Target Name: POLM
NCBI ID: G27434
Review Report on POLM Target / Biomarker Content of Review Report on POLM Target / Biomarker
POLM
Other Name(s): DNA-directed DNA/RNA polymerase mu | Tdt-N | Terminal transferase | terminal transferase | DNA-directed DNA/RNA polymerase mu (isoform 1) | DNA polymerase mu, transcript variant 1 | POLM variant 1 | DNA polymerase mu | polymerase (DNA-directed), mu | DPOLM_HUMAN | Polymerase (DNA-directed), mu | Pol Mu | Pol iota | FLJ35482 | polymerase (DNA) mu

Mutations in The POLM Gene Linked To A Range of Diseases

POLM, or DNA-directed DNA/RNA polymerase mu, is a enzyme that plays a crucial role in the process of DNA replication and gene expression. Mutations in the POLM gene have been linked to a range of diseases, including cancer, neurodegenerative diseases, and inherited disorders. As a result, POLM has emerged as a promising drug target and a biomarker for a variety of diseases.

The POLM gene is a member of the polymerase I (DNA-directed DNA polymerase) family, which includes enzymes that participate in the replication of DNA in eukaryotic cells. These enzymes use a unique mechanism of action, in which a single template strand of DNA is used to synthesize a new complementary strand. This allows for efficient and precise replication of the genetic material.

Mutations in the POLM gene can have a significant impact on the function of the enzyme. Studies have shown that POLM mutations can lead to a range of changes in the enzyme's activity and stability. For example, some mutations can alter the Polm enzyme's catalytic rate, while others can affect the stability of the enzyme. These changes can have important implications for the function of the enzyme and its role in disease.

One of the most significant consequences of POLM mutations is their ability to alter the expression of target genes. This is because the Polm enzyme is involved in the regulation of a wide range of gene expression factors, including those that control cell growth, apoptosis, and inflammation. As a result, any changes in the Polm enzyme's activity or stability can have a profound impact on the expression of nearby genes.

This is particularly important for understanding the mechanisms of many diseases, including cancer. Many mutations in cancer-causing genes have been shown to alter the function of the Polm enzyme. For example, mutations in the BRCA gene, which encodes a protein that plays a role in regulating the replication of cancer-causing DNA, have been linked to increased risk of breast and ovarian cancer. Similarly, mutations in the PIK3CA gene, which encodes a protein that regulates cell growth and survival, have been linked to the development of many types of cancer.

In addition to its role in cancer, Polm mutations have also been linked to a range of other diseases, including neurodegenerative diseases and inherited disorders. For example, mutations in the POLM gene have been linked to the development of a range of neurodegenerative diseases, including Alzheimer's disease, Parkinson's disease, and Huntington's disease. Similarly, mutations in the gene have also been linked to a range of inherited disorders, including sickle cell disease and thalassemia.

Given the importance of Polm mutations for the regulation of gene expression and the development of many diseases, there is a growing interest in using Polm as a drug target or biomarker. This is because targeting the Polm enzyme has the potential to disrupt the mechanisms of many diseases and provide new treatments.

One approach to targeting Polm as a drug is through the use of small molecules that inhibit the activity of the Polm enzyme. These small molecules can be designed to interact with specific regions of the Polm enzyme and disrupt its activity. This can lead to a range of potential benefits, including the inhibition of cancer growth and the treatment of neurodegenerative diseases.

Another approach to targeting Polm is through the use of genetic modifiers that alter the expression of the Polm gene. These genetic modifiers can include drugs that regulate the activity of the Polm enzyme, such as small molecules that enhance the activity of the enzyme, or changes to the Polm gene that alter its stability. For example, researchers have

Protein Name: DNA Polymerase Mu

Functions: Gap-filling polymerase involved in repair of DNA double-strand breaks by non-homologous end joining (NHEJ). Participates in immunoglobulin (Ig) light chain gene rearrangement in V(D)J recombination

The "POLM 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 POLM 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

POLN | POLQ | POLR1A | POLR1B | POLR1C | POLR1D | POLR1E | POLR1F | POLR1G | POLR1H | POLR1HASP | POLR2A | POLR2B | POLR2C | POLR2D | POLR2E | POLR2F | POLR2G | POLR2H | POLR2I | POLR2J | POLR2J2 | POLR2J3 | POLR2J4 | POLR2K | POLR2L | POLR2LP1 | POLR2M | POLR3A | POLR3B | POLR3C | POLR3D | POLR3E | POLR3F | POLR3G | POLR3GL | POLR3H | POLR3K | POLRMT | POLRMTP1 | Poly [ADP-ribose] polymerase | Polycomb Repressive Complex 1 (PRC1) | Polycomb Repressive Complex 2 | POM121 | POM121B | POM121C | POM121L12 | POM121L15P | POM121L1P | POM121L2 | POM121L4P | POM121L7P | POM121L8P | POM121L9P | POMC | POMGNT1 | POMGNT2 | POMK | POMP | POMT1 | POMT2 | POMZP3 | PON1 | PON2 | PON3 | POP1 | POP4 | POP5 | POP7 | POPDC2 | POPDC3 | POR | PORCN | POSTN | POT1 | POT1-AS1 | Potassium Channels | POTEA | POTEB | POTEB2 | POTEB3 | POTEC | POTED | POTEE | POTEF | POTEG | POTEH | POTEI | POTEJ | POTEKP | POTEM | POU-Domain transcription factors | POU1F1 | POU2AF1 | POU2AF2 | POU2AF3 | POU2F1 | POU2F2 | POU2F3 | POU3F1