Sensing and responding to hypoxia via HIF in model invertebrates

This past decade has brought considerable progress towards elucidating the molecular mechanisms of oxygen sensing pathways by which mammalian cells are able to detect and adjust, or succumb, to hypoxia. In contrast, far less is known about the protein and DNA constituents that endow many invertebrat...

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Autores principales: Gorr, T.A., Gassmann, M., Wappner, P.
Formato: JOUR
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fly
Acceso en línea:http://hdl.handle.net/20.500.12110/paper_00221910_v52_n4_p349_Gorr
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spelling todo:paper_00221910_v52_n4_p349_Gorr2023-10-03T14:28:15Z Sensing and responding to hypoxia via HIF in model invertebrates Gorr, T.A. Gassmann, M. Wappner, P. Daphnia Drosophila Hypometabolism Hypoxia-inducible factor Tracheogenesis basic helix loop helix transcription factor oxygen procollagen proline 2 oxoglutarate 4 dioxygenase fly hypoxia invertebrate mammal oxygen protein animal Caenorhabditis elegans Daphnia Drosophila melanogaster genetics growth, development and aging invertebrate mammal physiology review signal transduction Animals Basic Helix-Loop-Helix Transcription Factors Caenorhabditis elegans Daphnia Drosophila melanogaster Invertebrates Mammals Oxygen Procollagen-Proline Dioxygenase Signal Transduction Animalia Arthropoda Caenorhabditis elegans Crustacea Daphnia Daphnia magna Drosophila melanogaster Hexapoda Insecta Invertebrata Mammalia Nematoda This past decade has brought considerable progress towards elucidating the molecular mechanisms of oxygen sensing pathways by which mammalian cells are able to detect and adjust, or succumb, to hypoxia. In contrast, far less is known about the protein and DNA constituents that endow many invertebrate species to withstand and recover from even more severe and prolonged O2 limitations. In spite of these differences in hypoxia tolerance, inadequacy in oxygen supply is, from mammals to insects to nematodes, signaled onto the DNA level predominantly by hypoxia-inducible factors (HIFs). Across the animal kingdom, HIF accumulates in hypoxic, but not normoxic, cells and functions in a remarkably conserved pathway. Using crustacean (Daphnia magna) and insect (Drosophila melanogaster) models, work by us and others has implicated HIF in restoring O2 delivery via stimulated hemoglobin synthesis (Daphnia) or tracheal remodeling (Drosophila). HIF is essential for these arthropods to adapt and survive during moderate O2 limitations. A similar life-preserving role for HIF-signaling in hypoxic, but not anoxic, environments had previously been established for another stress-tolerant invertebrate model, the nematode Caenorhabditis elegans. Exploring regulations of oxygen-dependent Daphnia and Drosophila genes in cell culture and in vivo have furthermore aided in uncovering novel HIF-targeting mechanisms that might operate to fine-tune the activity of this transcription factor under steadily hypoxic, rather than changing, oxygen tensions. We conclude our review with yet another addition to the growing list of HIF's many functions: the control of cellular growth during fly development. © 2006 Elsevier Ltd. All rights reserved. Fil:Wappner, P. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_00221910_v52_n4_p349_Gorr
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Daphnia
Drosophila
Hypometabolism
Hypoxia-inducible factor
Tracheogenesis
basic helix loop helix transcription factor
oxygen
procollagen proline 2 oxoglutarate 4 dioxygenase
fly
hypoxia
invertebrate
mammal
oxygen
protein
animal
Caenorhabditis elegans
Daphnia
Drosophila melanogaster
genetics
growth, development and aging
invertebrate
mammal
physiology
review
signal transduction
Animals
Basic Helix-Loop-Helix Transcription Factors
Caenorhabditis elegans
Daphnia
Drosophila melanogaster
Invertebrates
Mammals
Oxygen
Procollagen-Proline Dioxygenase
Signal Transduction
Animalia
Arthropoda
Caenorhabditis elegans
Crustacea
Daphnia
Daphnia magna
Drosophila melanogaster
Hexapoda
Insecta
Invertebrata
Mammalia
Nematoda
spellingShingle Daphnia
Drosophila
Hypometabolism
Hypoxia-inducible factor
Tracheogenesis
basic helix loop helix transcription factor
oxygen
procollagen proline 2 oxoglutarate 4 dioxygenase
fly
hypoxia
invertebrate
mammal
oxygen
protein
animal
Caenorhabditis elegans
Daphnia
Drosophila melanogaster
genetics
growth, development and aging
invertebrate
mammal
physiology
review
signal transduction
Animals
Basic Helix-Loop-Helix Transcription Factors
Caenorhabditis elegans
Daphnia
Drosophila melanogaster
Invertebrates
Mammals
Oxygen
Procollagen-Proline Dioxygenase
Signal Transduction
Animalia
Arthropoda
Caenorhabditis elegans
Crustacea
Daphnia
Daphnia magna
Drosophila melanogaster
Hexapoda
Insecta
Invertebrata
Mammalia
Nematoda
Gorr, T.A.
