Knowing what to keep and what to trash: how an enzyme distinguishes cellular messages
Tuesday, 05 August 2014
Every once in a while, we are forced to sort that stack of papers on the kitchen counter. Interspersed between the expired coupons and dozens of takeout menus are important documents like your car insurance or electric bill. So it is not an option to simply drop it all in the trash at once – you need to read through the messages to be sure that you don’t lose vital information.
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Dis3l2 is protein that preserves the character
of
stem cells by degrading specific messages. But
how does the enzyme know which messages to
destroy? CSHL researchers obtained a molecular
photograph (imaged on the left) of the protein
in
complex with a “poly-U” chain (in orange) that
marks messages for degradation. The poly-U
chain is inserted into a funnel-like structure
deep
within Dis3l2 (see cartoon on the right, poly-U
chain again in orange). Inside the funnel,
there
are more than a dozen contacts that capture the
poly-U mark so that the entire message can be
destroyed. Credit: Leemor Joshua-Tor,
Cold
Spring Harbor Laboratory.
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Dis3l2 is a molecular machine that helps to preserve the character of stem cells. It serves as the executioner of an elegant pathway that prevents stem cells from changing into other cell types. The protein does this by acting like a garbage disposal for messages in the cell, cutting them up until they no longer encode useful information. But Dis3l2 is necessarily highly specific. While it must degrade messages that would alter the fate of the stem cell, discarding the wrong message could have devastating consequences.
Therefore, Dis3l2 only targets specific messages that have been marked with a molecular flag, known as a “poly-U” chain. The enzyme ignores the majority of messages in the cell – those that go on to encode proteins and other critical messages – whose ends are decorated with a different type of chain, called “poly-A” tail.
The CSHL scientists set out to understand how Dis3l2 is able to read and distinguish between these two chains. In work published today in Nature, they used a type of molecular photography, known as X-ray crystallography, to observe the structure of Dis3l2 while bound to a poly-U chain.
“We saw that the enzyme looks a lot like funnel, quite wide at the top and narrow at the base,” says Joshua-Tor.
“The poly-U chain inserts itself into the depths of this funnel while the rest of the bulky message can remain in the wide mouth at the top.”
But how does the enzyme “read” the poly-U chain? Christopher Faehnle, PhD and Jack Walleshauser, lead authors on the paper, found that the interior of the funnel contains more than a dozen contacts that interact specifically with the poly-U chain.
“Together, all of these points create a sticky web that holds the poly-U sequence deep within the enzyme,” says Faehnle.
“But other chains don’t interact – they can slide right out. It has helped us understand how an enzyme can differentiate between two sequences in the cell.”
More than that, the work provides insight into how a stem cell maintains its identity.
“Misregulation of any step in this pathway leads to developmental disorders and cancer,” says Joshua-Tor.
“We now have a much better appreciation of the terminal step, a critical point of control.”
Source: Cold Spring Harbor Laboratory
Contact: Jaclyn Jansen
Reference:
Mechanism of Dis3l2 substrate recognition in the Lin28–let-7 pathway
Christopher Faehnle, Jack Walleshauser and Leemor Joshua-Tor
Nature, August 3, 2014, doi. 10.1038/nature13553
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For more on stem cells and cloning, go to CellNEWS at
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