Journal
DEVELOPMENTAL CELL
Volume 43, Issue 3, Pages 265-+Publisher
CELL PRESS
DOI: 10.1016/j.devcel.2017.10.003
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Funding
- HFSP long-term postdoctoral fellowship [LT000257/2009, LT000739/2012]
- Marie Curie International Outgoing Fellowship [FP7-PEOPLE-2011-IOF/301610]
- National Science Foundation [IBN-0615752, IOS-1355018]
- Alexander von Humboldt Professorship
- Direct For Biological Sciences
- Division Of Integrative Organismal Systems [1355018] Funding Source: National Science Foundation
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Small RNAs have emerged as a new class of mobile signals. Here, we investigate their mechanism of action and show that mobile small RNAs generate sharply defined domains of target gene expression through an intrinsic and direct threshold-based readout of their mobility gradients. This readout is highly sensitive to small RNA levels at the source, allowing plasticity in the positioning of a target gene expression boundary. Besides patterning their immediate targets, the readouts of opposing small RNA gradients enable specification of robust, uniformly positioned developmental boundaries. These patterning properties of small RNAs are reminiscent of those of animal morphogens. However, their mode of action and the intrinsic nature of their gradients distinguish mobile small RNAs from classical morphogens and present a unique direct mechanism through which to relay positional information. Mobile small RNAs and their targets thus emerge as highly portable, evolutionarily tractable regulatory modules through which to create pattern.
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