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The genomic underpinnings of apoptosis in the silkworm, Bombyx mori

BACKGROUND: Apoptosis is regulated in an orderly fashion by a series of genes, and has a crucial role in important physiological processes such as growth development, immunological response and so on. Recently, substantial studies have been undertaken on apoptosis in model animals including humans,...

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Autores principales: Zhang, Jin-Ye, Pan, Min-Hui, Sun, Zhi-Ya, Huang, Shu-Jing, Yu, Zi-Shu, Liu, Di, Zhao, Dan-Hong, Lu, Cheng
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3091752/
https://www.ncbi.nlm.nih.gov/pubmed/21040523
http://dx.doi.org/10.1186/1471-2164-11-611
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author Zhang, Jin-Ye
Pan, Min-Hui
Sun, Zhi-Ya
Huang, Shu-Jing
Yu, Zi-Shu
Liu, Di
Zhao, Dan-Hong
Lu, Cheng
author_facet Zhang, Jin-Ye
Pan, Min-Hui
Sun, Zhi-Ya
Huang, Shu-Jing
Yu, Zi-Shu
Liu, Di
Zhao, Dan-Hong
Lu, Cheng
author_sort Zhang, Jin-Ye
collection PubMed
description BACKGROUND: Apoptosis is regulated in an orderly fashion by a series of genes, and has a crucial role in important physiological processes such as growth development, immunological response and so on. Recently, substantial studies have been undertaken on apoptosis in model animals including humans, fruit flies, and the nematode. However, the lack of genomic data for silkworms limits their usefulness in apoptosis studies, despite the advantages of silkworm as a representative of Lepidoptera and an effective model system. Herein we have identified apoptosis-related genes in the silkworm Bombyx mori and compared them to those from insects, mammals, and nematodes. RESULTS: From the newly assembled genome databases, a genome-wide analysis of apoptosis-related genes in Bombyx mori was performed using both nucleotide and protein Blast searches. Fifty-two apoptosis-related candidate genes were identified, including five caspase family members, two tumor necrosis factor (TNF) superfamily members, one Bcl-2 family member, four baculovirus IAP (inhibitor of apoptosis) repeat (BIR) domain family members and 1 RHG (Reaper, Hid, Grim, and Sickle; Drosophila cell death activators) family member. Moreover, we identified a new caspase family member, BmCaspase-New, two splice variants of BmDronc, and Bm3585, a mammalian TNF superfamily member homolog. Twenty-three of these apoptosis-related genes were cloned and sequenced using cDNA templates isolated from BmE-SWU1 cells. Sequence analyses revealed that these genes could have key roles in apoptosis. CONCLUSIONS: Bombyx mori possesses potential apoptosis-related genes. We hypothesized that the classic intrinsic and extrinsic apoptotic pathways potentially are active in Bombyx mori. These results lay the foundation for further apoptosis-related study in Bombyx mori.
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spelling pubmed-30917522011-05-11 The genomic underpinnings of apoptosis in the silkworm, Bombyx mori Zhang, Jin-Ye Pan, Min-Hui Sun, Zhi-Ya Huang, Shu-Jing Yu, Zi-Shu Liu, Di Zhao, Dan-Hong Lu, Cheng BMC Genomics Research Article BACKGROUND: Apoptosis is regulated in an orderly fashion by a series of genes, and has a crucial role in important physiological processes such as growth development, immunological response and so on. Recently, substantial studies have been undertaken on apoptosis in model animals including humans, fruit flies, and the nematode. However, the lack of genomic data for silkworms limits their usefulness in apoptosis studies, despite the advantages of silkworm as a representative of Lepidoptera and an effective model system. Herein we have identified apoptosis-related genes in the silkworm Bombyx mori and compared them to those from insects, mammals, and nematodes. RESULTS: From the newly assembled genome databases, a genome-wide analysis of apoptosis-related genes in Bombyx mori was performed using both nucleotide and protein Blast searches. Fifty-two apoptosis-related candidate genes were identified, including five caspase family members, two tumor necrosis factor (TNF) superfamily members, one Bcl-2 family member, four baculovirus IAP (inhibitor of apoptosis) repeat (BIR) domain family members and 1 RHG (Reaper, Hid, Grim, and Sickle; Drosophila cell death activators) family member. Moreover, we identified a new caspase family member, BmCaspase-New, two splice variants of BmDronc, and Bm3585, a mammalian TNF superfamily member homolog. Twenty-three of these apoptosis-related genes were cloned and sequenced using cDNA templates isolated from BmE-SWU1 cells. Sequence analyses revealed that these genes could have key roles in apoptosis. CONCLUSIONS: Bombyx mori possesses potential apoptosis-related genes. We hypothesized that the classic intrinsic and extrinsic apoptotic pathways potentially are active in Bombyx mori. These results lay the foundation for further apoptosis-related study in Bombyx mori. BioMed Central 2010-10-31 /pmc/articles/PMC3091752/ /pubmed/21040523 http://dx.doi.org/10.1186/1471-2164-11-611 Text en Copyright ©2010 Zhang et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zhang, Jin-Ye
Pan, Min-Hui
Sun, Zhi-Ya
Huang, Shu-Jing
Yu, Zi-Shu
Liu, Di
Zhao, Dan-Hong
Lu, Cheng
The genomic underpinnings of apoptosis in the silkworm, Bombyx mori
title The genomic underpinnings of apoptosis in the silkworm, Bombyx mori
title_full The genomic underpinnings of apoptosis in the silkworm, Bombyx mori
title_fullStr The genomic underpinnings of apoptosis in the silkworm, Bombyx mori
title_full_unstemmed The genomic underpinnings of apoptosis in the silkworm, Bombyx mori
title_short The genomic underpinnings of apoptosis in the silkworm, Bombyx mori
title_sort genomic underpinnings of apoptosis in the silkworm, bombyx mori
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3091752/
https://www.ncbi.nlm.nih.gov/pubmed/21040523
http://dx.doi.org/10.1186/1471-2164-11-611
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