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Courtesy of Gerhard Schratt
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The paper:
G.M. Schratt et al., "A brain–specific microRNA regulates dendritic
spine development,"
Nature, 439:283–8, 2006. (Cited in 98 papers)
The finding:
In 2006, Michael Greenberg's group at Harvard Medical School and
Austrian colleagues hypothesized that microRNAs are involved in the
regulation of protein synthesis in neuronal dendrites. To test this, they
overexpressed a hippocampal microRNA, miR-134, and found that it reduced the
size of dendritic spines by inhibiting a protein kinase that induces spine
development.
The impact:
"Until that paper people thought of microRNAs as having more
constitutive roles," such as permanently repressing the translation of an
mRNA, says Kenneth Kosik at the University of California, Santa Barbara.
Instead, this study showed for the first time that microRNAs may also play a role
in synaptic plasticity and the modulation of translation.
The others:
In 2007 Kosik published evidence that nearly all microRNAs present in
the neuron's cell body are also present in the dendrite (
RNA, 13:1224–34, 2007). Kosik says miR-134 was present in a
concentration comparable to the other microRNAs.
The follow up:
First author Gerhard Schratt, now at the University of Heidelberg, is
interested in how those other microRNAs might be involved in synaptic
plasticity. His lab has found (but not yet published) another neuronal microRNA
that works opposite to miR-134 and promotes dendritic spine development.
Schratt supposes there is a network of microRNAs for fine-tuning the
synapse.
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Consequences of changing miR-134 expression: |
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Overexpression: 16.9% reduction in dendritic spine width |
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Inhibition: 7.6% increase in dendritic spine width |