Cargando…
Anchoring skeletal muscle development and disease: the role of ankyrin repeat domain containing proteins in muscle physiology
The ankyrin repeat is a protein module with high affinity for other ankyrin repeats based on strong Van der Waals forces. The resulting dimerization is unusually resistant to both mechanical forces and alkanization, making this module exceedingly useful for meeting the extraordinary demands of muscl...
Autores principales: | , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Informa Healthcare
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2942773/ https://www.ncbi.nlm.nih.gov/pubmed/20515317 http://dx.doi.org/10.3109/10409238.2010.488217 |
_version_ | 1782186958410219520 |
---|---|
author | Tee, Jin-Ming Peppelenbosch, Maikel P. |
author_facet | Tee, Jin-Ming Peppelenbosch, Maikel P. |
author_sort | Tee, Jin-Ming |
collection | PubMed |
description | The ankyrin repeat is a protein module with high affinity for other ankyrin repeats based on strong Van der Waals forces. The resulting dimerization is unusually resistant to both mechanical forces and alkanization, making this module exceedingly useful for meeting the extraordinary demands of muscle physiology. Many aspects of muscle function are controlled by the superfamily ankyrin repeat domain containing proteins, including structural fixation of the contractile apparatus to the muscle membrane by ankyrins, the archetypical member of the family. Additionally, other ankyrin repeat domain containing proteins critically control the various differentiation steps during muscle development, with Notch and developmental stage-specific expression of the members of the Ankyrin repeat and SOCS box (ASB) containing family of proteins controlling compartment size and guiding the various steps of muscle specification. Also, adaptive responses in fully formed muscle require ankyrin repeat containing proteins, with Myotrophin/V-1 ankyrin repeat containing proteins controlling the induction of hypertrophic responses following excessive mechanical load, and muscle ankyrin repeat proteins (MARPs) acting as protective mechanisms of last resort following extreme demands on muscle tissue. Knowledge on mechanisms governing the ordered expression of the various members of superfamily of ankyrin repeat domain containing proteins may prove exceedingly useful for developing novel rational therapy for cardiac disease and muscle dystrophies. |
format | Text |
id | pubmed-2942773 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Informa Healthcare |
record_format | MEDLINE/PubMed |
spelling | pubmed-29427732010-09-21 Anchoring skeletal muscle development and disease: the role of ankyrin repeat domain containing proteins in muscle physiology Tee, Jin-Ming Peppelenbosch, Maikel P. Crit Rev Biochem Mol Biol Review Article The ankyrin repeat is a protein module with high affinity for other ankyrin repeats based on strong Van der Waals forces. The resulting dimerization is unusually resistant to both mechanical forces and alkanization, making this module exceedingly useful for meeting the extraordinary demands of muscle physiology. Many aspects of muscle function are controlled by the superfamily ankyrin repeat domain containing proteins, including structural fixation of the contractile apparatus to the muscle membrane by ankyrins, the archetypical member of the family. Additionally, other ankyrin repeat domain containing proteins critically control the various differentiation steps during muscle development, with Notch and developmental stage-specific expression of the members of the Ankyrin repeat and SOCS box (ASB) containing family of proteins controlling compartment size and guiding the various steps of muscle specification. Also, adaptive responses in fully formed muscle require ankyrin repeat containing proteins, with Myotrophin/V-1 ankyrin repeat containing proteins controlling the induction of hypertrophic responses following excessive mechanical load, and muscle ankyrin repeat proteins (MARPs) acting as protective mechanisms of last resort following extreme demands on muscle tissue. Knowledge on mechanisms governing the ordered expression of the various members of superfamily of ankyrin repeat domain containing proteins may prove exceedingly useful for developing novel rational therapy for cardiac disease and muscle dystrophies. Informa Healthcare 2010-08 2010-06-01 /pmc/articles/PMC2942773/ /pubmed/20515317 http://dx.doi.org/10.3109/10409238.2010.488217 Text en © 2010 Informa UK Ltd http://creativecommons.org/licenses/by/2.0/ This is an open access article distributed under the Supplemental Terms and Conditions for iOpenAccess articles published in Informa Healthcare journals (http://www.informaworld.com/mpp/uploads/iopenaccess_tcs.pdf) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Tee, Jin-Ming Peppelenbosch, Maikel P. Anchoring skeletal muscle development and disease: the role of ankyrin repeat domain containing proteins in muscle physiology |
title | Anchoring skeletal muscle development and disease: the role of ankyrin repeat domain containing proteins in muscle physiology |
title_full | Anchoring skeletal muscle development and disease: the role of ankyrin repeat domain containing proteins in muscle physiology |
title_fullStr | Anchoring skeletal muscle development and disease: the role of ankyrin repeat domain containing proteins in muscle physiology |
title_full_unstemmed | Anchoring skeletal muscle development and disease: the role of ankyrin repeat domain containing proteins in muscle physiology |
title_short | Anchoring skeletal muscle development and disease: the role of ankyrin repeat domain containing proteins in muscle physiology |
title_sort | anchoring skeletal muscle development and disease: the role of ankyrin repeat domain containing proteins in muscle physiology |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2942773/ https://www.ncbi.nlm.nih.gov/pubmed/20515317 http://dx.doi.org/10.3109/10409238.2010.488217 |
work_keys_str_mv | AT teejinming anchoringskeletalmuscledevelopmentanddiseasetheroleofankyrinrepeatdomaincontainingproteinsinmusclephysiology AT peppelenboschmaikelp anchoringskeletalmuscledevelopmentanddiseasetheroleofankyrinrepeatdomaincontainingproteinsinmusclephysiology |