• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

RACK1 调控出芽被囊动物有性和无性繁殖过程中的间质细胞募集。

RACK1 regulates mesenchymal cell recruitment during sexual and asexual reproduction of budding tunicates.

机构信息

Laboratory of Cellular and Molecular Biotechnology, Faculty of Science, Kochi University, Kochi 780-8520, Japan.

出版信息

Dev Biol. 2012 Aug 15;368(2):393-403. doi: 10.1016/j.ydbio.2012.06.006. Epub 2012 Jun 12.

DOI:10.1016/j.ydbio.2012.06.006
PMID:22698545
Abstract

A homolog of receptor for activated protein kinase C1 (RACK1) was cloned from the budding tunicate Polyandrocarpa misakiensis. By RT-PCR and in situ hybridization analyses, PmRACK1 showed biphasic gene expression during asexual and sexual reproduction. In developing buds, the signal was exclusively observed in the multipotent atrial epithelium and undifferentiated mesenchymal cells that contributed to morphogenesis by the mesenchymal-epithelial transition (MET). In juvenile zooids, the signal was first observable in germline precursor cells that arose as mesenchymal cell aggregated in the ventral hemocoel. In mature zooids, the germinal epithelium in the ovary and the pharynx were the most heavily stained parts. GFP reporter assay indicated that the ovarian expression of PmRACK1 was constitutive from germline precursor cells to oocytes. To elucidate the in vivo function of PmRACK1, RNA interference was challenged. When growing buds were incubated with 5 nmol/mL siRNA, most mesenchymal cells remained round and appeared to have no interactions with the extracellular matrix (ECM), causing lower activity of MET without any apparent effects on cell proliferation. The resultant zooids became growth-deficient. The dwarf zooids did not form buds or mature gonads. Prior to RNAi, buds were treated with human BMP4 that could induce PmRACK1 expression, which resulted in MET activity. We conclude that in P. misakiensis, PmRACK1 plays roles in mesenchymal cell recruitment during formation of somatic and gonad tissues, which contributes to zooidal growth and sexual and asexual reproduction.

摘要

从芽胞被囊动物多瘤海鞘 Polyandrocarpa misakiensis 中克隆出了激活蛋白激酶 C1 受体(RACK1)的同源物。通过 RT-PCR 和原位杂交分析,PmRACK1 在无性和有性生殖过程中表现出两相基因表达。在发育中的芽中,信号仅在多能性心房上皮细胞和未分化的间充质细胞中观察到,这些细胞通过间质-上皮转化(MET)为形态发生做出贡献。在幼体浮游生物中,信号首先在生殖细胞前体细胞中观察到,这些细胞是在腹侧血腔中聚集的间充质细胞产生的。在成熟的浮游生物中,卵巢和咽部的生殖上皮是染色最深的部分。GFP 报告基因分析表明,PmRACK1 的卵巢表达从生殖细胞前体细胞到卵母细胞是组成型的。为了阐明 PmRACK1 的体内功能,进行了 RNA 干扰挑战。当生长的芽与 5 nmol/mL siRNA 孵育时,大多数间充质细胞保持圆形,似乎与细胞外基质(ECM)没有相互作用,导致 MET 活性降低,而对细胞增殖没有任何明显影响。由此产生的浮游生物生长不足。矮小的浮游生物不能形成芽或成熟的性腺。在 RNAi 之前,用人类 BMP4 处理芽,BMP4 可以诱导 PmRACK1 的表达,从而导致 MET 活性。我们得出结论,在多瘤海鞘中,PmRACK1 在形成体细胞和性腺组织的间充质细胞募集中发挥作用,这有助于浮游生物的生长和有性和无性繁殖。

