DNA sequence variation in a population. A SNP is just a single nucleotide difference in the genome. The upper DNA molecule differs from the lower DNA molecule at a single base-pair location SNP model by David Eccles (gringer), CC BY 4.0 , via Wikimedia Commons
Medicine

Researchers Use AI to Decode Key DNA Sequence in Gene Activation

Machine learning unlocks identity of the ‘initiator’ and opens new predictions of DNA mutations that cause disease

Author : MBT Desk

Precise activation of tens of thousands of genes is critical for healthy development and growth. Specialized segments of our DNA are responsible for carefully orchestrating genetic sequences that result in the production of enzymes, hormones, proteins and other crucial components underlying cell structure and function. But if these genes are not correctly activated, cells can stop functioning or result in various disorders, including cancer.

To fully understand specific sequences within DNA that enable gene activation, researchers in University of California San Diego Professor James T. Kadonaga’s laboratory set out to decipher an important segment of DNA known as the “initiator.” This is the site at which the instructions coded in genes are first converted, or expressed, into functional products.

Ultimately, within the six billion bases of DNA in each of our cells, there is a gene expression code that specifies when, where and to what extent each of our genes should be turned on or off. If we had an AI model for the entire gene expression code, we would be able to predict the activity of each of the different variants of genes in different people. The new AI model for the initiator is a small but important part of this gene expression code, and I am optimistic that we will expand our AI models of the human gene expression code in the not-too-distant future.
James T. Kadonaga, Professor in the UC San Diego Department of Molecular Biology, School of Biological Sciences.

In the new study led by graduate student researcher Torrey Rhyne-Carrigg, scientists used high-throughput DNA sequencing technology to determine the gene expression activity of approximately 500,000 different versions of the initiator. With this information, they employed machine learning, a type of artificial intelligence, to create an AI model that then decoded the initiator’s signature DNA pattern. With the initiator’s DNA identity unmasked, the researchers could then search for its telltale sequence, finding that about 60% of human genes contain the initiator.

“These AI models were found to provide, for the first time, strong predictions of the presence or absence of the initiator in human genes, and were thus able to decode the DNA base sequence pattern of the initiator,” said Kadonaga, a professor in the UC San Diego Department of Molecular Biology, School of Biological Sciences.

Step 2 of DNA Replication: Creation of new strand with DNA polymerase

The newly uncovered information gives researchers the ability to predict the effects of DNA mutations that can lead to various disorders tied to the initiator. The data and models resulting from the new study could also be used to design synthetic promoters, sequences that turn genes on and off, with customized functions. More globally, this work is a step forward in the combined use of laboratory experiments and AI to decipher the information that is embedded in the sequence of the DNA bases in humans,” said Kadonaga.

( Newswise/MF)

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