2 Small Nuclear 1

The "RNU2-1 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 RNU2-1 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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