In a nutshell:

  • Mechanism identified for producing piRNAs that silence jumping genes in reproductive cells
  • piRNAs and PIWI proteins chop jumping gene RNA into pieces to make new piRNAs
  • piRNAs then transported to nucleus to silence jumping gene DNA

Heidelberg, 9 July 2015 – DNA within reproductive cells is protected through a clever system of find and destroy: new research published in Cell Reports today lifts the veil on how this is done.

A European team of scientists has discovered how the cells produce tiny pieces of RNA – called piRNA – that identify and silence ‘jumping genes’ or transposons: genes that are able to change their position within the genome and therefore alter or disrupt the genetic code.

Comprising just 30 letters of genetic code, piRNA are only found within cells in the reproductive organs of animals, where ensuring the stability and integrity of DNA is of particularly vital importance. They bond to proteins called PIWI and guide them to the messenger RNA produced by the jumping genes, which the PIWI protein then destroys. They are also able to guide PIWI proteins to the jumping gene in the nucleus, which the PIWI protein silences, preventing it from creating more jumping gene RNA. Although piRNAs have been known about for many years, scientists have until now had very little understanding of exactly how the piRNAs that guide PIWI proteins to jumping genes in the nucleus are produced.

New piRNAs bind to a nuclear PIWI protein to repress the expression of the jumping gene in the nucleus.

In germline cells PIWI proteins silence the RNA from jumping genes by cutting them in sequences of ~30 nucleotides that will become piRNAs. These new piRNAs bind to a nuclear PIWI protein to repress the expression of the jumping gene in the nucleus. IMAGE: Ramesh Pillai/EMBL

The research, which involved groups from EMBL Grenoble and CEA-Grenoble,  tracked the action of piRNA by inserting an artificial ‘jumping gene’ into a fruit fly germ cell. The scientists were able to see the piRNA bind to a jumping gene messenger RNA in the cell’s cytoplasm and to the PIWI protein, which then cut the first section from the jumping gene mRNA to silence it.

But destroying the jumping gene mRNA was only the start of the process, as the team discovered. The PIWI protein and piRNA then continued to work their way along the jumping gene – in a process dubbed ‘inchworming’ by the researchers –  cutting off 30 letters of code at a time and converting these into new piRNAs. The new piRNAs were then loaded onto a PIWI protein that was able to travel to the cell nucleus, where the piRNAs could recognise the jumping gene within the DNA, enabling the PIWI protein to silence it.

“We expected simply to see the jumping gene being silenced in the cytoplasm, so were really surprised to see it get converted into new piRNAs that were specifically loaded onto the PIWI protein that silences transposons in the nucleus,” explains Ramesh Pillai, from EMBL Grenoble. “Creating copies clearly increases the number of piRNAs that are able to recognise that particular jumping gene, as they retain the ‘memory’ of the original. This means that once the PIWI protein from the nucleus is loaded with the new piRNAs, it’s able to target the right gene in the DNA and silence it more efficiently.”

While jumping genes provide some benefits, uncontrolled changes in the DNA of reproductive cells can lead to sterility. The team, involving Radha Raman Pandey and David Homolka from the Pillai lab, is now investigating whether the piRNAs follow the same ‘inchworm’ process  within mammalian cells, to take them a step closer to understanding the process within humans.

Source article:

Homolka, Raman Pandey, Goriaux et al. Cell Reports, 9 July 2015. DOI:10.1016/j.celrep.2015.06.030

Article abstract

PIWI proteins and PIWI-interacting RNAs (piRNAs) mediate repression of transposons in the animal gonads. Primary processing converts long single-stranded RNAs into ~30 nucleotide (nt) piRNAs, but their entry into the biogenesis pathway is unknown. Here, we demonstrate that an RNA element at the 5′ end of a piRNA cluster ─which we termed piRNA trigger sequence (PTS)─ can induce primary processing of any downstream sequence.  We propose that such signals are triggers for the generation of the original pool of piRNAs. We also demonstrate that endonucleolytic cleavage of a transcript by a cytosolic PIWI results in its entry into primary processing which triggers the generation of non-overlapping, contiguous primary piRNAs in the 3′ direction from the target transcript. These piRNAs are loaded into a nuclear PIWI thereby linking cytoplasmic post-transcriptional silencing to nuclear transcriptional repression.

This post was originally published on EMBL News.

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