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How plants pass down genetic memories

Photo of Arabidopsis thaliana plant
Arabidopsis thaliana is a plant species widely used to make fundamental biological discoveries. With the help of this versatile test subject, CSHL scientists have now dug up the secrets of a process that helps control inheritance.
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When organisms pass their genes on to future generations, they include more than the code spelled out in DNA. Some also pass along chemical markers that instruct cells how to use that code. The passage of these markers to future generations is known as epigenetic inheritance. It’s particularly common in plants. So, significant findings here may have implications for agriculture, food supplies, and the environment.

Image of DDM1 cell division
This video shows DDM1 (green) at work during cell division. As chromosomes are duplicated, DDM1 latches onto chromosomes to allow for vital chemical markers to be tacked on. Then, as the cell divides in two, DDM1 exits, and another protein, H3.3 (red), binds to chromosomes to prevent excess markers from being added.

Cold Spring Harbor Laboratory (CSHL) Professors and HHMI Investigators Rob Martienssen and Leemor Joshua-Tor have been researching how plants pass along the markers that keep transposons inactive. Transposons are also known as jumping genes. When switched on, they can move around and disrupt other genes. To silence them and protect the genome, cells add regulatory marks to specific DNA sites. This process is called methylation.

Martienssen and Joshua-Tor have now shown how protein DDM1 makes way for the enzyme that places these marks on new DNA strands. Plant cells need DDM1 because their DNA is tightly packaged. To keep their genomes compact and orderly, cells wrap their DNA around packing proteins called histones. “But that blocks access to the DNA for all sorts of important enzymes,” Martienssen explains. Before methylation can occur, “you have to remove or slide the histones out of the way.”

Martienssen and former CSHL colleague Eric Richards first discovered DDM1 30 years ago. Since then, researchers have learned it slides DNA along its packing proteins to expose sites needing methylation. Martienssen likens the movement to a yo-yo gliding along a string. The histones “can move up and down the DNA, exposing parts of the DNA at a time, but never falling off,” he explains.

Through genetic and biochemical experiments, Martienssen pinpointed the exact histones DDM1 displaces. Joshua-Tor used cryo-electron microscopy to capture detailed images of the enzyme interacting with DNA and associated packing proteins. They were able to see how DDM1 grabs onto particular histones to remodel packaged DNA. “An unexpected bond that ties DDM1 together turned out to correspond to the first mutation found all those years ago,” Joshua-Tor says.

Illustration of DDM1 protein gripping onto DNA
This cartoon model illustrates, for the first time, where and how the DDM1 protein (purple) grips onto DNA (beige) during cell division.

The experiments also revealed how DDM1’s affinity for certain histones preserves epigenetic controls across generations. The team showed that a histone found only in pollen is resistant to DDM1 and acts as a placeholder during cell division. “It remembers where the histone was during plant development and retains that memory into the next generation,” Martienssen says.

Plants may not be alone here. Humans also depend on DDM1-like proteins to maintain DNA methylation. The new discovery may help explain how those proteins keep our genomes functional and intact.

Written by: Jennifer Michalowski, Science Writer | publicaffairs@cshl.edu | 516-367-8455


Funding

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National Institutes of Health, National Science Foundation Plant Genome Research Program, Howard Hughes Medical Institute, Wellcome Trust, European Research Council, Horizon 2020.

Citation

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Lee, S.C., et al., “Chromatin remodeling of histone H3 variants underlies epigenetic inheritance of DNA methylation”, Cell, August 28, 2023. DOI: 10.1016/j.cell.2023.08.001

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Animal Tissue Imaging “The Animal Imaging Shared Resource provides researchers with both expertise and access to state-of-the-art, non-invasive preclinical imaging modalities. These include optical, ultrasound, CT, SPECT, and PET. These scanners collectively offer the researcher a high degree of experimental flexibility to non-invasively visualize and quantitate in vivo biology.” — Director Scott Lyons, Ph.D.

cryo EM “The Electron Cryomicroscopy (Cryo-EM) Facility offers researchers access to cutting-edge technology that has made it possible to visualize complex biological systems at near atomic resolution and detail, providing novel molecular insight into human biology and disease.” — Cryo-EM Facility Manager Dennis Thomas

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