Summary information and primary citation
- PDB-id
-
8vdt;
DSSR-derived features in text and
JSON formats; DNAproDB
- Class
- ligase-DNA
- Method
- X-ray (2.78 Å)
- Summary
- DNA ligase 1 with nick DNA 3'ra:t
- Reference
-
Balu KE, Gulkis M, Almohdar D, Caglayan M (2024):
"Structures
of LIG1 provide a mechanistic basis for understanding a
lack of sugar discrimination against a ribonucleotide at
the 3'-end of nick DNA." J.Biol.Chem.,
300, 107216. doi: 10.1016/j.jbc.2024.107216.
- Abstract
- Human DNA ligase 1 (LIG1) is the main replicative
ligase that seals Okazaki fragments during nuclear
replication and finalizes DNA repair pathways by joining
DNA ends of the broken strand breaks in the three steps of
the ligation reaction. LIG1 can tolerate the RNA strand
upstream of the nick, yet an atomic insight into the sugar
discrimination mechanism by LIG1 against a ribonucleotide
at the 3'-terminus of nick DNA is unknown. Here, we
determined X-ray structures of LIG1/3'-RNA-DNA hybrids and
captured the ligase during pre- and post-step 3 the
ligation reaction. Furthermore, the overlays of 3'-rA:T and
3'-rG:C step 3 structures with step 2 structures of
canonical 3'-dA:T and 3'-dG:C uncover a network of LIG1/DNA
interactions through Asp570 and Arg871 side chains with
2'-OH of the ribose at nick showing a final phosphodiester
bond formation and the other ligase active site residues
surrounding the AMP site. Finally, we demonstrated that
LIG1 can ligate the nick DNA substrates with pre-inserted
3'-ribonucleotides as efficiently as Watson-Crick
base-paired ends in vitro. Together, our findings
uncover a novel atomic insight into a lack of sugar
discrimination by LIG1 and the impact of improper sugar on
the nick sealing of ribonucleotides at the last step of DNA
replication and repair.