Cargando…

Gender-Associated Genes in Filarial Nematodes Are Important for Reproduction and Potential Intervention Targets

BACKGROUND: A better understanding of reproductive processes in parasitic nematodes may lead to development of new anthelmintics and control strategies for combating disabling and disfiguring neglected tropical diseases such as lymphatic filariasis and onchocerciasis. Transcriptomatic analysis has p...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Ben-Wen, Rush, Amy C., Jiang, Dao-Jun, Mitreva, Makedonka, Abubucker, Sahar, Weil, Gary J.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3026763/
https://www.ncbi.nlm.nih.gov/pubmed/21283610
http://dx.doi.org/10.1371/journal.pntd.0000947
_version_ 1782197077486338048
author Li, Ben-Wen
Rush, Amy C.
Jiang, Dao-Jun
Mitreva, Makedonka
Abubucker, Sahar
Weil, Gary J.
author_facet Li, Ben-Wen
Rush, Amy C.
Jiang, Dao-Jun
Mitreva, Makedonka
Abubucker, Sahar
Weil, Gary J.
author_sort Li, Ben-Wen
collection PubMed
description BACKGROUND: A better understanding of reproductive processes in parasitic nematodes may lead to development of new anthelmintics and control strategies for combating disabling and disfiguring neglected tropical diseases such as lymphatic filariasis and onchocerciasis. Transcriptomatic analysis has provided important new insights into mechanisms of reproduction and development in other invertebrates. We have performed the first genome-wide analysis of gender-associated (GA) gene expression in a filarial nematode to improve understanding of key reproductive processes in these parasites. METHODOLOGY/PRINCIPAL FINDINGS: The Version 2 Filarial Microarray with 18,104 elements representing ∼85% of the filarial genome was used to identify GA gene transcripts in adult Brugia malayi worms. Approximately 19% of 14,293 genes were identified as GA genes. Many GA genes have potential Caenorhabditis elegans homologues annotated as germline-, oogenesis-, spermatogenesis-, and early embryogenesis- enriched. The potential C. elegans homologues of the filarial GA genes have a higher frequency of severe RNAi phenotypes (such as lethal and sterility) than other C. elegans genes. Molecular functions and biological processes associated with GA genes were gender-segregated. Peptidase, ligase, transferase, regulator activity for kinase and transcription, and rRNA and lipid binding were associated with female GA genes. In contrast, catalytic activity from kinase, ATP, and carbohydrate binding were associated with male GA genes. Cell cycle, transcription, translation, and biological regulation were increased in females, whereas metabolic processes of phosphate and carbohydrate metabolism, energy generation, and cell communication were increased in males. Significantly enriched pathways in females were associated with cell growth and protein synthesis, whereas metabolic pathways such as pentose phosphate and energy production pathways were enriched in males. There were also striking gender differences in environmental information processing and cell communication pathways. Many proteins encoded by GA genes are secreted by Brugia malayi, and these encode immunomodulatory molecules such as antioxidants and host cytokine mimics. Expression of many GA genes has been recently reported to be suppressed by tetracycline, which blocks reproduction in female Brugia malayi. Our localization of GA transcripts in filarial reproductive organs supports the hypothesis that these genes encode proteins involved in reproduction. CONCLUSIONS/SIGNIFICANCE: Genome-wide expression profiling coupled with a robust bioinformatics analysis has greatly expanded our understanding of the molecular biology of reproduction in filarial nematodes. This study has highlighted key molecules and pathways associated with reproductive and other biological processes and identified numerous potential candidates for rational drug design to target reproductive processes.