相似文献

1
RACK1 regulates mesenchymal cell recruitment during sexual and asexual reproduction of budding tunicates.RACK1 调控出芽被囊动物有性和无性繁殖过程中的间质细胞募集。
Dev Biol. 2012 Aug 15;368(2):393-403. doi: 10.1016/j.ydbio.2012.06.006. Epub 2012 Jun 12.
2
Involvement of vasa homolog in germline recruitment from coelomic stem cells in budding tunicates.血管同源物在出芽被囊动物中从体腔干细胞募集生殖细胞过程中的作用。
Dev Genes Evol. 2007 Jan;217(1):1-11. doi: 10.1007/s00427-006-0112-5. Epub 2006 Oct 17.
3
Senescence-associated superoxide dismutase influences mitochondrial gene expression in budding tunicates.衰老相关的超氧化物歧化酶影响芽胞动物的线粒体基因表达。
Dev Growth Differ. 2013 Jun;55(5):606-14. doi: 10.1111/dgd.12065. Epub 2013 May 16.
4
Expression and function of myc during asexual reproduction of the budding ascidian Polyandrocarpa misakiensis.在芽生海鞘 Polyandrocarpa misakiensis 的无性生殖过程中 myc 的表达和功能。
Dev Growth Differ. 2011 Dec;53(9):1004-14. doi: 10.1111/j.1440-169X.2011.01312.x.
5
Molecular anatomy of tunicate senescence: reversible function of mitochondrial and nuclear genes associated with budding cycles.被囊动物衰老的分子解剖学:与出芽周期相关的线粒体和核基因的可逆功能。
Development. 2012 Nov;139(21):4083-93. doi: 10.1242/dev.083170. Epub 2012 Sep 26.
6
The transcription factor AP2 and downstream genes shared by asexual reproduction and zooidal regeneration in the tunicate, Polyandrocarpa misakiensis.转录因子AP2以及被海鞘三崎聚雄海鞘无性繁殖和个体再生所共享的下游基因。
Cells Dev. 2024 Mar;177:203885. doi: 10.1016/j.cdev.2023.203885. Epub 2023 Nov 23.
7
Role of Vasa, Piwi, and Myc-expressing coelomic cells in gonad regeneration of the colonial tunicate, Botryllus primigenus.腔肠细胞中 Vasa、Piwi 和 Myc 表达细胞在原始被囊动物(Botryllus primigenus)性腺再生中的作用。
Mech Dev. 2011 Sep-Dec;128(7-10):457-70. doi: 10.1016/j.mod.2011.09.001. Epub 2011 Sep 10.
8
Expression and function of a retinoic acid receptor in budding ascidians.
Dev Genes Evol. 1998 Dec;208(10):537-46. doi: 10.1007/s004270050213.
9
A retinoic acid-inducible modular protease in budding ascidians.芽殖海鞘中一种视黄酸诱导的模块化蛋白酶。
Dev Biol. 1999 Oct 1;214(1):38-45. doi: 10.1006/dbio.1999.9400.
10
Cell adhesion in the process of asexual reproduction of tunicates.
Microsc Res Tech. 1999 Feb 15;44(4):269-78. doi: 10.1002/(SICI)1097-0029(19990215)44:4<269::AID-JEMT6>3.0.CO;2-K.

引用本文的文献

1
A microRNA Cluster-Lefty Pathway is Required for Cellulose Synthesis During Ascidian Larval Metamorphosis.海鞘幼虫变态过程中纤维素合成需要一个微小RNA簇-Lefty信号通路。
Front Cell Dev Biol. 2022 Mar 15;10:835906. doi: 10.3389/fcell.2022.835906. eCollection 2022.
2
A pan-metazoan concept for adult stem cells: the wobbling Penrose landscape.泛动物门成体干细胞概念:摇摆的彭罗斯景观。
Biol Rev Camb Philos Soc. 2022 Feb;97(1):299-325. doi: 10.1111/brv.12801. Epub 2021 Oct 6.
3
YAF2-Mediated YY1-Sirtuin6 Interactions Responsible for Mitochondrial Downregulation in Aging Tunicates.
YAF2 介导的 YY1-Sirtuin6 相互作用负责衰老被囊动物中线粒体的下调。
Mol Cell Biol. 2021 Jun 23;41(7):e0004721. doi: 10.1128/MCB.00047-21.
4
Novel budding mode in : a model for comparative studies on asexual development and whole body regeneration.新型出芽模式:无性发育和全身再生比较研究的模型
Evodevo. 2019 Apr 3;10:7. doi: 10.1186/s13227-019-0121-x. eCollection 2019.