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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2020
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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. |
format | Online Article Text |
id | pubmed-7673738 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
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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