Evidence from ileum and liver transcriptomes of resistance to high-salt and water-deprivation conditions in camel.

IF 1.7 3区 生物学 Q2 ZOOLOGY
Zoological Letters Pub Date : 2020-06-05 eCollection Date: 2020-01-01 DOI:10.1186/s40851-020-00159-3
Dong Zhang, Jing Pan, Huanmin Zhou, Yu Cao
{"title":"Evidence from ileum and liver transcriptomes of resistance to high-salt and water-deprivation conditions in camel.","authors":"Dong Zhang,&nbsp;Jing Pan,&nbsp;Huanmin Zhou,&nbsp;Yu Cao","doi":"10.1186/s40851-020-00159-3","DOIUrl":null,"url":null,"abstract":"<p><p>Camels have evolved various resistance characteristics adaptive to their desert habitats. In the present study, we used high-throughput sequencing to investigate stress-induced alternative splicing events as well as different genes involved in resistance to water deprivation and salt absorption in the ileum and liver in <i>Camelus bactrianus</i>. Through association analyses of mRNA, miRNA and lncRNA, we sought to explicate how camels respond to high salt and water scarcity conditions. There were two modes by which genes driven by alternative splicing were enriched to molecular functions, invoking of which was potentially fixed by organ and stress types. With qRT-PCR detection, the differentially expressed <i>MUC6</i>, <i>AQP5</i>, <i>LOC105076960</i>, <i>PKP4</i>, <i>CDH11</i>, <i>TENM1, SDS</i>, <i>LOC105061856</i>, <i>PLIN2</i> and <i>UPP2</i> were screened as functionally important genes, along with miR-29b, miR-484, miR-362-5p, miR-96, miR-195, miR-128 and miR-148a. These genes contributed to cellular stress resistance, for instance by reducing water loss, inhibiting excessive import of sodium, improving protective barriers and sodium ion homeostasis, and maintaining uridine content. The underlying competing endogenous RNAs referred to LNC001664, let-7e and <i>LOC105076960</i> mRNA in ileum, and LNC001438, LNC003417, LNC001770, miR-199c and <i>TENM1</i> mRNA in liver. Besides competent interpretation to resistance, there may be inspirations for curing human diseases triggered by high-salt intake.</p>","PeriodicalId":54280,"journal":{"name":"Zoological Letters","volume":"6 ","pages":"8"},"PeriodicalIF":1.7000,"publicationDate":"2020-06-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/s40851-020-00159-3","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Zoological Letters","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1186/s40851-020-00159-3","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2020/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"ZOOLOGY","Score":null,"Total":0}
引用次数: 2

Abstract

Camels have evolved various resistance characteristics adaptive to their desert habitats. In the present study, we used high-throughput sequencing to investigate stress-induced alternative splicing events as well as different genes involved in resistance to water deprivation and salt absorption in the ileum and liver in Camelus bactrianus. Through association analyses of mRNA, miRNA and lncRNA, we sought to explicate how camels respond to high salt and water scarcity conditions. There were two modes by which genes driven by alternative splicing were enriched to molecular functions, invoking of which was potentially fixed by organ and stress types. With qRT-PCR detection, the differentially expressed MUC6, AQP5, LOC105076960, PKP4, CDH11, TENM1, SDS, LOC105061856, PLIN2 and UPP2 were screened as functionally important genes, along with miR-29b, miR-484, miR-362-5p, miR-96, miR-195, miR-128 and miR-148a. These genes contributed to cellular stress resistance, for instance by reducing water loss, inhibiting excessive import of sodium, improving protective barriers and sodium ion homeostasis, and maintaining uridine content. The underlying competing endogenous RNAs referred to LNC001664, let-7e and LOC105076960 mRNA in ileum, and LNC001438, LNC003417, LNC001770, miR-199c and TENM1 mRNA in liver. Besides competent interpretation to resistance, there may be inspirations for curing human diseases triggered by high-salt intake.

Abstract Image

Abstract Image

Abstract Image

来自回肠和肝脏转录组对骆驼高盐和缺水条件的抗性的证据。
骆驼已经进化出适应沙漠栖息地的各种抵抗特性。在本研究中,我们利用高通量测序技术研究了驼鹿(Camelus bactrianus)回肠和肝脏中应激诱导的选择性剪接事件以及参与抵抗水分剥夺和盐吸收的不同基因。通过mRNA、miRNA和lncRNA的关联分析,我们试图解释骆驼对高盐和缺水条件的反应。由选择性剪接驱动的基因通过两种模式被富集为分子功能,其调用可能被器官和应激类型所固定。通过qRT-PCR检测,筛选差异表达MUC6、AQP5、LOC105076960、PKP4、CDH11、TENM1、SDS、LOC105061856、PLIN2和UPP2为功能重要基因,以及miR-29b、miR-484、miR-362-5p、miR-96、miR-195、miR-128和miR-148a。这些基因有助于细胞抗逆性,例如通过减少水分流失,抑制钠的过度进口,改善保护屏障和钠离子稳态,以及维持尿苷含量。潜在的竞争内源性rna包括回肠中的LNC001664、let-7e和LOC105076960 mRNA,肝脏中的LNC001438、LNC003417、LNC001770、miR-199c和TENM1 mRNA。除了对耐药性的合理解释外,这可能对治疗高盐摄入引发的人类疾病有启发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Zoological Letters
Zoological Letters Agricultural and Biological Sciences-Animal Science and Zoology
CiteScore
3.60
自引率
0.00%
发文量
12
审稿时长
10 weeks
期刊介绍: Zoological Letters is an open access journal that publishes new and important findings in the zoological sciences. As a sister journal to Zoological Science, Zoological Letters covers a wide range of basic fields of zoology, from taxonomy to bioinformatics. We also welcome submissions of paleontology reports as part of our effort to contribute to the development of new perspectives in evolutionary zoology. Our goal is to serve as a global publishing forum for fundamental researchers in all fields of zoology.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信