Gassmann, M.
Wappner, P.
Sensing and responding to hypoxia via HIF in model invertebrates
topic_facet Daphnia
Drosophila
Hypometabolism
Hypoxia-inducible factor
Tracheogenesis
basic helix loop helix transcription factor
oxygen
procollagen proline 2 oxoglutarate 4 dioxygenase
fly
hypoxia
invertebrate
mammal
oxygen
protein
animal
Caenorhabditis elegans
Daphnia
Drosophila melanogaster
genetics
growth, development and aging
invertebrate
mammal
physiology
review
signal transduction
Animals
Basic Helix-Loop-Helix Transcription Factors
Caenorhabditis elegans
Daphnia
Drosophila melanogaster
Invertebrates
Mammals
Oxygen
Procollagen-Proline Dioxygenase
Signal Transduction
Animalia
Arthropoda
Caenorhabditis elegans
Crustacea
Daphnia
Daphnia magna
Drosophila melanogaster
Hexapoda
Insecta
Invertebrata
Mammalia
Nematoda
description This past decade has brought considerable progress towards elucidating the molecular mechanisms of oxygen sensing pathways by which mammalian cells are able to detect and adjust, or succumb, to hypoxia. In contrast, far less is known about the protein and DNA constituents that endow many invertebrate species to withstand and recover from even more severe and prolonged O2 limitations. In spite of these differences in hypoxia tolerance, inadequacy in oxygen supply is, from mammals to insects to nematodes, signaled onto the DNA level predominantly by hypoxia-inducible factors (HIFs). Across the animal kingdom, HIF accumulates in hypoxic, but not normoxic, cells and functions in a remarkably conserved pathway. Using crustacean (Daphnia magna) and insect (Drosophila melanogaster) models, work by us and others has implicated HIF in restoring O2 delivery via stimulated hemoglobin synthesis (Daphnia) or tracheal remodeling (Drosophila). HIF is essential for these arthropods to adapt and survive during moderate O2 limitations. A similar life-preserving role for HIF-signaling in hypoxic, but not anoxic, environments had previously been established for another stress-tolerant invertebrate model, the nematode Caenorhabditis elegans. Exploring regulations of oxygen-dependent Daphnia and Drosophila genes in cell culture and in vivo have furthermore aided in uncovering novel HIF-targeting mechanisms that might operate to fine-tune the activity of this transcription factor under steadily hypoxic, rather than changing, oxygen tensions. We conclude our review with yet another addition to the growing list of HIF's many functions: the control of cellular growth during fly development. © 2006 Elsevier Ltd. All rights reserved.
format JOUR
author Gorr, T.A.
Gassmann, M.
Wappner, P.
author_facet Gorr, T.A.
Gassmann, M.
Wappner, P.
author_sort Gorr, T.A.
title Sensing and responding to hypoxia via HIF in model invertebrates
title_short Sensing and responding to hypoxia via HIF in model invertebrates
title_full Sensing and responding to hypoxia via HIF in model invertebrates
title_fullStr Sensing and responding to hypoxia via HIF in model invertebrates
title_full_unstemmed Sensing and responding to hypoxia via HIF in model invertebrates
title_sort sensing and responding to hypoxia via hif in model invertebrates
url http://hdl.handle.net/20.500.12110/paper_00221910_v52_n4_p349_Gorr
work_keys_str_mv AT gorrta sensingandrespondingtohypoxiaviahifinmodelinvertebrates
AT gassmannm sensingandrespondingtohypoxiaviahifinmodelinvertebrates
AT wappnerp sensingandrespondingtohypoxiaviahifinmodelinvertebrates
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