format Text
id pubmed-3026763
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-30267632011-01-31 Gender-Associated Genes in Filarial Nematodes Are Important for Reproduction and Potential Intervention Targets Li, Ben-Wen Rush, Amy C. Jiang, Dao-Jun Mitreva, Makedonka Abubucker, Sahar Weil, Gary J. PLoS Negl Trop Dis Research Article BACKGROUND: A better understanding of reproductive processes in parasitic nematodes may lead to development of new anthelmintics and control strategies for combating disabling and disfiguring neglected tropical diseases such as lymphatic filariasis and onchocerciasis. Transcriptomatic analysis has provided important new insights into mechanisms of reproduction and development in other invertebrates. We have performed the first genome-wide analysis of gender-associated (GA) gene expression in a filarial nematode to improve understanding of key reproductive processes in these parasites. METHODOLOGY/PRINCIPAL FINDINGS: The Version 2 Filarial Microarray with 18,104 elements representing ∼85% of the filarial genome was used to identify GA gene transcripts in adult Brugia malayi worms. Approximately 19% of 14,293 genes were identified as GA genes. Many GA genes have potential Caenorhabditis elegans homologues annotated as germline-, oogenesis-, spermatogenesis-, and early embryogenesis- enriched. The potential C. elegans homologues of the filarial GA genes have a higher frequency of severe RNAi phenotypes (such as lethal and sterility) than other C. elegans genes. Molecular functions and biological processes associated with GA genes were gender-segregated. Peptidase, ligase, transferase, regulator activity for kinase and transcription, and rRNA and lipid binding were associated with female GA genes. In contrast, catalytic activity from kinase, ATP, and carbohydrate binding were associated with male GA genes. Cell cycle, transcription, translation, and biological regulation were increased in females, whereas metabolic processes of phosphate and carbohydrate metabolism, energy generation, and cell communication were increased in males. Significantly enriched pathways in females were associated with cell growth and protein synthesis, whereas metabolic pathways such as pentose phosphate and energy production pathways were enriched in males. There were also striking gender differences in environmental information processing and cell communication pathways. Many proteins encoded by GA genes are secreted by Brugia malayi, and these encode immunomodulatory molecules such as antioxidants and host cytokine mimics. Expression of many GA genes has been recently reported to be suppressed by tetracycline, which blocks reproduction in female Brugia malayi. Our localization of GA transcripts in filarial reproductive organs supports the hypothesis that these genes encode proteins involved in reproduction. CONCLUSIONS/SIGNIFICANCE: Genome-wide expression profiling coupled with a robust bioinformatics analysis has greatly expanded our understanding of the molecular biology of reproduction in filarial nematodes. This study has highlighted key molecules and pathways associated with reproductive and other biological processes and identified numerous potential candidates for rational drug design to target reproductive processes. Public Library of Science 2011-01-25 /pmc/articles/PMC3026763/ /pubmed/21283610 http://dx.doi.org/10.1371/journal.pntd.0000947 Text en Li 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Li, Ben-Wen
Rush, Amy C.
Jiang, Dao-Jun
Mitreva, Makedonka
Abubucker, Sahar
Weil, Gary J.
Gender-Associated Genes in Filarial Nematodes Are Important for Reproduction and Potential Intervention Targets
title Gender-Associated Genes in Filarial Nematodes Are Important for Reproduction and Potential Intervention Targets
title_full Gender-Associated Genes in Filarial Nematodes Are Important for Reproduction and Potential Intervention Targets
title_fullStr Gender-Associated Genes in Filarial Nematodes Are Important for Reproduction and Potential Intervention Targets
title_full_unstemmed Gender-Associated Genes in Filarial Nematodes Are Important for Reproduction and Potential Intervention Targets
title_short Gender-Associated Genes in Filarial Nematodes Are Important for Reproduction and Potential Intervention Targets
title_sort gender-associated genes in filarial nematodes are important for reproduction and potential intervention targets
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3026763/
https://www.ncbi.nlm.nih.gov/pubmed/21283610
http://dx.doi.org/10.1371/journal.pntd.0000947
work_keys_str_mv AT libenwen genderassociatedgenesinfilarialnematodesareimportantforreproductionandpotentialinterventiontargets
AT rushamyc genderassociatedgenesinfilarialnematodesareimportantforreproductionandpotentialinterventiontargets
AT jiangdaojun genderassociatedgenesinfilarialnematodesareimportantforreproductionandpotentialinterventiontargets
AT mitrevamakedonka genderassociatedgenesinfilarialnematodesareimportantforreproductionandpotentialinterventiontargets
AT abubuckersahar genderassociatedgenesinfilarialnematodesareimportantforreproductionandpotentialinterventiontargets
AT weilgaryj genderassociatedgenesinfilarialnematodesareimportantforreproductionandpotentialinterventiontargets