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Nebulin and Lmod2 are critical for specifying thin-filament length in skeletal muscle

Regulating the thin-filament length in muscle is crucial for controlling the number of myosin motors that generate power. The giant protein nebulin forms a long slender filament that associates along the length of the thin filament in skeletal muscle with functions that remain largely obscure. Here...

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Autores principales: Kiss, Balázs, Gohlke, Jochen, Tonino, Paola, Hourani, Zaynab, Kolb, Justin, Strom, Joshua, Alekhina, Olga, Smith, John E., Ottenheijm, Coen, Gregorio, Carol, Granzier, Henk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7673738/
https://www.ncbi.nlm.nih.gov/pubmed/33177085
http://dx.doi.org/10.1126/sciadv.abc1992
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author Kiss, Balázs
Gohlke, Jochen
Tonino, Paola
Hourani, Zaynab
Kolb, Justin
Strom, Joshua
Alekhina, Olga
Smith, John E.
Ottenheijm, Coen
Gregorio, Carol
Granzier, Henk
author_facet Kiss, Balázs
Gohlke, Jochen
Tonino, Paola
Hourani, Zaynab
Kolb, Justin
Strom, Joshua
Alekhina, Olga
Smith, John E.
Ottenheijm, Coen
Gregorio, Carol
Granzier, Henk
author_sort Kiss, Balázs
collection PubMed
description Regulating the thin-filament length in muscle is crucial for controlling the number of myosin motors that generate power. The giant protein nebulin forms a long slender filament that associates along the length of the thin filament in skeletal muscle with functions that remain largely obscure. Here nebulin’s role in thin-filament length regulation was investigated by targeting entire super-repeats in the Neb gene; nebulin was either shortened or lengthened by 115 nm. Its effect on thin-filament length was studied using high-resolution structural and functional techniques. Results revealed that thin-filament length is strictly regulated by the length of nebulin in fast muscles. Nebulin’s control is less tight in slow muscle types where a distal nebulin-free thin-filament segment exists, the length of which was found to be regulated by leiomodin-2 (Lmod2). We propose that strict length control by nebulin promotes high-speed shortening and that dual-regulation by nebulin/Lmod2 enhances contraction efficiency.
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spelling pubmed-76737382020-11-24 Nebulin and Lmod2 are critical for specifying thin-filament length in skeletal muscle Kiss, Balázs Gohlke, Jochen Tonino, Paola Hourani, Zaynab Kolb, Justin Strom, Joshua Alekhina, Olga Smith, John E. Ottenheijm, Coen Gregorio, Carol Granzier, Henk Sci Adv Research Articles Regulating the thin-filament length in muscle is crucial for controlling the number of myosin motors that generate power. The giant protein nebulin forms a long slender filament that associates along the length of the thin filament in skeletal muscle with functions that remain largely obscure. Here nebulin’s role in thin-filament length regulation was investigated by targeting entire super-repeats in the Neb gene; nebulin was either shortened or lengthened by 115 nm. Its effect on thin-filament length was studied using high-resolution structural and functional techniques. Results revealed that thin-filament length is strictly regulated by the length of nebulin in fast muscles. Nebulin’s control is less tight in slow muscle types where a distal nebulin-free thin-filament segment exists, the length of which was found to be regulated by leiomodin-2 (Lmod2). We propose that strict length control by nebulin promotes high-speed shortening and that dual-regulation by nebulin/Lmod2 enhances contraction efficiency. American Association for the Advancement of Science 2020-11-11 /pmc/articles/PMC7673738/ /pubmed/33177085 http://dx.doi.org/10.1126/sciadv.abc1992 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/ https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Kiss, Balázs
Gohlke, Jochen
Tonino, Paola
Hourani, Zaynab
Kolb, Justin
Strom, Joshua
Alekhina, Olga
Smith, John E.
Ottenheijm, Coen
Gregorio, Carol
Granzier, Henk
Nebulin and Lmod2 are critical for specifying thin-filament length in skeletal muscle
title Nebulin and Lmod2 are critical for specifying thin-filament length in skeletal muscle
title_full Nebulin and Lmod2 are critical for specifying thin-filament length in skeletal muscle
title_fullStr Nebulin and Lmod2 are critical for specifying thin-filament length in skeletal muscle
title_full_unstemmed Nebulin and Lmod2 are critical for specifying thin-filament length in skeletal muscle
title_short Nebulin and Lmod2 are critical for specifying thin-filament length in skeletal muscle
title_sort nebulin and lmod2 are critical for specifying thin-filament length in skeletal muscle
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7673738/
https://www.ncbi.nlm.nih.gov/pubmed/33177085
http://dx.doi.org/10.1126/sciadv.abc1992
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