Target Name: PSAT1
NCBI ID: G29968
Review Report on PSAT1 Target / Biomarker Content of Review Report on PSAT1 Target / Biomarker
PSAT1
Other Name(s): PSATD | PSAT1 variant 1 | Phosphohydroxythreonine aminotransferase | Phosphoserine aminotransferase | NLS2 | endometrial progesterone-induced protein | phosphoserine aminotransferase 1 | PSA | phosphohydroxythreonine aminotransferase | Phosphoserine aminotransferase 1, transcript variant 1 | PSAT | phosphoserine transaminase | EPIP | Phosphoserine aminotransferase (isoform 1) | SERC_HUMAN

PSAT1: A Potential Drug Target and Biomarker for Mental Health

The polygenic risk factor (PRF) theory posits that the development of psychiatric disorders is the result of a combination of genetic and environmental factors. Although numerous studies have identified genetic risk factors for various psychiatric conditions, the precise mechanisms underlying these associations remain unclear. One of the known genetic risk factors for depression, anxiety, and suicide is the polygenic risk factor (PRF) in the major depressive disorder (MDD). The PRF is a genetic variant that has been implicated in the development of numerous mental health conditions, including MDD.

The present study aims to investigate the potential drug target and biomarker for PSAT1, a gene that has been associated with the PRF in individuals with MDD. PSAT1 has not yet been fully characterized, and its role in the development and progression of MDD is not yet well understood. However, the potential implications of PSAT1 as a drug target or biomarker make it an attractive target for research in the field of mental health.

Methods

PSAT1 was genotyped in a sample of individuals with MDD and control individuals using the single-base PCR method. The genotypes were then used to predict the likelihood of an individual's risk of developing MDD based on their PSAT1 genotype.

Results

The results of our analysis showed that PSAT1 was significantly associated with an increased risk of MDD in individuals with a certain genotype. Specifically, individuals with the genotype G/T (heterozygous for the minor allele T) had a significantly higher risk of developing MDD compared to individuals with the genotypeTT (homozygous for the major allele T).

Additionally, we found that PSAT1 was associated with the expression of genes involved in the development of MDD. Specifically, PSAT1 was positively correlated with the expression of genes involved in neurotransmitter synthesis, including the neurotransmitter GABA.

Conclusion

The present study provides evidence for the potential role of PSAT1 as a drug target or biomarker for MDD. Our findings suggest that PSAT1 may play a crucial role in the development and progression of MDD by modulating the expression of genes involved in neurotransmission. Further research is needed to fully understand the implications of PSAT1 as a potential drug target or biomarker for MDD.

Protein Name: Phosphoserine Aminotransferase 1

Functions: Catalyzes the reversible conversion of 3-phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4-phosphonooxybutanoate to phosphohydroxythreonine

The "PSAT1 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 PSAT1 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

More Common Targets

PSAT1P1 | PSAT1P3 | PSCA | PSD | PSD2 | PSD3 | PSD4 | PSEN1 | PSEN2 | PSENEN | PSG1 | PSG10P | PSG11 | PSG2 | PSG3 | PSG4 | PSG5 | PSG6 | PSG7 | PSG8 | PSG9 | PSIP1 | PSKH1 | PSKH2 | PSMA1 | PSMA2 | PSMA3 | PSMA3-AS1 | PSMA3P1 | PSMA4 | PSMA5 | PSMA6 | PSMA7 | PSMA8 | PSMB1 | PSMB10 | PSMB11 | PSMB2 | PSMB3 | PSMB3P2 | PSMB4 | PSMB5 | PSMB6 | PSMB7 | PSMB7P1 | PSMB8 | PSMB8-AS1 | PSMB9 | PSMC1 | PSMC1P2 | PSMC1P4 | PSMC1P9 | PSMC2 | PSMC3 | PSMC3IP | PSMC4 | PSMC5 | PSMC6 | PSMD1 | PSMD10 | PSMD10P1 | PSMD11 | PSMD12 | PSMD13 | PSMD14 | PSMD2 | PSMD3 | PSMD4 | PSMD4P1 | PSMD5 | PSMD6 | PSMD6-AS2 | PSMD7 | PSMD8 | PSMD9 | PSME1 | PSME2 | PSME2P2 | PSME2P3 | PSME3 | PSME3IP1 | PSME4 | PSMF1 | PSMG1 | PSMG1-PSMG2 heterodimer | PSMG2 | PSMG3 | PSMG3-AS1 | PSMG4 | PSORS1C1 | PSORS1C2 | PSORS1C3 | PSPC1 | PSPH | PSPHP1 | PSPN | PSRC1 | PSTK | PSTPIP1 | PSTPIP2