Deep inside our cells鈥攅ach one complete with an identical set of genes鈥攁 molecular machine known as PRC2 plays a critical role in determining which cells become heart cells, versus brain or muscle or skin cells.
When the machine is missing or broken, normal fetal development can鈥檛 occur. If it鈥檚 mutated, cells can grow uncontrollably, and cancer can arise鈥攁 fact that has made PRC2 a source of keen interest for drug developers.
New research by scientists at 彩民宝典 and Harvard Medical School offers an unprecedented look at how PRC2, or polycomb repressive complex 2, does its job and, specifically, how ribonucleic acid (RNA) helps it switch genes on and off.
The findings, , shed new light on how development occurs and could pave the way for novel therapeutics for hard-to-treat cancers, including blood, pancreatic and colon cancer, leukemia and pediatric tumors.
鈥淲e know PRC2 is extremely important for development and for maintaining the identity of cells, and we know that RNA regulates it. But mechanistically, we didn鈥檛 know how,鈥� said co-senior author Vignesh Kasinath, assistant professor of biochemistry at 彩民宝典.
For the study, Kasinath鈥檚 lab collaborated with Nobel Laureate Thomas Cech and colleagues at the BioFrontiers Institute to photograph PRC2 in action, using state-of-the-art 鈥渃ryo-electron microscopy.鈥� The technique involves freezing samples to extremely cold temperatures to preserve their native structure and then hitting them with an electron beam at speeds nearly the speed of light to create ultra-high-resolution 3D images.
Previous research has shown that this enzyme complex, made of multiple proteins, is a potent gene-silencer, effectively shutting off access to specific regions of the genome so a stem cell can differentiate into a particular cell type. In a budding heart cell, for instance, it plays a role in silencing genes that might guide it to become a kidney or liver cell.
How that happens remained a mystery.
鈥淚f you think of PRC2 as a car, we know a lot about what happens when it gets to its destination, but we don鈥檛 know how to drive it there,鈥� said first author Jiarui Song, a Jane Coffin Childs postdoctoral fellow in the Cech Lab.
Catching development in a freezeframe听
To find out, the team synthesized PRC2 and RNA in the lab and used CU鈥檚 cutting-edge Titan Krios Electron Microscopy Facility, which enables researchers to image molecules at the atomic level, to take the first-ever picture of PRC2 and RNA bound together.
They discovered that when one RNA molecule grabs on to two PRC2 proteins it clamps them down like a clamshell with RNA as the hinge, essentially gluing together their surfaces so they can鈥檛 interact with DNA. In doing so, RNA effectively silences the silencer, enabling genes in certain regions of the genome to keep firing while others remain 鈥渙ff.鈥�
鈥淩NA essentially acts as a checkpoint, making sure PRC2 only acts on certain regions of the genome,鈥� said Kasinath.
Using biochemistry and additional experiments in zebrafish, the research team was able to confirm what they saw under the microscope in living cells.
The study is the first to define, at the molecular level, how RNA regulates PRC2 activity and could pave the way for more effective, targeted treatments for diseases where PRC2 regulation is defective.
鈥淯nderstanding this mechanism could enable the development of a new generation of RNA-based therapeutics. This work lays that foundation,鈥� said Kasinath.
Other co-authors include Anne Gooding, Wayne Hemphill and Liqi Yao of 彩民宝典 and Brittney Love, Anne Robertson, Leonard Zon and Trista North of Harvard Medical School.
