Sarcomeric pattern formation by actin cluster coalescence.

Contractile function of striated muscle cells depends crucially on the almost crystalline order of actin and myosin filaments in myofibrils, but the physical mechanisms that lead to myofibril assembly remains ill-defined. Passive diffusive sorting of actin filaments into sarcomeric order is kinetica...

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Main Authors: Benjamin M Friedrich, Elisabeth Fischer-Friedrich, Nir S Gov, Samuel A Safran
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS Computational Biology
Online Access:http://europepmc.org/articles/PMC3369942?pdf=render
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spelling doaj-db37e5ab516146b98be0ffb91d68f0842020-11-25T02:31:46ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582012-01-0186e100254410.1371/journal.pcbi.1002544Sarcomeric pattern formation by actin cluster coalescence.Benjamin M FriedrichElisabeth Fischer-FriedrichNir S GovSamuel A SafranContractile function of striated muscle cells depends crucially on the almost crystalline order of actin and myosin filaments in myofibrils, but the physical mechanisms that lead to myofibril assembly remains ill-defined. Passive diffusive sorting of actin filaments into sarcomeric order is kinetically impossible, suggesting a pivotal role of active processes in sarcomeric pattern formation. Using a one-dimensional computational model of an initially unstriated actin bundle, we show that actin filament treadmilling in the presence of processive plus-end crosslinking provides a simple and robust mechanism for the polarity sorting of actin filaments as well as for the correct localization of myosin filaments. We propose that the coalescence of crosslinked actin clusters could be key for sarcomeric pattern formation. In our simulations, sarcomere spacing is set by filament length prompting tight length control already at early stages of pattern formation. The proposed mechanism could be generic and apply both to premyofibrils and nascent myofibrils in developing muscle cells as well as possibly to striated stress-fibers in non-muscle cells.http://europepmc.org/articles/PMC3369942?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Benjamin M Friedrich
Elisabeth Fischer-Friedrich
Nir S Gov
Samuel A Safran
spellingShingle Benjamin M Friedrich
Elisabeth Fischer-Friedrich
Nir S Gov
Samuel A Safran
Sarcomeric pattern formation by actin cluster coalescence.
PLoS Computational Biology
author_facet Benjamin M Friedrich
Elisabeth Fischer-Friedrich
Nir S Gov
Samuel A Safran
author_sort Benjamin M Friedrich
title Sarcomeric pattern formation by actin cluster coalescence.
title_short Sarcomeric pattern formation by actin cluster coalescence.
title_full Sarcomeric pattern formation by actin cluster coalescence.
title_fullStr Sarcomeric pattern formation by actin cluster coalescence.
title_full_unstemmed Sarcomeric pattern formation by actin cluster coalescence.
title_sort sarcomeric pattern formation by actin cluster coalescence.
publisher Public Library of Science (PLoS)
series PLoS Computational Biology
issn 1553-734X
1553-7358
publishDate 2012-01-01
description Contractile function of striated muscle cells depends crucially on the almost crystalline order of actin and myosin filaments in myofibrils, but the physical mechanisms that lead to myofibril assembly remains ill-defined. Passive diffusive sorting of actin filaments into sarcomeric order is kinetically impossible, suggesting a pivotal role of active processes in sarcomeric pattern formation. Using a one-dimensional computational model of an initially unstriated actin bundle, we show that actin filament treadmilling in the presence of processive plus-end crosslinking provides a simple and robust mechanism for the polarity sorting of actin filaments as well as for the correct localization of myosin filaments. We propose that the coalescence of crosslinked actin clusters could be key for sarcomeric pattern formation. In our simulations, sarcomere spacing is set by filament length prompting tight length control already at early stages of pattern formation. The proposed mechanism could be generic and apply both to premyofibrils and nascent myofibrils in developing muscle cells as well as possibly to striated stress-fibers in non-muscle cells.
url http://europepmc.org/articles/PMC3369942?pdf=render
work_keys_str_mv AT benjaminmfriedrich sarcomericpatternformationbyactinclustercoalescence
AT elisabethfischerfriedrich sarcomericpatternformationbyactinclustercoalescence
AT nirsgov sarcomericpatternformationbyactinclustercoalescence
AT samuelasafran sarcomericpatternformationbyactinclustercoalescence
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