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Evolution of insect proteomes: insights into synapse organization and synaptic vesicle life cycle

BACKGROUND: The molecular components in synapses that are essential to the life cycle of synaptic vesicles are well characterized. Nonetheless, many aspects of synaptic processes, in particular how they relate to complex behaviour, remain elusive. The genomes of flies, mosquitoes, the honeybee and t...

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Autores principales: Yanay, Chava, Morpurgo, Noa, Linial, Michal
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2374702/
https://www.ncbi.nlm.nih.gov/pubmed/18257909
http://dx.doi.org/10.1186/gb-2008-9-2-r27
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author Yanay, Chava
Morpurgo, Noa
Linial, Michal
author_facet Yanay, Chava
Morpurgo, Noa
Linial, Michal
author_sort Yanay, Chava
collection PubMed
description BACKGROUND: The molecular components in synapses that are essential to the life cycle of synaptic vesicles are well characterized. Nonetheless, many aspects of synaptic processes, in particular how they relate to complex behaviour, remain elusive. The genomes of flies, mosquitoes, the honeybee and the beetle are now fully sequenced and span an evolutionary breadth of about 350 million years; this provides a unique opportunity to conduct a comparative genomics study of the synapse. RESULTS: We compiled a list of 120 gene prototypes that comprise the core of presynaptic structures in insects. Insects lack several scaffolding proteins in the active zone, such as bassoon and piccollo, and the most abundant protein in the mammalian synaptic vesicle, namely synaptophysin. The pattern of evolution of synaptic protein complexes is analyzed. According to this analysis, the components of presynaptic complexes as well as proteins that take part in organelle biogenesis are tightly coordinated. Most synaptic proteins are involved in rich protein interaction networks. Overall, the number of interacting proteins and the degrees of sequence conservation between human and insects are closely correlated. Such a correlation holds for exocytotic but not for endocytotic proteins. CONCLUSION: This comparative study of human with insects sheds light on the composition and assembly of protein complexes in the synapse. Specifically, the nature of the protein interaction graphs differentiate exocytotic from endocytotic proteins and suggest unique evolutionary constraints for each set. General principles in the design of proteins of the presynaptic site can be inferred from a comparative study of human and insect genomes.
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spelling pubmed-23747022008-05-09 Evolution of insect proteomes: insights into synapse organization and synaptic vesicle life cycle Yanay, Chava Morpurgo, Noa Linial, Michal Genome Biol Research BACKGROUND: The molecular components in synapses that are essential to the life cycle of synaptic vesicles are well characterized. Nonetheless, many aspects of synaptic processes, in particular how they relate to complex behaviour, remain elusive. The genomes of flies, mosquitoes, the honeybee and the beetle are now fully sequenced and span an evolutionary breadth of about 350 million years; this provides a unique opportunity to conduct a comparative genomics study of the synapse. RESULTS: We compiled a list of 120 gene prototypes that comprise the core of presynaptic structures in insects. Insects lack several scaffolding proteins in the active zone, such as bassoon and piccollo, and the most abundant protein in the mammalian synaptic vesicle, namely synaptophysin. The pattern of evolution of synaptic protein complexes is analyzed. According to this analysis, the components of presynaptic complexes as well as proteins that take part in organelle biogenesis are tightly coordinated. Most synaptic proteins are involved in rich protein interaction networks. Overall, the number of interacting proteins and the degrees of sequence conservation between human and insects are closely correlated. Such a correlation holds for exocytotic but not for endocytotic proteins. CONCLUSION: This comparative study of human with insects sheds light on the composition and assembly of protein complexes in the synapse. Specifically, the nature of the protein interaction graphs differentiate exocytotic from endocytotic proteins and suggest unique evolutionary constraints for each set. General principles in the design of proteins of the presynaptic site can be inferred from a comparative study of human and insect genomes. BioMed Central 2008 2008-02-07 /pmc/articles/PMC2374702/ /pubmed/18257909 http://dx.doi.org/10.1186/gb-2008-9-2-r27 Text en Copyright © 2008 Yanay et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Yanay, Chava
Morpurgo, Noa
Linial, Michal
Evolution of insect proteomes: insights into synapse organization and synaptic vesicle life cycle
title Evolution of insect proteomes: insights into synapse organization and synaptic vesicle life cycle
title_full Evolution of insect proteomes: insights into synapse organization and synaptic vesicle life cycle
title_fullStr Evolution of insect proteomes: insights into synapse organization and synaptic vesicle life cycle
title_full_unstemmed Evolution of insect proteomes: insights into synapse organization and synaptic vesicle life cycle
title_short Evolution of insect proteomes: insights into synapse organization and synaptic vesicle life cycle
title_sort evolution of insect proteomes: insights into synapse organization and synaptic vesicle life cycle
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2374702/
https://www.ncbi.nlm.nih.gov/pubmed/18257909
http://dx.doi.org/10.1186/gb-2008-9-2-r27
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