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Golden orb-weaving spider (Trichonephila clavipes) silk genes with sex-biased expression and atypical architectures

Spider silks are renowned for their high-performance mechanical properties. Contributing to these properties are proteins encoded by the spidroin (spider fibroin) gene family. Spidroins have been discovered mostly through cDNA studies of females based on the presence of conserved terminal regions an...

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Autores principales: Correa-Garhwal, Sandra M, Babb, Paul L, Voight, Benjamin F, Hayashi, Cheryl Y
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8022711/
https://www.ncbi.nlm.nih.gov/pubmed/33561241
http://dx.doi.org/10.1093/g3journal/jkaa039
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author Correa-Garhwal, Sandra M
Babb, Paul L
Voight, Benjamin F
Hayashi, Cheryl Y
author_facet Correa-Garhwal, Sandra M
Babb, Paul L
Voight, Benjamin F
Hayashi, Cheryl Y
author_sort Correa-Garhwal, Sandra M
collection PubMed
description Spider silks are renowned for their high-performance mechanical properties. Contributing to these properties are proteins encoded by the spidroin (spider fibroin) gene family. Spidroins have been discovered mostly through cDNA studies of females based on the presence of conserved terminal regions and a repetitive central region. Recently, genome sequencing of the golden orb-web weaver, Trichonephila clavipes, provided a complete picture of spidroin diversity. Here, we refine the annotation of T. clavipes spidroin genes including the reclassification of some as non-spidroins. We rename these non-spidroins as spidroin-like (SpL) genes because they have repetitive sequences and amino acid compositions like spidroins, but entirely lack the archetypal terminal domains of spidroins. Insight into the function of these spidroin and SpL genes was then examined through tissue- and sex-specific gene expression studies. Using qPCR, we show that some silk genes are upregulated in male silk glands compared to females, despite males producing less silk in general. We also find that an enigmatic spidroin that lacks a spidroin C-terminal domain is highly expressed in silk glands, suggesting that spidroins could assemble into fibers without a canonical terminal region. Further, we show that two SpL genes are expressed in silk glands, with one gene highly evolutionarily conserved across species, providing evidence that particular SpL genes are important to silk production. Together, these findings challenge long-standing paradigms regarding the evolutionary and functional significance of the proteins and conserved motifs essential for producing spider silks.
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spelling pubmed-80227112021-04-09 Golden orb-weaving spider (Trichonephila clavipes) silk genes with sex-biased expression and atypical architectures Correa-Garhwal, Sandra M Babb, Paul L Voight, Benjamin F Hayashi, Cheryl Y G3 (Bethesda) Investigation Spider silks are renowned for their high-performance mechanical properties. Contributing to these properties are proteins encoded by the spidroin (spider fibroin) gene family. Spidroins have been discovered mostly through cDNA studies of females based on the presence of conserved terminal regions and a repetitive central region. Recently, genome sequencing of the golden orb-web weaver, Trichonephila clavipes, provided a complete picture of spidroin diversity. Here, we refine the annotation of T. clavipes spidroin genes including the reclassification of some as non-spidroins. We rename these non-spidroins as spidroin-like (SpL) genes because they have repetitive sequences and amino acid compositions like spidroins, but entirely lack the archetypal terminal domains of spidroins. Insight into the function of these spidroin and SpL genes was then examined through tissue- and sex-specific gene expression studies. Using qPCR, we show that some silk genes are upregulated in male silk glands compared to females, despite males producing less silk in general. We also find that an enigmatic spidroin that lacks a spidroin C-terminal domain is highly expressed in silk glands, suggesting that spidroins could assemble into fibers without a canonical terminal region. Further, we show that two SpL genes are expressed in silk glands, with one gene highly evolutionarily conserved across species, providing evidence that particular SpL genes are important to silk production. Together, these findings challenge long-standing paradigms regarding the evolutionary and functional significance of the proteins and conserved motifs essential for producing spider silks. Oxford University Press 2020-12-22 /pmc/articles/PMC8022711/ /pubmed/33561241 http://dx.doi.org/10.1093/g3journal/jkaa039 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of Genetics Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Investigation
Correa-Garhwal, Sandra M
Babb, Paul L
Voight, Benjamin F
Hayashi, Cheryl Y
Golden orb-weaving spider (Trichonephila clavipes) silk genes with sex-biased expression and atypical architectures
title Golden orb-weaving spider (Trichonephila clavipes) silk genes with sex-biased expression and atypical architectures
title_full Golden orb-weaving spider (Trichonephila clavipes) silk genes with sex-biased expression and atypical architectures
title_fullStr Golden orb-weaving spider (Trichonephila clavipes) silk genes with sex-biased expression and atypical architectures
title_full_unstemmed Golden orb-weaving spider (Trichonephila clavipes) silk genes with sex-biased expression and atypical architectures
title_short Golden orb-weaving spider (Trichonephila clavipes) silk genes with sex-biased expression and atypical architectures
title_sort golden orb-weaving spider (trichonephila clavipes) silk genes with sex-biased expression and atypical architectures
topic Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8022711/
https://www.ncbi.nlm.nih.gov/pubmed/33561241
http://dx.doi.org/10.1093/g3journal/jkaa039
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