mED2-A参与小鼠胚胎发育的新基因

DUAN Jia-Zhong , ZHANG Jing-Pu , ZHU Shao-Xia
{"title":"mED2-A参与小鼠胚胎发育的新基因","authors":"DUAN Jia-Zhong ,&nbsp;ZHANG Jing-Pu ,&nbsp;ZHU Shao-Xia","doi":"10.1016/S0379-4172(06)60101-7","DOIUrl":null,"url":null,"abstract":"<div><p>Dissection of new genes underlying embryonic development is important for our understanding of the molecular mechanism of vertebrate embryonic development. In this study, the expression pattern and functional analysis of a new gene, called <em>mED2</em>, originally cloned from mouse embryos using subtractive hybridization was reported. <em>mED2</em> expression patterns were characterized by RT-PCR-Southern hybridization and <em>in situ</em> hybridization. The results showed that <em>mED2</em> was mainly expressed in the embryonic nervous system and mesoderm-derived tissues and its expression varied depending on the embryonic developmental stages. The knockdown of <em>mED2</em> activity by antisense RNA injection inhibited zygote cleavage and blastocyst formation during pre-implantation in mice. Subcellular localization of mED2-eGFP fusion protein revealed a pattern of nuclear membrane and juxta-/perinuclear location such as in the rough endoplasmic reticulum and Golgi apparatus. This finding was supported by bioinformatics analysis, which indicated mED2 protein to be a transmembrane protein with partial homology to the thioredoxin family of proteins. It is inferred that <em>mED2</em> gene can probably take part in early embryonic development in mouse and may be involved in target protein posttranslational modification, turnover, folding, and stability at the endoplasmic reticulum and/or the Golgi apparatus.</p></div>","PeriodicalId":100017,"journal":{"name":"Acta Genetica Sinica","volume":"33 8","pages":"Pages 692-701"},"PeriodicalIF":0.0000,"publicationDate":"2006-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0379-4172(06)60101-7","citationCount":"3","resultStr":"{\"title\":\"mED2—A Novel Gene Involved in Mouse Embryonic Development\",\"authors\":\"DUAN Jia-Zhong ,&nbsp;ZHANG Jing-Pu ,&nbsp;ZHU Shao-Xia\",\"doi\":\"10.1016/S0379-4172(06)60101-7\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Dissection of new genes underlying embryonic development is important for our understanding of the molecular mechanism of vertebrate embryonic development. In this study, the expression pattern and functional analysis of a new gene, called <em>mED2</em>, originally cloned from mouse embryos using subtractive hybridization was reported. <em>mED2</em> expression patterns were characterized by RT-PCR-Southern hybridization and <em>in situ</em> hybridization. The results showed that <em>mED2</em> was mainly expressed in the embryonic nervous system and mesoderm-derived tissues and its expression varied depending on the embryonic developmental stages. The knockdown of <em>mED2</em> activity by antisense RNA injection inhibited zygote cleavage and blastocyst formation during pre-implantation in mice. Subcellular localization of mED2-eGFP fusion protein revealed a pattern of nuclear membrane and juxta-/perinuclear location such as in the rough endoplasmic reticulum and Golgi apparatus. This finding was supported by bioinformatics analysis, which indicated mED2 protein to be a transmembrane protein with partial homology to the thioredoxin family of proteins. It is inferred that <em>mED2</em> gene can probably take part in early embryonic development in mouse and may be involved in target protein posttranslational modification, turnover, folding, and stability at the endoplasmic reticulum and/or the Golgi apparatus.</p></div>\",\"PeriodicalId\":100017,\"journal\":{\"name\":\"Acta Genetica Sinica\",\"volume\":\"33 8\",\"pages\":\"Pages 692-701\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2006-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/S0379-4172(06)60101-7\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Acta Genetica Sinica\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0379417206601017\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta Genetica Sinica","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0379417206601017","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 3

摘要

解剖胚胎发育的新基因对我们理解脊椎动物胚胎发育的分子机制非常重要。在这项研究中,报道了一个新的基因,称为mED2的表达模式和功能分析,最初是用减法杂交从小鼠胚胎中克隆出来的。通过RT-PCR-Southern杂交和原位杂交对mED2的表达模式进行了表征。结果表明,mED2主要表达于胚胎神经系统和中胚层组织中,其表达随胚胎发育阶段的不同而不同。注射反义RNA抑制mED2活性抑制小鼠着床前受精卵裂解和囊胚形成。mED2-eGFP融合蛋白的亚细胞定位揭示了核膜和核旁/核周定位的模式,如粗内质网和高尔基体。这一发现得到了生物信息学分析的支持,表明mED2蛋白是一个跨膜蛋白,与硫氧还蛋白家族部分同源。推测mED2基因可能参与小鼠早期胚胎发育,并可能参与靶蛋白在内质网和/或高尔基体的翻译后修饰、翻转、折叠和稳定性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
mED2—A Novel Gene Involved in Mouse Embryonic Development

Dissection of new genes underlying embryonic development is important for our understanding of the molecular mechanism of vertebrate embryonic development. In this study, the expression pattern and functional analysis of a new gene, called mED2, originally cloned from mouse embryos using subtractive hybridization was reported. mED2 expression patterns were characterized by RT-PCR-Southern hybridization and in situ hybridization. The results showed that mED2 was mainly expressed in the embryonic nervous system and mesoderm-derived tissues and its expression varied depending on the embryonic developmental stages. The knockdown of mED2 activity by antisense RNA injection inhibited zygote cleavage and blastocyst formation during pre-implantation in mice. Subcellular localization of mED2-eGFP fusion protein revealed a pattern of nuclear membrane and juxta-/perinuclear location such as in the rough endoplasmic reticulum and Golgi apparatus. This finding was supported by bioinformatics analysis, which indicated mED2 protein to be a transmembrane protein with partial homology to the thioredoxin family of proteins. It is inferred that mED2 gene can probably take part in early embryonic development in mouse and may be involved in target protein posttranslational modification, turnover, folding, and stability at the endoplasmic reticulum and/or the Golgi apparatus.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Ultrastructure and Gene Mapping of the Albino Mutant al12 in Rice (Oryza sativa L.) Differential Expression of Endogenous Ferritin Genes and Iron Homeostasis Alteration in Transgenic Tobacco Overexpressing Soybean Ferritin Gene Analysis of the Phylogenetic Relationships Among Several Species of Gramineae Using ACGM Markers Powers of Multiple-Testing Procedures for Identification of Genes Significantly Differentially Expressed in Microarray Experiments Fluorescent Multiplex Amplification of Three X-STR Loci
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1