Synapsis of DNA ends by DNA-dependent protein kinase.

EMBO J

Departments of Medicine and Biochemistry, Stanford University, Stanford, CA 94305, USA.

Published: June 2002

The catalytic subunit of DNA-dependent protein kinase (DNA-PK(CS)) is required for a non-homologous end-joining pathway that repairs DNA double-strand breaks produced by ionizing radiation or V(D)J recombination; however, its role in this pathway has remained obscure. Using a neutravidin pull-down assay, we found that DNA-PK(CS) mediates formation of a synaptic complex containing two DNA molecules. Furthermore, kinase activity was cooperative with respect to DNA concentration, suggesting that activation of the kinase occurs only after DNA synapsis. Electron microscopy revealed complexes of two DNA ends brought together by two DNA-PK(CS) molecules. Our results suggest that DNA-PK(CS) brings DNA ends together and then undergoes activation of its kinase, presumably to regulate subsequent steps for processing and ligation of the ends.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC126055PMC
http://dx.doi.org/10.1093/emboj/cdf299DOI Listing

Publication Analysis

Top Keywords

dna ends
12
dna-dependent protein
8
protein kinase
8
activation kinase
8
dna
6
kinase
5
synapsis dna
4
ends
4
ends dna-dependent
4
kinase catalytic
4

Similar Publications

Single-molecule techniques in studying the molecular mechanisms of DNA synapsis in non-homologous end-joining repair.

Biophys Rep

February 2025

Institute of Molecular and Translational Medicine (IMTM), and Department of Biochemistry and Molecular Biology, Xi'an Jiaotong University Health Science Center, Xi'an 710061, China.

DNA double-strand breaks (DSBs) are the most severe form of DNA damage, primarily repaired by the non-homologous end joining (NHEJ) pathway. A critical step in this process is DNA synapsis, where the two broken ends are brought together to facilitate timely repair. Deficiencies in NHEJ synapsis can lead to improper DNA end configurations, potentially resulting in chromosomal translocations.

View Article and Find Full Text PDF

Recruitment and rejoining of remote double-strand DNA breaks for enhanced and precise chromosome editing.

Genome Biol

March 2025

Gene Editing Center, School of Life Science and Technology, ShanghaiTech University, 393 Middle Huaxia Road, Pudong, Shanghai, 201210, China.

Chromosomal rearrangements, such as translocations, deletions, and inversions, underlie numerous genetic diseases and cancers, yet precise engineering of these rearrangements remains challenging. Here, we present a CRISPR-based homologous recombination-mediated rearrangement (HRMR) strategy that leverages homologous donor templates to align and repair broken chromosome ends. HRMR improves efficiency by approximately 80-fold compared to non-homologous end joining, achieving over 95% homologous recombination.

View Article and Find Full Text PDF

First record of watermelon crinkle leaf-associated virus 2 infecting watermelon in open field in Italy.

Plant Dis

March 2025

Istituto per la Protezione Sostenibile delle Piante del CNR, Via Università 133, Portici (NA), Italy, 80055;

Watermelon (Citrullus lanatus L.) is an important horticultural crop in Italy, with a production of around 600,000 tons per year (third producer in the Europe). Viruses are considered a limiting factor in watermelon production, especially those transmitted by efficient vectors such as whiteflies and aphids.

View Article and Find Full Text PDF

A terminator is a DNA region that ends the transcription process. Currently, multiple computational tools are available for predicting bacterial terminators. However, these methods are specialized for certain bacteria or terminator type (i.

View Article and Find Full Text PDF

Eukaryotes have linear DNA and their telomeres are hotspots for transposons, which in some cases took over telomere maintenance. Here we identify several families of independently evolved telomeric transposons in linear chromosomes and plasmids of cyanobacteria and . While these elements have one specific transposon end sequence, with the second boundary being the telomere, we can show that they move using two transposon ends, likely when transiently bridged by the telomere maintenance systems.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!