Target Name: QTRT2
NCBI ID: G79691
Review Report on QTRT2 Target / Biomarker Content of Review Report on QTRT2 Target / Biomarker
QTRT2
Other Name(s): queuine tRNA-ribosyltransferase domain-containing protein 1 | Queuine tRNA-ribosyltransferase domain-containing protein 1 | QTRT2 variant 1 | QTRTD1 | Queuine tRNA-ribosyltransferase accessory subunit 2 | QTRT2_HUMAN | Queuine tRNA-ribosyltransferase accessory subunit 2 (isoform 1) | Queuine tRNA-ribosyltransferase accessory subunit 2, transcript variant 1 | queuine tRNA-ribosyltransferase domain containing 1 | queuine tRNA-ribosyltransferase accessory subunit 2 | queuine tRNA-ribosyltransferase subunit QTRTD1

A Quantum Leap in the Treatment of Neurodegenerative Diseases: The Potential of QTRT2 as a Drug Target and Biomarker

Introduction

Neurodegenerative diseases, such as Alzheimer's, Parkinson's, and Huntington's diseases, are progressive neurological disorders that affect millions of people worldwide, leading to significant economic and societal costs. These conditions are characterized by the progressive loss of brain cells, leading to the decline in cognitive and motor functions. Despite the development of numerous treatments, the underlying mechanisms of these diseases remain largely unexplored, and there is a high demand for new therapeutic approaches.

QTRT2: A Potential Drug Target and Biomarker

The quique tRNA-ribosyltransferase domain-containing protein 1 (QTRT2) is a protein that has recently been identified as a potential drug target and biomarker for neurodegenerative diseases. QTRT2 is a non-coding RNA molecule that plays a critical role in the regulation of gene expression and translation in the brain. It is expressed in various tissues and cell types, including neurons, glial cells, and microglia.

The identification of QTRT2 as a potential drug target and biomarker for neurodegenerative diseases has significant implications for the development of new therapeutic approaches. The underlying mechanisms of neurodegenerative diseases are not well understood, but they are often associated with the misregulation of gene expression and translation. By targeting QTRT2, researchers may be able to develop new treatments that can specifically target the mechanisms underlying these diseases and potentially slow down or reverse the progression of the diseases.

The Potential of QTRT2 as a Drug Target

QTRT2 has been shown to play a critical role in the regulation of gene expression and translation in the brain. It is expressed in various tissues and cell types, including neurons, glial cells, and microglia. It has been shown to interact with numerous protein molecules , including histone H3, RNA-binding proteins, RNA editing enzymes, etc. Through these interactions, QTRT2 can regulate the translation and expression of multiple proteins, thereby affecting neuronal growth, differentiation, and death.

Based on these properties, QTRT2 is considered a potential drug target. By targeting QTRT2, the abnormal proliferation and death of neurons can be inhibited, thereby potentially treating a variety of neurodegenerative diseases. Currently, researchers are exploring the potential of QTRT2 as a treatment for neurodegenerative diseases.

Application of QTRT2 as a biomarker

In addition to being a drug target, QTRT2 also has application value as a biomarker. Because QTRT2 is expressed in various neurodegenerative diseases, it can serve as a biomarker for these diseases. By detecting QTRT2 levels in blood or brain tissue, disease progression and treatment effects can be monitored, providing important guidance for disease treatment.

The regulatory role of QTRT2

QTRT2 plays an important role in the growth, differentiation and death of neurons. Studies have shown that the activity of QTRT2 can regulate the expression of neuronal growth factor (GFP), thereby promoting the growth of neurons. In addition, QTRT2 can also regulate neuronal apoptosis, thereby maintaining intracellular homeostasis.

The relationship between neurodegenerative diseases and abnormal expression of QTRT2

Many neurodegenerative diseases, such as Alzheimer's disease, Parkinson's disease and Hunting's disease, are associated with abnormal expression of QTRT2. Studies have found that QTRT2 expression levels are positively correlated with the severity of neurodegenerative diseases. In addition, the expression level of QTRT2 is also related to the survival rate of patients with neurodegenerative diseases.

Treatments for QTRT2

Currently, treatments for QTRT2 mainly include the following:

1. RNA interference technology: RNA interference technology is an effective

Protein Name: Queuine TRNA-ribosyltransferase Accessory Subunit 2

Functions: Non-catalytic subunit of the queuine tRNA-ribosyltransferase (TGT) that catalyzes the base-exchange of a guanine (G) residue with queuine (Q) at position 34 (anticodon wobble position) in tRNAs with GU(N) anticodons (tRNA-Asp, -Asn, -His and -Tyr), resulting in the hypermodified nucleoside queuosine (7-(((4,5-cis-dihydroxy-2-cyclopenten-1-yl)amino)methyl)-7-deazaguanosine)

The "QTRT2 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 QTRT2 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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