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Scientists crack structure of a novel enzyme linked to cell growth and cancer

Date:
November 6, 2019
Source:
University of California - Riverside
Summary:
A research team has discovered the structure of a novel RNA-modifying enzyme, ZCCHC4, and identified the mechanism that controls how this enzyme recognizes its substrate. ZCCHC4 influences cell proliferation and has been linked to cancers. The discovery has applications in structure-based drug design against cancers.
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FULL STORY

RNA, or ribonucleic acid, is present in the cells of all living beings and required to synthesize proteins. A research team at the University of California, Riverside, has discovered the structure of a novel RNA-modifying enzyme, ZCCHC4, and identified the mechanism that controls how this enzyme recognizes its substrate.

ZCCHC4 influences cell proliferation and has been linked to cancers. It uniquely introduces one kind of RNA modification, N6-methyladenosine (m6A), into ribosomes, which are cell organelles made up of RNA molecules and protein.

The study, published in Nature Communications, explains how protein machineries in cells are regulated to target RNA molecules for m6A modification.

Jikui Song, an associate professor of biochemistry at UC Riverside who led the study, explained ZCCHC4 controls protein synthesis and cell proliferation by introducing an m6A modification into ribosomes. ZCCHC4, he added, is overexpressed in tumors associated with hepatocellular carcinoma -- the most common type of primary liver cancer.

"This is the first time anyone has determined the crystal structure of ZCCHC4," Song said. "Our discovery can be used for structure-based drug design against cancers and lead to a better understanding of how m6A, a modification associated with numerous biological processes, is installed on ribosomal RNA."

The m6A modification has received enormous attention in recent years due to the important role it plays in RNA metabolism and biology. How this modification is dynamically programmed and distributed in cells, however, remains poorly understood.

"The structure of ZCCHC4 provides an understanding of how this enzyme is wired to specifically act on '28S ribosomal RNA,'" Song said, noting a ribosome is assembled with differently sized subunits. 28S ribosomal RNA refers to the RNA component in the 28S ribosomal subunit. "We now understand that this enzyme is controlled by an 'autoinhibitory' mechanism that has been observed in many other cellular processes."

To crack the structure of ZCCHC4, Song's team first produced an enzymatically active and structurally rigid ZCCHC4 fragment. The researchers then coaxed this protein to crystallize. Finally, they diffracted the crystals using X-rays and analyzed the data, which led to the eventual discovery of ZCCHC4's structure.

Last year, Song's lab solved the crystal structure for an enzyme that plays a key role in DNA methylation, the process by which methyl groups are added to the DNA molecule.

Next, the research team will continue to explore how various DNA and RNA modifications in cells are created, which has strong implications in health and diseases.

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Story Source:

Materials provided by University of California - Riverside. Original written by Iqbal Pittalwala. Note: Content may be edited for style and length.


Journal Reference:

  1. Wendan Ren, Jiuwei Lu, Mengjiang Huang, Linfeng Gao, Dongxu Li, Gang Greg Wang, Jikui Song. Structure and regulation of ZCCHC4 in m6A-methylation of 28S rRNA. Nature Communications, 2019; 10 (1) DOI: 10.1038/s41467-019-12923-x

Cite This Page:

University of California - Riverside. "Scientists crack structure of a novel enzyme linked to cell growth and cancer." ScienceDaily. ScienceDaily, 6 November 2019. <www.sciencedaily.com/releases/2019/11/191106085445.htm>.
University of California - Riverside. (2019, November 6). Scientists crack structure of a novel enzyme linked to cell growth and cancer. ScienceDaily. Retrieved September 25, 2023 from www.sciencedaily.com/releases/2019/11/191106085445.htm
University of California - Riverside. "Scientists crack structure of a novel enzyme linked to cell growth and cancer." ScienceDaily. www.sciencedaily.com/releases/2019/11/191106085445.htm (accessed September 25, 2023).

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