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HKUST scientists make breakthrough with high-performance computing

Image Credits: HKUST, Press Release

According to a recent press release, scientists from the Hong Kong University of Science and Technology (HKUST) have recently uncovered the mechanisms of how RNA polymerase II performs intrinsic cleavage reaction to proofread RNA transcriptions, shedding light on how misregulation of accurate transcription can lead to diseases including cancer and Alzheimer’s disease.

The message of life is encoded in our genomic DNA through transcription of messenger RNAs and translation of proteins to perform cellular functions. To ensure accurate transcription – a process that transcribes genomic DNA into messenger RNA by adding nucleotides one by one like letters in the alphabet, an enzyme called RNA polymerase II would synthesize and proofread messenger RNA to remove any misincorporated nucleotides that do not match with the DNA template.

While RNA polymerase II was known to be critical in ensuring the accuracy of transcription, it had been a long-standing puzzle as to how this enzyme accomplishes this difficult task.

Scientists have always been intrigued to find out the underlying mechanisms, as that could offer insights on how errors could be made during this otherwise highly-accurate transcription process, which may lead to various human diseases.

A research team led by the Associate Professor of Science in the Department of Chemistry and Department of Chemical and Biological Engineering at HKUST recently discovered the mechanism for RNA polymerase II to correct errors in RNA synthesis.

When a nucleotide is added by mistake, RNA polymerase II can rewind by moving backwards (called backtracking) and cleave this misincorporated nucleotide. The research team found that while specific amino acid residues of RNA polymerase II are critical for backtracking, cleavage of the misincorporated nucleotide only requires the RNA itself (i.e. phosphate oxygen of misincorporated nucleotide).

It was noted that RNA polymerase II is like a molecular machine in the cell. Nature cleverly designs this machine to catalyze two distinct chemical reactions in a single active site without getting mixed-up. While normal RNA synthesis requires specific amino acid residues of RNA polymerase II, we found that the removal of the mismatched nucleotide does not rely on any amino acid residues.

This molecular machine seamlessly coordinates these two functions in one active site. The team’s discovery offers valuable insights into how transcription may go wrong in ageing and diseased cells, and to what extent transcriptional errors may lead to various human diseases.

The researchers’ work was only possible with the large-scale high-performance computing resources mostly provided by the Shaheen Supercomputer in collaboration with King Abdullah University of Science and Technology (KAUST).

The team’s quantum mechanics and molecular dynamics calculations consumed 20 million CPU core hours in total.

It was noted that the lead scientist’s research interest lies in understanding complex biological and chemical processes using computational approaches. The computational work was conducted by a long-time HKUST affiliate and alumnus of HKUST.

Other corresponding authors include HKUST’s Research Assistant from Department of Chemistry, a professor from New York University, and a professor from the University of California, San Diego whose research group performed experiments to validate the predicted mechanisms from calculations.

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