首页> 外文期刊>BMC Genomics >Identifying specific proteins involved in eggshell membrane formation using gene expression analysis and bioinformatics
【24h】

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

机译:使用基因表达分析和生物信息学鉴定参与蛋壳膜形成的特定蛋白质

获取原文
获取外文期刊封面目录资料

摘要

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. 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. 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.
机译:禽蛋壳膜围绕蛋清,为蛋壳钙化提供了结构基础,这对于禽类繁殖至关重要。此外,它还是具有许多潜在工业和生物医学应用的天然生物材料。由于蛋壳膜纤维的不溶性和稳定性,它们的形成和蛋白质成分仍然很难鉴定。这项研究的目的是通过分析输卵管白色峡部区段的转录组来鉴定编码蛋壳膜蛋白的基因,特别是那些负责其结构特征的基因,该部位是负责制造膜纤维的专门区域。使用Del-Mar 14?K鸡微阵列研究与母猪输卵管相邻的大酒瓶(Ma)和子宫(Ut)区段相比,白色峡部(WI)转录本的上调表达。分析表明有135个克隆与过量表达的转录本(WI / Ma ++ WI / Ut)杂交,并对应于107个NCBI注释的非冗余鸡胚基因ID。这项综合分析表明,在白色峡部中高度过量表达的结构蛋白包括胶原蛋白X(COL10A1),原纤维蛋白1(FBN1)和富含半胱氨酸的蛋壳膜蛋白(CREMP)。这些结果验证了先前的蛋白质组学研究,这些研究已经确定了可溶性蛋壳提取物中的胶原蛋白X(α-1)和CREMP。编码胶原加工酶的基因,如赖氨酰氧化酶同源物1、2和3(LOXL1,LOXL2和LOXL3),脯氨酰4羟化酶亚基α-2和β多肽(P4HA2和P4HB)以及肽基脯氨酰顺反异构酶C (PPIC)也被过度表达。此外,鉴定了编码已知调节二硫键交联的蛋白质的基因,包括巯基氧化酶(QSOX1)和硫氧还蛋白(TXN),这表明白色峡部中基因的协同上调与蛋壳膜纤维的形成有关。本研究确定了与白色峡部卵壳膜形成过程中胶原蛋白,其他结构蛋白的加工以及二硫键介导的交联相关的基因。这些基因的鉴定将提供蛋壳膜结构和形成机理的新见识,这将有助于选择策略的发展,以提高蛋壳质量和食用鸡蛋的食品安全性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号