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Posted: Nov 30, 2017
Scientists visualize structure of key DNA repair component with near-atomic resolution
(Nanowerk News) Cells continuously replicate to repair and replace damaged tissue, and each division requires a reprinting of the cell's genetic blueprints. As the DNA duplicates, errors inevitably occur, resulting in damage that, if left unrepaired, can lead to cellular death.
At the first hint of DNA damage, a protein known as an ATR kinase activates the cell's built-in repair system. Scientists have now imaged this protein at unprecedented resolution, and are beginning to understand its response to DNA damage.
Three-dimensional structure of the yeast Mec1-Ddc2 complex, a homolog of human ATR-ATRIP. The genomes of eukaryotic cells are under continuous assault by external and internal factors. All cells have elaborate mechanisms to maintain their genomes and the ATR kinase is a master regulator of genomic stability. The two Mec1-Ddc2 monomers directly contact head-to-head through the upper catalytic core, which can immediately culminate in full kinase activity upon DNA damage. (Image: Guoyan Wang and Yanbing Ma;structure based on the cryo-EM map of a yeast Mec1-Ddc2 complex)
"The ATR protein is the apical kinase to cope with the DNA damages and replication stress," said Gang Cai, a professor of life sciences at the University of Science & Technology of China in Hefei, China, and the lead author on the paper. "It has long been a central question to determine [the] activation mechanism of ATR kinase--how it responds to DNA damage and how it is activated."
Cai and his team used electron microscopy to image the Mec1-Ddc2 complex at 3.9 ångströms, which is about eight times the size of a single atom of helium. The complex is found in yeast and is the equivalent of the human ATR protein and its cell-signaling protein partner, ATRIP.
The ATR kinase is one of six proteins responsible for maintaining the health of the cell. When this family of proteins identify a problem, such as DNA damage, they instigate the downstream signals needed to repair the damage.
"Cryo-electron microscopy of the Mec1-Ddc2 with state-of-the-art instrumentation has resulted in an electron density map at near-atomic resolution," said Cai, noting that the improved map has confirmed and expanded upon previous findings.
ATR has long been a potential therapeutic target, according to Cai. The high-resolution structural information revealed regulatory sites of the ATR kinase, which are poised to activate at the first hint of DNA damage. Elucidating this mechanism could aid in the development of new therapeutics.
"The structure of [the] yeast member closely resembles those of the human counterpart," said Cai, drawing attention to the substantial similarity in the detailed architecture. "We believe the information acquired from the yeast Mec1-Ddc2 shed light on the architecture and mechanism of [the] human ATR-ATRIP complex."
Cai and his team are now imaging the yeast Mec1-Ddc2 and its human counterpart at different points of activation. They plan to develop more specific and efficient ATR inhibitors to explore the possibility of improving cancer treatments.
Source: University of Science and Technology of China