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Identification and characterization of an R-Smad homologue (Hco-DAF-8) from Haemonchus contortus
BACKGROUND: Smad proteins are essential cellular mediators within the transforming growth factor-β (TGF-β) superfamily. They directly transmit incoming signals from the cell surface receptors to the nucleus. In spite of their functional importance, almost nothing is known about Smad proteins in para...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7119156/ https://www.ncbi.nlm.nih.gov/pubmed/32245505 http://dx.doi.org/10.1186/s13071-020-04034-0 |
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author | Li, Fang-Fang Gasser, Robin B. Liu, Feng Shan, Jia-Nan Di, Wen-Da He, Li Zhou, Cai-Xian Wang, Chun-Qun Fang, Rui Hu, Min |
author_facet | Li, Fang-Fang Gasser, Robin B. Liu, Feng Shan, Jia-Nan Di, Wen-Da He, Li Zhou, Cai-Xian Wang, Chun-Qun Fang, Rui Hu, Min |
author_sort | Li, Fang-Fang |
collection | PubMed |
description | BACKGROUND: Smad proteins are essential cellular mediators within the transforming growth factor-β (TGF-β) superfamily. They directly transmit incoming signals from the cell surface receptors to the nucleus. In spite of their functional importance, almost nothing is known about Smad proteins in parasitic nematodes including Haemonchus contortus, an important blood-sucking nematode of small ruminants. METHODS: Based on genomic and transcriptome data for H. contortus and using bioinformatics methods, a Smad homologue (called Hco-daf-8) was inferred from H. contortus and the structural characteristics of this gene and its encoded protein Hco-DAF-8 established. Using real-time PCR and immunofluorescence assays, temporal transcriptional and spatial expression profiles of Hco-daf-8 were studied. Gene rescue in Caenorhabditis elegans was then applied to assess the function of Hco-daf-8 and a specific inhibitor of human Smad3 (called SIS3) was employed to evaluate the roles of Hco-DAF-8 in H. contortus development. RESULTS: The features of Hco-DAF-8 (502 amino acids), including conserved R-Smad domains and residues of the L3-loop that determine pathway specificity, are consistent with a TGF-β type I receptor-activated R-Smad. The Hco-daf-8 gene was transcribed in all developmental stages of H. contortus studied, with a higher level of transcription in the fourth-stage larval (L4) females and the highest level in adult males. Hco-DAF-8 was expressed in the platymyarian muscular cells, intestine and reproductive system of adult stages. Gene rescue experiments showed that Hco-daf-8 was able to partially rescue gene function in a daf-8 deficient mutant strain of C. elegans, leading to a resumption of normal development. In H. contortus, SIS3 was shown to affect H. contortus development from the exsheathed third-stage larvae (L3s) to L4s in vitro. CONCLUSIONS: These findings suggest that Hco-DAF-8, encoded by the gene Hco-daf-8, is an important cellular mediator of H. contortus development via the TGF-β signalling pathway. They provide a basis for future explorations of Hco-DAF-8 and associated pathways in H. contortus and other important parasitic nematodes. [Image: see text] |
format | Online Article Text |
id | pubmed-7119156 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-71191562020-04-07 Identification and characterization of an R-Smad homologue (Hco-DAF-8) from Haemonchus contortus Li, Fang-Fang Gasser, Robin B. Liu, Feng Shan, Jia-Nan Di, Wen-Da He, Li Zhou, Cai-Xian Wang, Chun-Qun Fang, Rui Hu, Min Parasit Vectors Research BACKGROUND: Smad proteins are essential cellular mediators within the transforming growth factor-β (TGF-β) superfamily. They directly transmit incoming signals from the cell surface receptors to the nucleus. In spite of their functional importance, almost nothing is known about Smad proteins in parasitic nematodes including Haemonchus contortus, an important blood-sucking nematode of small ruminants. METHODS: Based on genomic and transcriptome data for H. contortus and using bioinformatics methods, a Smad homologue (called Hco-daf-8) was inferred from H. contortus and the structural characteristics of this gene and its encoded protein Hco-DAF-8 established. Using real-time PCR and immunofluorescence assays, temporal transcriptional and spatial expression profiles of Hco-daf-8 were studied. Gene rescue in Caenorhabditis elegans was then applied to assess the function of Hco-daf-8 and a specific inhibitor of human Smad3 (called SIS3) was employed to evaluate the roles of Hco-DAF-8 in H. contortus development. RESULTS: The features of Hco-DAF-8 (502 amino acids), including conserved R-Smad domains and residues of the L3-loop that determine pathway specificity, are consistent with a TGF-β type I receptor-activated R-Smad. The Hco-daf-8 gene was transcribed in all developmental stages of H. contortus studied, with a higher level of transcription in the fourth-stage larval (L4) females and the highest level in adult males. Hco-DAF-8 was expressed in the platymyarian muscular cells, intestine and reproductive system of adult stages. Gene rescue experiments showed that Hco-daf-8 was able to partially rescue gene function in a daf-8 deficient mutant strain of C. elegans, leading to a resumption of normal development. In H. contortus, SIS3 was shown to affect H. contortus development from the exsheathed third-stage larvae (L3s) to L4s in vitro. CONCLUSIONS: These findings suggest that Hco-DAF-8, encoded by the gene Hco-daf-8, is an important cellular mediator of H. contortus development via the TGF-β signalling pathway. They provide a basis for future explorations of Hco-DAF-8 and associated pathways in H. contortus and other important parasitic nematodes. [Image: see text] BioMed Central 2020-04-03 /pmc/articles/PMC7119156/ /pubmed/32245505 http://dx.doi.org/10.1186/s13071-020-04034-0 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Li, Fang-Fang Gasser, Robin B. Liu, Feng Shan, Jia-Nan Di, Wen-Da He, Li Zhou, Cai-Xian Wang, Chun-Qun Fang, Rui Hu, Min Identification and characterization of an R-Smad homologue (Hco-DAF-8) from Haemonchus contortus |
title | Identification and characterization of an R-Smad homologue (Hco-DAF-8) from Haemonchus contortus |
title_full | Identification and characterization of an R-Smad homologue (Hco-DAF-8) from Haemonchus contortus |
title_fullStr | Identification and characterization of an R-Smad homologue (Hco-DAF-8) from Haemonchus contortus |
title_full_unstemmed | Identification and characterization of an R-Smad homologue (Hco-DAF-8) from Haemonchus contortus |
title_short | Identification and characterization of an R-Smad homologue (Hco-DAF-8) from Haemonchus contortus |
title_sort | identification and characterization of an r-smad homologue (hco-daf-8) from haemonchus contortus |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7119156/ https://www.ncbi.nlm.nih.gov/pubmed/32245505 http://dx.doi.org/10.1186/s13071-020-04034-0 |
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