共 50 条
OKseqHMM: a genome-wide replication fork directionality analysis toolkit
被引:8
作者:
Liu, Yaqun
[1
]
Wu, Xia
[1
]
d'Aubenton-Carafa, Yves
[2
]
Thermes, Claude
[2
]
Chen, Chun-Long
[1
,3
]
机构:
[1] Univ PSL, Sorbonne Univ, Inst Curie, CNRS UMR3244, F-75005 Paris, France
[2] Univ Paris Saclay, Inst Integrat Biol Cell I2BC, CEA, CNRS, F-91198 Gif Sur Yvette, France
[3] Sun Yat Sen Univ, Zhongshan Sch Med, Guangzhou 510080, Guangdong, Peoples R China
关键词:
DNA-REPLICATION;
PATTERNS;
DAMAGE;
D O I:
10.1093/nar/gkac1239
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
During each cell division, tens of thousands of DNA replication origins are co-ordinately activated to ensure the complete duplication of the human genome. However, replication fork progression can be challenged by many factors, including co-directional and head-on transcription-replication conflicts (TRC). Head-on TRCs are more dangerous for genome in-tegrity. To study the direction of replication fork movement and TRCs, we developed a bioinformatics toolkit called OKseqHMM (https://github.com/CL-CHEN-Lab/OK-Seq, https://doi.org/10.5281/zenodo. 7428883). Then, we used OKseqHMM to analyse a large number of datasets obtained by Okazaki fragment sequencing to directly measure the genome-wide replication fork directionality (RFD) and to accurately predict replication initiation and termination at a fine resolution in organisms including yeast, mouse and human. We also successfully applied our analysis to other genome-wide sequencing techniques that also contain RFD information (e.g. eS-PAN, TrAEL-seq). Our toolkit can be used to predict replication initiation and fork progression direction genome-wide in a wide range of cell models and growth conditions. Comparing the replication and transcription directions allows identifying loci at risk of TRCs, particularly head-on TRCs, and investigating their role in genome instability by checking DNA damage data, which is of prime importance for human health.
引用
收藏
页数:14
相关论文