IBB PAS Repository

Unique mechanism of target recognition by PfoI restriction endonuclease of the CCGG-family.

Tamulaitiene, Giedre and Manakova, Elena and Jovaisaite, Virginija and Tamulaitis, Gintautas and Grazulis, Saulius and Bochtler, Matthias and Siksnys, Virginijus (2019) Unique mechanism of target recognition by PfoI restriction endonuclease of the CCGG-family. Nucleic Acids Research, 47 (2). pp. 997-1010. ISSN 0305-1048

[img] PDF
3MB

Official URL: https://academic.oup.com/nar/article/47/2/997/5184...

Abstract

Restriction endonucleases (REs) of the CCGG-family recognize a set of 4-8 bp target sequences that share a common CCGG or CCNGG core and possess PD…D/ExK nuclease fold. REs that interact with 5 bp sequence 5'-CCNGG flip the central N nucleotides and 'compress' the bound DNA to stack the inner base pairs to mimic the CCGG sequence. PfoI belongs to the CCGG-family and cleaves the 7 bp sequence 5'-T|CCNGGA ("|" designates cleavage position). We present here crystal structures of PfoI in free and DNA-bound forms that show unique active site arrangement and mechanism of sequence recognition. Structures and mutagenesis indicate that PfoI features a permuted E…ExD…K active site that differs from the consensus motif characteristic to other family members. Although PfoI also flips the central N nucleotides of the target sequence it does not 'compress' the bound DNA. Instead, PfoI induces a drastic change in DNA backbone conformation that shortens the distance between scissile phosphates to match that in the unperturbed CCGG sequence. Our data demonstrate the diversity and versatility of structural mechanisms employed by restriction enzymes for recognition of related DNA sequences.

Item Type:Article
Subjects:Q Science > Q Science (General)
Divisions:Department of Bioinformatics
ID Code:1782
Deposited By: Prof. Matthias Bochtler
Deposited On:06 Dec 2019 09:00
Last Modified:06 Dec 2019 09:00

Repository Staff Only: item control page