The shrimp mitochondrial FoF1-ATPase inhibitory factor 1 (IF1)

The whiteleg shrimp species Litopenaeus vannamei is exposed to cyclic changes of the dissolved oxygen concentration of seawater and must neutralize the adverse effects of hypoxia by using ATP as energy source. In crustaceans, the mitochondrial FOF1-ATP synthase is pivotal to the homeostasis of ATP a...

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Autor principal: Chimeo, C.
Otros Autores: Fernandez-Gimenez, A.V, Campanella, M., Mendez-Romero, O., Muhlia-Almazan, A.
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: Springer New York LLC 2015
Acceso en línea:Registro en Scopus
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040 |a Scopus  |b spa  |c AR-BaUEN  |d AR-BaUEN 
030 |a JBBID 
100 1 |a Chimeo, C. 
245 1 4 |a The shrimp mitochondrial FoF1-ATPase inhibitory factor 1 (IF1) 
260 |b Springer New York LLC  |c 2015 
270 1 0 |m Muhlia-Almazan, A.; Bioenergetics and Molecular Genetics Lab, Centro de Investigacion en Alimentacion y Desarrollo (CIAD) A. C, Carretera a Ejido La Victoria Km 0.6, PO Box 1735, Mexico; email: amuhlia@ciad.mx 
506 |2 openaire  |e Política editorial 
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520 3 |a The whiteleg shrimp species Litopenaeus vannamei is exposed to cyclic changes of the dissolved oxygen concentration of seawater and must neutralize the adverse effects of hypoxia by using ATP as energy source. In crustaceans, the mitochondrial FOF1-ATP synthase is pivotal to the homeostasis of ATP and function prevalently as a FOF1-ATPase. Hitherto, it is unknown whether these marine invertebrates are equipped with molecules able to control the FOF1-ATPase inhibiting the ATP consumption. In this study, we report two variants of the mitochondrial FOF1-ATPase Inhibitory Factor 1 (IF1) ubiquitously expressed across tissues of the Litopenaeus vannamei transcriptome: the IF1_Lv1 and the IF1_Lv2. The IF1_Lv1, with a full-length sequence of 550 bp, encodes a 104 aa long protein and its mRNA amounts are significantly affected by hypoxia and re-oxygenation. The IF1_Lv2, with a sequence of 654 bp, encodes instead for a protein of 85 aa. Both proteins share a 69 % homology and contain a conserved minimal inhibitory sequence (IATP domain) along with a G-rich region on their N-terminus typical of the invertebrate. In light of this characterization IF1 is here discussed as an adaptive mechanism evolved by this marine species to inhibit the FOF1-ATPase activity and avoid ATP dissipation to thrive in spite of the changes in oxygen tension. © 2015, Springer Science+Business Media New York.  |l eng 
536 |a Detalles de la financiación: 241670, CONACYT, Consejo Nacional de Ciencia y Tecnología 
593 |a Bioenergetics and Molecular Genetics Lab, Centro de Investigacion en Alimentacion y Desarrollo (CIAD) A. C, Carretera a Ejido La Victoria Km 0.6, PO Box 1735, Hermosillo, Sonora, Mexico 
593 |a Laboratorio Fisiologia de Organismos Acuaticos. Instituto de Investigaciones Marinas y Costeras, Facultad de Ciencias Exactas y Naturales, Universidad Nacional de Mar del Plata, Buenos Aires, Argentina 
593 |a Department of Comparative Biomedical Sciences, The Royal Veterinary College, University of London, London, United Kingdom 
593 |a University College London Consortium for Mitochondrial Research, Royal College Street NW1 0TU, London, United Kingdom 
690 1 0 |a HYPOXIA 
690 1 0 |a IF1, FOF1-ATPASE 
690 1 0 |a INHIBITOR 
690 1 0 |a SHRIMP 
690 1 0 |a TRANSCRIPTIONAL REGULATION 
690 1 0 |a ADENOSINE TRIPHOSPHATASE 
690 1 0 |a COMPLEMENTARY DNA 
690 1 0 |a FIBRINOGEN 
690 1 0 |a INHIBITORY FACTOR 1 
690 1 0 |a MESSENGER RNA 
690 1 0 |a TRANSCRIPTOME 
690 1 0 |a UNCLASSIFIED DRUG 
690 1 0 |a ARTHROPOD PROTEIN 
690 1 0 |a ATPASE INHIBITORY PROTEIN 
690 1 0 |a PROTEIN 
690 1 0 |a PROTON TRANSPORTING ADENOSINE TRIPHOSPHATASE 
690 1 0 |a ADULT 
690 1 0 |a AMINO ACID SEQUENCE 
690 1 0 |a ANIMAL TISSUE 
690 1 0 |a ARTICLE 
690 1 0 |a CONTROLLED STUDY 
690 1 0 |a DNA SEQUENCE 
690 1 0 |a ENZYME ACTIVITY 
690 1 0 |a GENE EXPRESSION 
690 1 0 |a GENE SEQUENCE 
690 1 0 |a GENETIC VARIABILITY 
690 1 0 |a LITOPENAEUS VANNAMEI 
690 1 0 |a MARINE SPECIES 
690 1 0 |a MITOCHONDRION 
690 1 0 |a NONHUMAN 
690 1 0 |a NUCLEOTIDE SEQUENCE 
690 1 0 |a OXYGEN TENSION 
690 1 0 |a PHYLOGENY 
690 1 0 |a REOXYGENATION 
690 1 0 |a RNA SEQUENCE 
690 1 0 |a SEQUENCE HOMOLOGY 
690 1 0 |a ANIMAL 
690 1 0 |a GENETICS 
690 1 0 |a METABOLISM 
690 1 0 |a MOLECULAR GENETICS 
690 1 0 |a PENAEIDAE 
690 1 0 |a ANIMALS 
690 1 0 |a ARTHROPOD PROTEINS 
690 1 0 |a BASE SEQUENCE 
690 1 0 |a MOLECULAR SEQUENCE DATA 
690 1 0 |a PENAEIDAE 
690 1 0 |a PROTEINS 
690 1 0 |a PROTON-TRANSLOCATING ATPASES 
700 1 |a Fernandez-Gimenez, A.V. 
700 1 |a Campanella, M. 
700 1 |a Mendez-Romero, O. 
700 1 |a Muhlia-Almazan, A. 
773 0 |d Springer New York LLC, 2015  |g v. 47  |h pp. 383-393  |k n. 5  |x 0145479X  |t J. Bioenerg. Biomembr. 
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856 4 0 |u https://doi.org/10.1007/s10863-015-9621-0  |y DOI 
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