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Expression of acyl-CoA-binding protein 5 from Rhodnius prolixus and its inhibition by RNA interference
The acyl-CoA-binding proteins (ACBP) act by regulating the availability of acyl-CoA in the cytoplasm and must have essential functions in lipid metabolism. The genome of the kissing-bug Rhodnius prolixus encodes five proteins of this family, but little is known about them. In this study we investiga...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6959561/ https://www.ncbi.nlm.nih.gov/pubmed/31935250 http://dx.doi.org/10.1371/journal.pone.0227685 |
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author | Almeida, Muriel G. M. D. Arêdes, Daniela S. Majerowicz, David Færgeman, Nils J. Knudsen, Jens Gondim, Katia C. |
author_facet | Almeida, Muriel G. M. D. Arêdes, Daniela S. Majerowicz, David Færgeman, Nils J. Knudsen, Jens Gondim, Katia C. |
author_sort | Almeida, Muriel G. M. D. |
collection | PubMed |
description | The acyl-CoA-binding proteins (ACBP) act by regulating the availability of acyl-CoA in the cytoplasm and must have essential functions in lipid metabolism. The genome of the kissing-bug Rhodnius prolixus encodes five proteins of this family, but little is known about them. In this study we investigated the expression and function of RpACBP-5. Feeding induced RpACBP-5 gene expression in the posterior midgut, and an increase of about four times was observed two days after the blood meal. However, the amount of protein, which was only detected in this organ, did not change during digestion. The RpACBP-5 gene was also highly expressed in pre-vitellogenic and vitellogenic oocytes. Recombinant RpACBP-5 was shown to bind to acyl-CoA of different lengths, and it exhibited nanomolar affinity to lauroyl-CoA in an isothermal titration assay, indicating that RpACBP-5 is a functional ACBP. RpACBP-5 knockdown by RNA interference did not affect digestion, egg laying and hatching, survival, or accumulation of triacylglycerol in the fat body and oocytes. Similarly, double knockdown of RpACBP-1 and RpACBP-5 did not alter egg laying and hatching, survival, accumulation of triacylglycerol in the fat body and oocytes, or the neutral lipid composition of the posterior midgut or hemolymph. These results show that RpACBP-5 is a functional ACBP but indicate that the lack of a detectable phenotype in the knockdown insects may be a consequence of functional overlap of the proteins of the ACBP family found in the insect. |
format | Online Article Text |
id | pubmed-6959561 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-69595612020-01-26 Expression of acyl-CoA-binding protein 5 from Rhodnius prolixus and its inhibition by RNA interference Almeida, Muriel G. M. D. Arêdes, Daniela S. Majerowicz, David Færgeman, Nils J. Knudsen, Jens Gondim, Katia C. PLoS One Research Article The acyl-CoA-binding proteins (ACBP) act by regulating the availability of acyl-CoA in the cytoplasm and must have essential functions in lipid metabolism. The genome of the kissing-bug Rhodnius prolixus encodes five proteins of this family, but little is known about them. In this study we investigated the expression and function of RpACBP-5. Feeding induced RpACBP-5 gene expression in the posterior midgut, and an increase of about four times was observed two days after the blood meal. However, the amount of protein, which was only detected in this organ, did not change during digestion. The RpACBP-5 gene was also highly expressed in pre-vitellogenic and vitellogenic oocytes. Recombinant RpACBP-5 was shown to bind to acyl-CoA of different lengths, and it exhibited nanomolar affinity to lauroyl-CoA in an isothermal titration assay, indicating that RpACBP-5 is a functional ACBP. RpACBP-5 knockdown by RNA interference did not affect digestion, egg laying and hatching, survival, or accumulation of triacylglycerol in the fat body and oocytes. Similarly, double knockdown of RpACBP-1 and RpACBP-5 did not alter egg laying and hatching, survival, accumulation of triacylglycerol in the fat body and oocytes, or the neutral lipid composition of the posterior midgut or hemolymph. These results show that RpACBP-5 is a functional ACBP but indicate that the lack of a detectable phenotype in the knockdown insects may be a consequence of functional overlap of the proteins of the ACBP family found in the insect. Public Library of Science 2020-01-14 /pmc/articles/PMC6959561/ /pubmed/31935250 http://dx.doi.org/10.1371/journal.pone.0227685 Text en © 2020 Almeida et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Almeida, Muriel G. M. D. Arêdes, Daniela S. Majerowicz, David Færgeman, Nils J. Knudsen, Jens Gondim, Katia C. Expression of acyl-CoA-binding protein 5 from Rhodnius prolixus and its inhibition by RNA interference |
title | Expression of acyl-CoA-binding protein 5 from Rhodnius prolixus and its inhibition by RNA interference |
title_full | Expression of acyl-CoA-binding protein 5 from Rhodnius prolixus and its inhibition by RNA interference |
title_fullStr | Expression of acyl-CoA-binding protein 5 from Rhodnius prolixus and its inhibition by RNA interference |
title_full_unstemmed | Expression of acyl-CoA-binding protein 5 from Rhodnius prolixus and its inhibition by RNA interference |
title_short | Expression of acyl-CoA-binding protein 5 from Rhodnius prolixus and its inhibition by RNA interference |
title_sort | expression of acyl-coa-binding protein 5 from rhodnius prolixus and its inhibition by rna interference |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6959561/ https://www.ncbi.nlm.nih.gov/pubmed/31935250 http://dx.doi.org/10.1371/journal.pone.0227685 |
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