Messenger RNAs are regulated in far more ways than previously appreciated, study finds

Jun 25, 2010

One way of regulating protein levels in cells is to shorten the lifespan of messenger RNAs (mRNAs). These are intermediary molecules that are first copied from DNA in the cell's nucleus via a process called transcription and then transported into the cell's body to be translated into protein.

A team of molecular biologists from Cold Spring Harbor Laboratory (CSHL) has now discovered that mRNAs can be targeted for destruction by several modes and molecules, highlighting a previously unanticipated complexity in the control and regulation of the cell's genetic messages. Their findings are detailed in a paper that appears in Molecular Cell on June 25th.

"In addition to revealing the surprising diversity of post-transcriptional events that regulate mRNAs, our work also points to new roles for a family of proteins that mediate or RNAi," said CSHL Professor and HHMI Investigator Gregory Hannon, Ph.D., who led the team.

In RNAi, tiny bits of RNA that are about 21 "letters" or nucleotides long latch on to longer strands at regions where their nucleotide sequences are complementary. The tiny RNAs, called microRNAs, serve as guides to a family of proteins called Argonautes. The binding of the microRNA-Argonaute complex to its mRNA target triggers its destruction.

In mammals, this destruction has, until now, mostly been attributed to the activation of that destabilize the mRNA molecule, causing it to decay. By using a method that combines computational predictions with experimental testing, Hannon's group has now detected other modes of mRNA destruction that involve cleavage of mRNAs by various catalytic, or slicing, enzymes.

The team, which profiled the entire population of cleaved mRNAs found in mouse , has found multiple mRNAs that have undergone "endonucleolytic cleavage" - i.e. they have been sliced or cleaved (and hence destroyed) by the enzyme Ago2, one of the Argonautes. By sorting through cleaved mRNAs found in that lack Ago2 activity, the team has also found evidence that mRNAs also undergo cleavage by enzymes other than Ago2.

"One of these enzymes is another well known RNAi mediator called Drosha, which, like Ago2, also seems to be able to directly cleave its mRNA targets," explains Fedor Karginov, Ph.D., a postdoctoral researcher in Hannon's group. "But we're found many mRNA targets that aren't cleaved either by Ago2 or by Drosha, which suggests that there are other enzymes involved in regulating the life-spans of mRNAs."

"We've long wondered why Ago2's catalytic activity has been conserved in vertebrates - organisms in which microRNAs can for the most part operate without enzymatic help from Ago2," explains Hannon. "Our new findings of Ago2's direct involvement in mRNA regulation now help explain some of this evolutionary pressure to maintain a catalytically active Ago2 in mammals."

Explore further: Two-armed control of ATR, a master regulator of the DNA damage checkpoint

More information: "Diverse endonucleolytic cleavage sites in the mammalian transcriptome depend on microRNAs, Drosha, and additional nucleases," appears online in Molecular Cell on June 25th. The paper can be found at www.cell.com/molecular-cell/fu… 1097-2765(10)00416-8

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efrenjo
Jun 25, 2010
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nanotech_republika_pl
not rated yet Jun 26, 2010
The embeded page link to the paper is set incorrectly at the end of this article. The whole address should be copied and pasted.

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