Cargando…

A novel laminin β gene BmLanB1-w regulates wing-specific cell adhesion in silkworm, Bombyx mori

Laminins are important basement membrane (BM) components with crucial roles in development. The numbers of laminin isoforms in various organisms are determined by the composition of the different α, β, and γ chains, and their coding genes, which are variable across spieces. In insects, only two α, o...

Descripción completa

Detalles Bibliográficos
Autores principales: Tong, Xiaoling, He, Songzhen, Chen, Jun, Hu, Hai, Xiang, Zhonghuai, Lu, Cheng, Dai, Fangyin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4515764/
https://www.ncbi.nlm.nih.gov/pubmed/26212529
http://dx.doi.org/10.1038/srep12562
_version_ 1782382969128747008
author Tong, Xiaoling
He, Songzhen
Chen, Jun
Hu, Hai
Xiang, Zhonghuai
Lu, Cheng
Dai, Fangyin
author_facet Tong, Xiaoling
He, Songzhen
Chen, Jun
Hu, Hai
Xiang, Zhonghuai
Lu, Cheng
Dai, Fangyin
author_sort Tong, Xiaoling
collection PubMed
description Laminins are important basement membrane (BM) components with crucial roles in development. The numbers of laminin isoforms in various organisms are determined by the composition of the different α, β, and γ chains, and their coding genes, which are variable across spieces. In insects, only two α, one β, and one γ chains have been identified thus far. Here, we isolated a novel laminin β gene, BmLanB1-w, by positional cloning of the mutant (crayfish, cf) with blistered wings in silkworm. Gene structure analysis showed that a 2 bp deletion of the BmLanB1-w gene in the cf mutant caused a frame-shift in the open reading frame (ORF) and generated a premature stop codon. Knockdown of the BmLanB1-w gene produced individuals exhibiting blistered wings, indicating that this laminin gene was required for cell adhesion during wing development. We also identified laminin homologs in different species and showed that two copies of β laminin likely originated in Lepidoptera during evolution. Furthermore, phylogenetic and gene expression analyses of silkworm laminin genes revealed that the BmLanB1-w gene is newly evolved, and is required for wing-specific cell adhesion. This is the first report showing the tissue specific distribution and functional differentiation of β laminin in insects.
format Online
Article
Text
id pubmed-4515764
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-45157642015-07-29 A novel laminin β gene BmLanB1-w regulates wing-specific cell adhesion in silkworm, Bombyx mori Tong, Xiaoling He, Songzhen Chen, Jun Hu, Hai Xiang, Zhonghuai Lu, Cheng Dai, Fangyin Sci Rep Article Laminins are important basement membrane (BM) components with crucial roles in development. The numbers of laminin isoforms in various organisms are determined by the composition of the different α, β, and γ chains, and their coding genes, which are variable across spieces. In insects, only two α, one β, and one γ chains have been identified thus far. Here, we isolated a novel laminin β gene, BmLanB1-w, by positional cloning of the mutant (crayfish, cf) with blistered wings in silkworm. Gene structure analysis showed that a 2 bp deletion of the BmLanB1-w gene in the cf mutant caused a frame-shift in the open reading frame (ORF) and generated a premature stop codon. Knockdown of the BmLanB1-w gene produced individuals exhibiting blistered wings, indicating that this laminin gene was required for cell adhesion during wing development. We also identified laminin homologs in different species and showed that two copies of β laminin likely originated in Lepidoptera during evolution. Furthermore, phylogenetic and gene expression analyses of silkworm laminin genes revealed that the BmLanB1-w gene is newly evolved, and is required for wing-specific cell adhesion. This is the first report showing the tissue specific distribution and functional differentiation of β laminin in insects. Nature Publishing Group 2015-07-27 /pmc/articles/PMC4515764/ /pubmed/26212529 http://dx.doi.org/10.1038/srep12562 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Tong, Xiaoling
He, Songzhen
Chen, Jun
Hu, Hai
Xiang, Zhonghuai
Lu, Cheng
Dai, Fangyin
A novel laminin β gene BmLanB1-w regulates wing-specific cell adhesion in silkworm, Bombyx mori
title A novel laminin β gene BmLanB1-w regulates wing-specific cell adhesion in silkworm, Bombyx mori
title_full A novel laminin β gene BmLanB1-w regulates wing-specific cell adhesion in silkworm, Bombyx mori
title_fullStr A novel laminin β gene BmLanB1-w regulates wing-specific cell adhesion in silkworm, Bombyx mori
title_full_unstemmed A novel laminin β gene BmLanB1-w regulates wing-specific cell adhesion in silkworm, Bombyx mori
title_short A novel laminin β gene BmLanB1-w regulates wing-specific cell adhesion in silkworm, Bombyx mori
title_sort novel laminin β gene bmlanb1-w regulates wing-specific cell adhesion in silkworm, bombyx mori
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4515764/
https://www.ncbi.nlm.nih.gov/pubmed/26212529
http://dx.doi.org/10.1038/srep12562
work_keys_str_mv AT tongxiaoling anovellamininbgenebmlanb1wregulateswingspecificcelladhesioninsilkwormbombyxmori
AT hesongzhen anovellamininbgenebmlanb1wregulateswingspecificcelladhesioninsilkwormbombyxmori
AT chenjun anovellamininbgenebmlanb1wregulateswingspecificcelladhesioninsilkwormbombyxmori
AT huhai anovellamininbgenebmlanb1wregulateswingspecificcelladhesioninsilkwormbombyxmori
AT xiangzhonghuai anovellamininbgenebmlanb1wregulateswingspecificcelladhesioninsilkwormbombyxmori
AT lucheng anovellamininbgenebmlanb1wregulateswingspecificcelladhesioninsilkwormbombyxmori
AT daifangyin anovellamininbgenebmlanb1wregulateswingspecificcelladhesioninsilkwormbombyxmori
AT tongxiaoling novellamininbgenebmlanb1wregulateswingspecificcelladhesioninsilkwormbombyxmori
AT hesongzhen novellamininbgenebmlanb1wregulateswingspecificcelladhesioninsilkwormbombyxmori
AT chenjun novellamininbgenebmlanb1wregulateswingspecificcelladhesioninsilkwormbombyxmori
AT huhai novellamininbgenebmlanb1wregulateswingspecificcelladhesioninsilkwormbombyxmori
AT xiangzhonghuai novellamininbgenebmlanb1wregulateswingspecificcelladhesioninsilkwormbombyxmori
AT lucheng novellamininbgenebmlanb1wregulateswingspecificcelladhesioninsilkwormbombyxmori
AT daifangyin novellamininbgenebmlanb1wregulateswingspecificcelladhesioninsilkwormbombyxmori