scholarly journals Interactome analysis and docking sites prediction of (AtCHR8, AtCUL4 and AtERCC1/UVR7) proteins in Arabidopsis Thaliana

2020 ◽  
Vol 2 (1) ◽  
pp. 52-68
Author(s):  
Mohamed Ragab Abdel Gawwad ◽  
Ali Taha Ozdemir

The UV irradiation is a major DNA damaging factor in plants. Arabidopsis thaliana uses various repair pathways for these kinds of DNA lesions. One of them is the nucleotide excision repair pathway. The AtCUL4, ERCC1/UVR7 and CHR8 are vital proteins for nucleotide excision pathway and mutations in these proteins cause flaws in the repair mechanism. Two of these proteins play crucial role during DNA damage recognition and the other is involved in the excision of damaged bases. During NER processes, Arabidopsis uses different sets of proteins during the DNA damage recognition for transcriptionally active and genomic DNA. In order to get better insight into these proteins, we used bioinformatics tools to predict, analyze, and validate 3D structures of ERCC1/UVR7, AtCUL4 and CHR8. We also predicted the subcellular and sub-nuclear localization of proteins. Subsequently, we predicted the docking sites for each individual proteins and searched for interacting residues which mediate the protein-protein interactions. 

2020 ◽  
Vol 11 (1) ◽  
Author(s):  
Cristina Ribeiro-Silva ◽  
Mariangela Sabatella ◽  
Angela Helfricht ◽  
Jurgen A. Marteijn ◽  
Arjan F. Theil ◽  
...  

Abstract DNA damage sensors DDB2 and XPC initiate global genome nucleotide excision repair (NER) to protect DNA from mutagenesis caused by helix-distorting lesions. XPC recognizes helical distortions by binding to unpaired ssDNA opposite DNA lesions. DDB2 binds to UV-induced lesions directly and facilitates efficient recognition by XPC. We show that not only lesion-binding but also timely DDB2 dissociation is required for DNA damage handover to XPC and swift progression of the multistep repair reaction. DNA-binding-induced DDB2 ubiquitylation and ensuing degradation regulate its homeostasis to prevent excessive lesion (re)binding. Additionally, damage handover from DDB2 to XPC coincides with the arrival of the TFIIH complex, which further promotes DDB2 dissociation and formation of a stable XPC-TFIIH damage verification complex. Our results reveal a reciprocal coordination between DNA damage recognition and verification within NER and illustrate that timely repair factor dissociation is vital for correct spatiotemporal control of a multistep repair process.


Biochemistry ◽  
2004 ◽  
Vol 43 (21) ◽  
pp. 6832-6832
Author(s):  
Yue Zou ◽  
Huaxian Ma ◽  
Irina G. Minko ◽  
Steven M. Shell ◽  
Zhengguan Yang ◽  
...  

2019 ◽  
Vol 41 (1) ◽  
Author(s):  
Masayuki Kusakabe ◽  
Yuki Onishi ◽  
Haruto Tada ◽  
Fumika Kurihara ◽  
Kanako Kusao ◽  
...  

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