The expansion of genes encoding soluble silk components in the greater wax moth, Galleria mellonella
Language English Country England, Great Britain Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
30448349
DOI
10.1016/j.ibmb.2018.11.003
PII: S0965-1748(18)30383-7
Knihovny.cz E-resources
- Keywords
- B. mori, Cocoon, Lepidoptera, Mucin, Sericin, Silk glands,
- MeSH
- Phylogeny MeSH
- Glycoproteins chemistry genetics metabolism MeSH
- Silk genetics metabolism MeSH
- Insect Proteins chemistry genetics metabolism MeSH
- Larva genetics growth & development metabolism MeSH
- Mucins chemistry genetics metabolism MeSH
- Moths genetics growth & development metabolism MeSH
- Proteome * MeSH
- Amino Acid Sequence MeSH
- Base Sequence MeSH
- Sequence Alignment MeSH
- Sericins chemistry genetics metabolism MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Glycoproteins MeSH
- Silk MeSH
- Insect Proteins MeSH
- Mucins MeSH
- Proteome * MeSH
- Sericins MeSH
Lepidopteran silk is a complex assembly of proteins produced by a pair of highly specialized labial glands called silk glands. Silk composition has been examined only in a handful of species. Here we report on the analysis of silk gland-specific transcriptomes from three developmental stages of the greater wax moth, Galleria mellonella, combined with proteomics, Edman microsequencing and northern blot analysis. In addition to the genes known earlier, we identified twenty seven candidate cDNAs predicted to encode secretory proteins, which may represent novel silk components. Eight were verified by proteomic analysis or microsequencing, and several others were confirmed by similarity with known silk genes and their expression patterns. Our results revealed that most candidates encode abundant secreted proteins produced by middle silk glands including ten sericins, two seroins, one or more mucins, and several sequences without apparent similarity to known proteins. We did not detect any novel PSG-specific protein, confirming that there are only three fibroin subunits. Our data not only show that the number of sericin genes in the greater wax moth is higher than in other species thus far examined, but also the total content of soluble proteins in silk is twice as high in G. mellonella than in B. mori or A. yamamai. Our data will serve as a foundation for future identification and evolutionary analysis of silk proteins in the Lepidoptera.
Faculty of Science University of South Bohemia Branisovska 31 370 05 Ceske Budejovice Czech Republic
References provided by Crossref.org
Characterization and comparative analysis of sericin protein 150 in Bombyx mori
Using the multi-omics approach to reveal the silk composition in Plectrocnemia conspersa