Importance of Germline and Somatic Alterations in Human MRE11, RAD50, and NBN Genes Coding for MRN Complex
Jazyk angličtina Země Švýcarsko Médium electronic
Typ dokumentu časopisecké články, přehledy
Grantová podpora
NU22-03-00276
Ministry of Health
DRO-VFN-64165
Ministry of Health
COOPERATIO
Charles University
SVV260516
Charles University
EXCELES no. LX22NPO05102
Ministry of Education Youth and Sports
PubMed
36982687
PubMed Central
PMC10051278
DOI
10.3390/ijms24065612
PII: ijms24065612
Knihovny.cz E-zdroje
- Klíčová slova
- ATLD, DNA repair, MRE11, NBN, NBS, NBSLD, NGS, RAD50, TP53, hereditary cancer syndromes, variant interpretation,
- MeSH
- ATM protein genetika metabolismus MeSH
- DNA vazebné proteiny genetika metabolismus MeSH
- enzymy opravy DNA genetika metabolismus MeSH
- homologní protein MRE11 genetika metabolismus MeSH
- hydrolasy působící na anhydridy kyselin genetika metabolismus MeSH
- jaderné proteiny genetika metabolismus MeSH
- lidé MeSH
- nádorové supresorové proteiny * genetika MeSH
- oprava DNA genetika MeSH
- proteiny buněčného cyklu * metabolismus MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
- Názvy látek
- ATM protein MeSH
- DNA vazebné proteiny MeSH
- enzymy opravy DNA MeSH
- homologní protein MRE11 MeSH
- hydrolasy působící na anhydridy kyselin MeSH
- jaderné proteiny MeSH
- nádorové supresorové proteiny * MeSH
- NBN protein, human MeSH Prohlížeč
- proteiny buněčného cyklu * MeSH
- RAD50 protein, human MeSH Prohlížeč
The MRE11, RAD50, and NBN genes encode for the nuclear MRN protein complex, which senses the DNA double strand breaks and initiates the DNA repair. The MRN complex also participates in the activation of ATM kinase, which coordinates DNA repair with the p53-dependent cell cycle checkpoint arrest. Carriers of homozygous germline pathogenic variants in the MRN complex genes or compound heterozygotes develop phenotypically distinct rare autosomal recessive syndromes characterized by chromosomal instability and neurological symptoms. Heterozygous germline alterations in the MRN complex genes have been associated with a poorly-specified predisposition to various cancer types. Somatic alterations in the MRN complex genes may represent valuable predictive and prognostic biomarkers in cancer patients. MRN complex genes have been targeted in several next-generation sequencing panels for cancer and neurological disorders, but interpretation of the identified alterations is challenging due to the complexity of MRN complex function in the DNA damage response. In this review, we outline the structural characteristics of the MRE11, RAD50 and NBN proteins, the assembly and functions of the MRN complex from the perspective of clinical interpretation of germline and somatic alterations in the MRE11, RAD50 and NBN genes.
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