APOBEC · Enzymatic DNA deamination and the immunity/cancer balance
Horizon 2020 — Marie Skłodowska-Curie Actions
- Duration
- 2015-04-01 → 2017-03-31
- EU contribution
- €159,461
- Participants
- 1
- Scheme
- MSCA-IF
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Results in brief
Enzymatic DNA deamination and the immunity/cancer balance
The problem originally addressed in the project in the frame of the Marie Curie program related to the role of the APOBEC family of DNA deaminating enzymes in the generation of somatic antibody diversity, control of viral infection and lymphomagenesis. All these issues are central for human health and disease and therefore of great importance for society. The original objectives of the proposal were to 1) determine the contribution of APOBEC3 catalytic activity to genomic instability 2) understand the mechanism of kataegis (a special category of extensive localized mutagenesis) and the regulation of human APOBEC enzymes 3) delineate the requirement for aberrant AID activity in inflammation-associated carcinogenesis.
Data: CORDIS, © European Union
Project objective
Genomic instability is a key hallmark of cancer. Chromosome translocations require the formation of pairs of double-strand breaks (DSB) and trans-chromosomal ligation of the broken ends. Members of the AID/APOBEC family of enzymes deaminate cytosine (C) to uracil (U) in the context of a polynucleotide substrate. Excision of the U residue from DNA produces an abasic site, leading to incision of the DNA strand containing the abasic site by the conventional base-excision repair pathway. The introduction of proximal incisions on both DNA strands can generate a DSB intermediate for chromosomal translocation. AID acts on C residues at immunoglobulin loci in activated B cells to trigger antibody gene diversification and is the only member of the AID/APOBEC family that is currently known to act physiologically on endogenous nuclear DNA. Off-target deamination by AID results in nucleotide substitutions and genomic rearrangements in B lymphocyte tumours. APOBEC1 edits mRNA transcripts in the small intestine. Liver-directed misexpression of APOBEC1 is oncogenic in transgenic mice. APOBEC3 enzymes are ubiquitously expressed and act on C residues in the cDNA viral replication intermediates as part of a host restriction pathway. APOBEC3A and APOBEC3B have been shown to be capable of causing genomic damage in mammalian cells. Access to the nucleus by APOBEC family members likely permits DNA deamination activity that introduces mutations and genomic instability during tumourigenesis. I have generated mice that harbour FLAG-tagged forms of AID, APOBEC1, APOBEC3A or APOBEC3B inserted at the ROSA26 locus, preceded by a floxed stop sequence for conditional expression. This system will be used to understand the role of cytosine deamination in tumour progression in tissue- and time-specific contexts in vivo through whole genome sequencing of tumours. The long-term goal is to initiate the development of reagents to regulate APOBEC activity in basic science and clinical oncology.
Original text from CORDIS.
Participants
- MAX DELBRUECK CENTRUM FUER MOLEKULARE MEDIZIN IN DER HELMHOLTZ-GEMEINSCHAFT (MDC) · BerlinCoordinatorGermany
Links
- View on CORDIS
- DOI: 10.3030/660883
- http://web.archive.org/web/20171105064748/https://www.mdc-berlin.de/research-report-2016
Data: CORDIS, © European Union