黑料吃瓜资源

A new study in Nature by CSHL Professor Rob Martienssen and his group describes a new role for RNAi during chromosomal replication, one that allows the DNA replication process to progress smoothly without resulting in DNA damage.

Cold Spring Harbor, NY — At the same time that a cell鈥檚 DNA gets duplicated, a third of it gets super-compacted into repetitive clumps called heterochromatin. This dense packing serves to repress or 鈥渟ilence鈥� the DNA sequences within—which could wreck the genome if activated—as well as regulate the activity of nearby genes. When the cell divides, the daughter cells not only inherit a copy of the mother cell鈥檚 DNA, but also the exact pattern in which that DNA is clumped into heterochromatin.

This 鈥渆pigenetic鈥� mode of inheritance—information not transmitted through the DNA code itself but by the way in which it is packaged—has long been investigated by 黑料吃瓜资源 Professor and HHMI-GBMF Investigator Rob Martienssen. In a landmark study that was hailed as one of the in 2002, Martienssen and his colleagues showed that the inheritance of heterochromatin depends on a set of mechanisms broadly defined as RNA interference (RNAi).

In a new study that appeared online ahead of print in Nature on October 16, Martienssen鈥檚 team, including investigators from the Pasteur Institut in Paris and the University of Salamanca in Spain, describes a new role for RNAi, one that allows the DNA replication process itself to progress smoothly without resulting in DNA damage.

DNA is normally coiled around proteins called histones, which when chemically modified at specific locations, aggregate into dense arrays to form heterochromatin. Martienssen and others had previously found that RNAi guides this histone modification process, which occurs at the same time in the cell cycle when DNA is being duplicated.

In this RNAi-guided process, an enzyme called RNA polymerase II copies or 鈥渢ranscribes鈥� specific regions of DNA into RNA molecules, and somehow this modifies histones in those exact regions, thereby creating heterochromatin.

These heterochromatic regions, however, alternate with so-called 鈥渙rigins of replication鈥�—spots on the DNA where DNA-building proteins can bind, unzip the double-stranded DNA molecule to create a replication 鈥渇ork,鈥� and begin to build a new strand of it.

This alternate arrangement of regions to be transcribed for heterochromatin assembly and regions that serve as origins for DNA replication raised a new question: how do the transcription machinery and the replication machinery work in tandem without colliding with each other and as a result stall the replication fork and trigger DNA damage?

In a , Martienssen collaborated with scientists at the University of California at Berkeley and showed that the DNA-building proteins themselves could latch on to histone-modifying proteins and pull them along the replication fork.

鈥淭his finding raised the question of what role RNAi actually plays during the replication phase of the cell cycle,鈥� says Martienssen. 鈥淭he answers to both questions turned out to be very simple and elegant.鈥�

His group鈥檚 experiments in fission yeast, a simple model system used for studying heterochromatin, show that when the RNA polymerase II enzyme has transcribed a stretch of DNA into RNA, the RNAi mechanism causes the enzyme to release its hold on the DNA and fall away. This allows the replication fork to progress smoothly and the DNA strands to be copied by the replication machinery. The histone-modifying proteins, which follow right along, establish heterochromatin.

The scientists found that failure or absence of the RNAi mechanism stalls replication, which triggers a strong 鈥淒NA damage鈥� alert within the cell. That鈥檚 when a repair mechanism called homologous recombination kicks in and repairs the stalled fork, but the ability to modify histones is lost.

鈥淭hese experiments have revealed the real role of RNAi during the cell鈥檚 replication phase, which is to protect cells from this sort of replication-associated fork damage,鈥� according to Martienssen.

Written by: Hema Bashyam, Science Writer | [email protected] | 516-367-8455

Funding

This work was supported by grants from the Spanish Ministry of Science and the .

Citation

鈥淩NAi promotes heterochromatic silencing through replication-coupled release of RNA Pol II鈥� appears online in Nature on October 16. The full citation is: Mikel Zaratiegui, Stephane Castel1, Danielle V. Irvine, Anna Kloc, Jie Ren, Fei Li, Elisa de Castro, Laura Mar谋麓n, An-Yun Chang, Derek Goto, W. Zacheus Cande, Francisco Antequera, Benoit Arcangioli & Robert A. Martienssen. The paper can be downloaded at using the doi 10.1038/nature10501.