DNA polymerase lambda

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DNA polymerase lambda (Pol λ) is a DNA polymerase enzyme found in eukaryotes, including humans. It is involved in DNA repair and V(D)J recombination, playing a critical role in maintaining the integrity of the genome. Pol λ belongs to the X family of DNA polymerases, which also includes Pol β and TdT.

Function[edit | edit source]

DNA polymerase lambda is versatile, participating in various DNA repair pathways, notably base excision repair (BER) and non-homologous end joining (NHEJ). In BER, Pol λ can fill in the gaps left after damaged bases are removed. During NHEJ, which repairs double-strand breaks, Pol λ can add nucleotides to the DNA ends, facilitating their rejoining.

Structure[edit | edit source]

The enzyme consists of several domains: a polymerase domain, which synthesizes new DNA strands; a BRCT domain, involved in protein-protein interactions; and a proline-rich domain, which may interact with other components of the DNA repair machinery. The structure of Pol λ allows it to interact with both DNA and other proteins involved in repair processes, enhancing its efficiency and versatility in DNA repair.

Clinical Significance[edit | edit source]

Mutations in the POLλ gene can lead to genomic instability and contribute to the development of cancer. Given its role in DNA repair, Pol λ is also a potential target for cancer therapy. Inhibitors of Pol λ could sensitize cancer cells to DNA-damaging agents, making it a promising avenue for research.

Evolution[edit | edit source]

Pol λ is evolutionarily conserved across eukaryotes, indicating its essential role in DNA repair. Comparative studies of Pol λ and other X family polymerases have provided insights into the mechanisms of DNA repair and the evolution of the DNA replication machinery.

Research[edit | edit source]

Research on DNA polymerase lambda continues to uncover its mechanisms of action, regulation, and interaction with other proteins in the cell. Understanding Pol λ's function in DNA repair pathways is crucial for elucidating the molecular basis of genomic stability and the development of novel therapeutic strategies targeting DNA repair in cancer.

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Contributors: Prab R. Tumpati, MD