DNA-synthesis in larval salivary glands during culture in starved female flies of Drosophila melanogaster.

K Weber, R Nöthiger
{"title":"DNA-synthesis in larval salivary glands during culture in starved female flies of Drosophila melanogaster.","authors":"K Weber,&nbsp;R Nöthiger","doi":"10.1007/BF00575320","DOIUrl":null,"url":null,"abstract":"<p><p>If imaginal disks are transplanted into host flies that are kept on a protein-free sugar diet, their developmental processes come to a more or less reversibel standstill. This block is generally attributed to absence of cell divisions. Since cell division and DNA-synthesis are intimately coupled, we have used the polytene system of the salivary glands in order to study the question whether DNA-synthesis is possible in starved hosts.Nuclear DNA was determined with a modified Feulgen technique using the fluorescent dye BAO. Salivary glands of 72 hrs old male larvae were cultured in vivo and in vitro under various conditions (Fig. 2, Table 2, 3). In young starved hosts the nuclei can complete an already initiated S-phase, but further synthesis is blocked (Figs. 4, 5, 6). Older starved hosts are more effective in blocking DNA-synthesis. This block is largely reversible: in hosts that are transferred onto complete yeast food, the nuclei resume DNA-synthesis at a normal rate (Table 2, Kg. 5). Cytoplasmic differentiation as indicated by vacuolization of cultured gland cells has also been shown to be reversibly blocked in starved hosts (Fig. 7). Contrary to these findings starvation seemed to cause some irreversible alterations at the chromosomal level (Fig. 8).We suggest that in starved hosts protein synthesis is blocked and that this in turn will prevent initiation of new S-phases.</p>","PeriodicalId":54406,"journal":{"name":"Wilhelm Roux Archiv Fur Entwicklungsmechanik Der Organismen","volume":"176 4","pages":"253-266"},"PeriodicalIF":0.0000,"publicationDate":"1975-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/BF00575320","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Wilhelm Roux Archiv Fur Entwicklungsmechanik Der Organismen","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/BF00575320","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

If imaginal disks are transplanted into host flies that are kept on a protein-free sugar diet, their developmental processes come to a more or less reversibel standstill. This block is generally attributed to absence of cell divisions. Since cell division and DNA-synthesis are intimately coupled, we have used the polytene system of the salivary glands in order to study the question whether DNA-synthesis is possible in starved hosts.Nuclear DNA was determined with a modified Feulgen technique using the fluorescent dye BAO. Salivary glands of 72 hrs old male larvae were cultured in vivo and in vitro under various conditions (Fig. 2, Table 2, 3). In young starved hosts the nuclei can complete an already initiated S-phase, but further synthesis is blocked (Figs. 4, 5, 6). Older starved hosts are more effective in blocking DNA-synthesis. This block is largely reversible: in hosts that are transferred onto complete yeast food, the nuclei resume DNA-synthesis at a normal rate (Table 2, Kg. 5). Cytoplasmic differentiation as indicated by vacuolization of cultured gland cells has also been shown to be reversibly blocked in starved hosts (Fig. 7). Contrary to these findings starvation seemed to cause some irreversible alterations at the chromosomal level (Fig. 8).We suggest that in starved hosts protein synthesis is blocked and that this in turn will prevent initiation of new S-phases.

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
饥饿黑腹果蝇雌蝇培养过程中幼虫唾液腺的dna合成。
如果将想象磁盘移植到不含蛋白质的糖饮食的宿主果蝇体内,它们的发育过程就会进入一个或多或少可逆的停滞状态。这种阻滞通常归因于细胞分裂的缺失。由于细胞分裂和dna合成是密切耦合的,我们利用唾液腺的多烯系统来研究饥饿宿主是否可能进行dna合成。核DNA采用改良Feulgen技术,荧光染料BAO测定。在体内和体外不同条件下培养72小时龄雄性幼虫的唾液腺(图2、表2、3)。在饥饿的年轻宿主中,细胞核可以完成已经启动的s期,但进一步的合成被阻断(图4、5、6)。年龄较大的饥饿宿主更有效地阻断dna合成。这个块很大程度上是可逆的:在被转移到完全酵母食物的宿主中,细胞核以正常速率恢复dna合成(表2;通过培养的腺体细胞空泡化所显示的细胞质分化也被证明在饥饿的宿主中被可逆地阻断(图7)。与这些发现相反,饥饿似乎在染色体水平上引起了一些不可逆的改变(图8)。我们认为,在饥饿的宿主中,蛋白质合成被阻断,这反过来又会阻止新的s期的开始。
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 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
DNA-synthesis in larval salivary glands during culture in starved female flies of Drosophila melanogaster. [Growth and regeneration of the eye of the larvae ofAeshna cyanea Müll. (Odonata, Anisoptera)]. [Further data on the roles of skin and internal tissues in limb regeneration of the newtPleurodeles waltlii Michah. (Amphibia Urodela)]. [Regeneration of X-irradiated limbs ofPleurodeles waltlii Michah. (Urodele). The influence of quality and orientation of non irradiated grafts]. Purification and partial characterization of an actin-like protein from cricket early egg plasmodium.
×
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