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Molecular code cracked: Code determines recognition of RNA molecules

Date:
August 20, 2012
Source:
University of Western Australia
Summary:
Scientists have cracked a molecular code that may open the way to destroying or correcting defective gene products, such as those that cause genetic disorders in humans.
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A molecular model of a PPR protein recognizing a specific RNA molecule. The identity of specific amino acid residues in the protein (colored sticks) determines the sequence of the RNA molecule it can bind.
Credit: Image courtesy of University of Western Australia

Scientists have cracked a molecular code that may open the way to destroying or correcting defective gene products, such as those that cause genetic disorders in humans.

The code determines the recognition of RNA molecules by a super-family of RNA-binding proteins called pentatricopeptide repeat (PPR) proteins.

When a gene is switched on, it is copied into RNA. This RNA is then used to make proteins that are required by the organism for all of its vital functions. If a gene is defective, its RNA copy and the proteins made from this will also be defective. This forms the basis of many terrible genetic disorders in humans.

RNA-binding PPR proteins could revolutionize the way we treat disease. Their secret is their versatility -- they can find and bind a specific RNA molecule, and have the capacity to correct it if it is defective, or destroy it if it is detrimental. They can also help ramp up production of proteins required for growth and development.

The new paper in PLoS Genetics describes for the first time how PPR proteins recognize their RNA targets via an easy-to-understand code. This mechanism mimics the simplicity and predictability of the pairing between DNA strands described by Watson and Crick 60 years ago, but at a protein/RNA interface.

This exceptional breakthrough comes from an international, interdisciplinary research team including UWA researchers Professor Ian Small and Aaron Yap from the ARC Centre for Excellence in Plant Energy Biology and Professor Charlie Bond and Yee Seng Chong from UWA's School of Chemistry and Biochemistry, along with Professor Alice Barkan's team at the University of Oregon. This research was publicly funded by the ARC and the WA State Government in Australia and the NSF in the USA.

"Many PPR proteins are vitally important, but we don't know what they do. Now we've cracked the code, we can find out," said ARC Plant Energy Biology Director Ian Small.

"What's more, we can now design our own synthetic proteins to target any RNA sequence we choose -- this should allow us to control the expression of genes in new ways that just weren't available before. The potential is really exciting."

"This discovery was made in plants but is applicable across many species as PPR proteins are found in humans and animals too," says Professor Bond.


Story Source:

The above story is based on materials provided by University of Western Australia. Note: Materials may be edited for content and length.


Journal Reference:

  1. Alice Barkan, Margarita Rojas, Sota Fujii, Aaron Yap, Yee Seng Chong, Charles S. Bond, Ian Small. A Combinatorial Amino Acid Code for RNA Recognition by Pentatricopeptide Repeat Proteins. PLoS Genetics, 2012; 8 (8): e1002910 DOI: 10.1371/journal.pgen.1002910

Cite This Page:

University of Western Australia. "Molecular code cracked: Code determines recognition of RNA molecules." ScienceDaily. ScienceDaily, 20 August 2012. <www.sciencedaily.com/releases/2012/08/120820093759.htm>.
University of Western Australia. (2012, August 20). Molecular code cracked: Code determines recognition of RNA molecules. ScienceDaily. Retrieved May 24, 2015 from www.sciencedaily.com/releases/2012/08/120820093759.htm
University of Western Australia. "Molecular code cracked: Code determines recognition of RNA molecules." ScienceDaily. www.sciencedaily.com/releases/2012/08/120820093759.htm (accessed May 24, 2015).

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