Abstract |
Analysis of translocation breakpoints in human B cell malignancies reveals that DNA double-strand breaks at oncogenes most frequently occur at CpG sites located within 20-600 bp fragile zones and depend on activation-induced deaminase (AID). AID requires single-stranded DNA (ssDNA) to act, but it has been unclear why or how this region transiently acquires a ssDNA state. Here, we demonstrate the ssDNA state in the 23 bp E2A fragile zone using several methods, including native bisulfite DNA structural analysis in live human pre-B cells. AID deamination within the E2A fragile zone does not require but is increased upon transcription. High C-string density, nascent RNA tails, and direct DNA sequence repeats prolong the ssDNA state of the E2A fragile zone and increase AID deamination at overlapping AID hotspots that contain the CpG sites at which breaks occur in patients. These features provide key insights into lymphoid fragile zones generally.
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Authors | Di Liu, Yong-Hwee Eddie Loh, Chih-Lin Hsieh, Michael R Lieber |
Journal | Cell reports
(Cell Rep)
Vol. 36
Issue 2
Pg. 109387
(07 13 2021)
ISSN: 2211-1247 [Electronic] United States |
PMID | 34260910
(Publication Type: Journal Article, Research Support, N.I.H., Extramural)
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Copyright | Copyright © 2021 The Author(s). Published by Elsevier Inc. All rights reserved. |
Chemical References |
- Basic Helix-Loop-Helix Transcription Factors
- TCF3 protein, human
- Ribonuclease, Pancreatic
- Cytidine Deaminase
|
Topics |
- B-Lymphocytes
(immunology)
- Base Pairing
(genetics)
- Base Sequence
- Basic Helix-Loop-Helix Transcription Factors
(genetics)
- Chromosome Breakage
- Chromosomes, Human
(genetics)
- CpG Islands
(genetics)
- Cytidine Deaminase
- Deamination
- Humans
- Introns
(genetics)
- Lymphocytes
(metabolism)
- Neoplasms
(genetics, immunology)
- Ribonuclease, Pancreatic
(metabolism)
- Substrate Specificity
- Translocation, Genetic
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