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      Identifying specific proteins involved in eggshell membrane formation using gene expression analysis and bioinformatics

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          Abstract

          Background

          The avian eggshell membranes surround the egg white and provide a structural foundation for calcification of the eggshell which is essential for avian reproduction; moreover, it is also a natural biomaterial with many potential industrial and biomedical applications. Due to the insoluble and stable nature of the eggshell membrane fibres, their formation and protein constituents remain poorly characterized. The purpose of this study was to identify genes encoding eggshell membrane proteins, particularly those responsible for its structural features, by analyzing the transcriptome of the white isthmus segment of the oviduct, which is the specialized region responsible for the fabrication of the membrane fibres.

          Results

          The Del-Mar 14 K chicken microarray was used to investigate up-regulated expression of transcripts in the white isthmus (WI) compared with the adjacent magnum (Ma) and uterine (Ut) segments of the hen oviduct. Analysis revealed 135 clones hybridizing to over-expressed transcripts (WI/Ma + WI/Ut), and corresponding to 107 NCBI annotated non-redundant Gallus gallus gene IDs. This combined analysis revealed that the structural proteins highly over-expressed in the white isthmus include collagen X ( COL10A1), fibrillin-1 ( FBN1) and cysteine rich eggshell membrane protein ( CREMP). These results validate previous proteomics studies which have identified collagen X (α-1) and CREMP in soluble eggshell extracts. Genes encoding collagen-processing enzymes such as lysyl oxidase homologs 1, 2 and 3 ( LOXL1, LOXL2 and LOXL3), prolyl 4 hydroxylase subunit α-2 and beta polypeptide ( P4HA2 and P4HB) as well as peptidyl-prolyl cis-trans isomerase C ( PPIC) were also over-expressed. Additionally, genes encoding proteins known to regulate disulfide cross-linking, including sulfhydryl oxidase ( QSOX1) and thioredoxin ( TXN), were identified which suggests that coordinated up-regulation of genes in the white isthmus is associated with eggshell membrane fibre formation.

          Conclusions

          The present study has identified genes associated with the processing of collagen, other structural proteins, and disulfide-mediated cross-linking during eggshell membrane formation in the white isthmus. Identification of these genes will provide new insight into eggshell membrane structure and mechanisms of formation that will assist in the development of selection strategies to improve eggshell quality and food safety of the table egg.

          Electronic supplementary material

          The online version of this article (doi:10.1186/s12864-015-2013-3) contains supplementary material, which is available to authorized users.

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          Most cited references69

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          Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing

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            Thioredoxin and glutaredoxin systems.

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              The TDRD9-MIWI2 complex is essential for piRNA-mediated retrotransposon silencing in the mouse male germline.

              Host-defense mechanisms against transposable elements are critical to protect the genome information. Here we show that tudor-domain containing 9 (Tdrd9) is essential for silencing Line-1 retrotransposon in the mouse male germline. Tdrd9 encodes an ATPase/DExH-type helicase, and its mutation causes male sterility showing meiotic failure. In Tdrd9 mutants, Line-1 was highly activated and piwi-interacting small RNAs (piRNAs) corresponding to Line-1 were increased, suggesting that feedforward amplification operates in the mutant. In fetal testes, Tdrd9 mutation causes Line-1 desilencing and an aberrant piRNA profile in prospermatogonia, followed by cognate DNA demethylation. TDRD9 complexes with MIWI2 with distinct compartmentalization in processing bodies, and this TDRD9-MIWI2 localization is regulated by MILI and TDRD1 residing at intermitochondrial cement. Our results identify TDRD9 as a functional partner of MIWI2 and indicate that the tudor-piwi association is a conserved feature, while two separate axes, TDRD9-MIWI2 and TDRD1-MILI, cooperate nonredundantly in the piwi-small RNA pathway in the mouse male germline. 2009 Elsevier Inc. All rights reserved.
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                Author and article information

                Contributors
                jdu013@uottawa.ca
                mhincke@uottawa.ca
                mrose025@uottawa.ca
                christelle.hennequet@tours.inra.fr
                aurelien.brionne@tours.inra.fr
                cogburn@udel.edu
                yves.nys@tours.inra.fr
                joel.gautron@tours.inra.fr
                Journal
                BMC Genomics
                BMC Genomics
                BMC Genomics
                BioMed Central (London )
                1471-2164
                15 October 2015
                15 October 2015
                2015
                : 16
                : 792
                Affiliations
                [ ]Department of Cellular and Molecular Medicine, University of Ottawa, 451 Smyth Road, Ottawa, K1H 8 M5, Canada
                [ ]INRA, UR83 Recherches Avicoles, F-37380, Nouzilly, France
                [ ]Department of Animal and Food Sciences, University of Delaware, Newark, DE 19717 USA
                Article
                2013
                10.1186/s12864-015-2013-3
                4608100
                26470705
                4ed06237-565e-466f-b725-eacb7891e049
                © Du et al. 2015

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 31 July 2015
                : 4 October 2015
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2015

                Genetics
                chicken eggshell membrane,white isthmus,collagens,bioinformatics,transcriptome
                Genetics
                chicken eggshell membrane, white isthmus, collagens, bioinformatics, transcriptome

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