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在饥饿的黑腹果蝇雌性幼虫唾液腺培养过程中的DNA合成。

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

作者信息

Weber K, Nöthiger R

机构信息

Zoological Institute, University of Zurich, Switzerland.

出版信息

Wilhelm Roux Arch Entwickl Mech Org. 1975 Dec;176(4):253-266. doi: 10.1007/BF00575320.

DOI:10.1007/BF00575320
PMID:28304982
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.

摘要

如果将成虫盘移植到以无糖蛋白质饲料饲养的宿主果蝇中,其发育过程或多或少会进入一个可逆的停滞状态。这种阻滞通常归因于细胞分裂的缺失。由于细胞分裂与DNA合成密切相关,我们利用唾液腺的多线系统来研究在饥饿宿主中DNA合成是否可能。使用荧光染料BAO的改良孚尔根技术测定核DNA。在各种条件下对72小时龄雄性幼虫的唾液腺进行体内和体外培养(图2,表2、3)。在年轻的饥饿宿主中,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在阻断DNA合成方面更有效。这种阻滞在很大程度上是可逆的:在转移到完整酵母食物上的宿主中,细胞核以正常速率恢复DNA合成(表2,图5)。培养的腺细胞空泡化所表明细胞质分化在饥饿宿主中也被证明是可逆阻滞的(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变化(图8)。我们认为在饥饿宿主中蛋白质合成被阻断,而这反过来又会阻止新S期的启动。

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引用本文的文献

1
Developmental potentials of the cells of the male foreleg disc ofDrosophila : I. Pattern regulation in intact fragments.果蝇雄性前腿盘细胞的发育潜能:I. 完整片段中的模式调控
Wilehm Roux Arch Dev Biol. 1977 Dec;181(4):309-320. doi: 10.1007/BF00848058.

本文引用的文献

1
Histotypic reaggregation of dissociated imaginal disc cells ofDrosophila melanogaster culturedin vivo.在体内培养的黑腹果蝇解离成虫盘细胞的组织型重聚集。
Wilhelm Roux Arch Entwickl Mech Org. 1967 Sep;158(3):212-217. doi: 10.1007/BF00573398.
2
[On the DNA content of salivary gland nuclei with "full-grown" giant chromosomes in Drosophila melanogaster].[关于黑腹果蝇中具有“成熟”巨型染色体的唾液腺细胞核的DNA含量]
Experientia. 1964 Oct 15;20(10):566-7. doi: 10.1007/BF02150295.
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[Developmental capacity of embryonal blastema in Drosophila following cultivation in an adult host].
[成年宿主培养后果蝇胚胎芽基的发育能力]
Rev Suisse Zool. 1968 Sep;75(3):557-69.
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Non replicating DNA in Drosophila.果蝇中的非复制性DNA。
Genetics. 1969;61(1):Suppl:227-38.
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[Synthesis processes at the gaint chromosomes of Glyptotendipes].[雕翅摇蚊巨大染色体的合成过程]
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Chromosomes isolated from unfixed salivary gland of Chironomus.从摇蚊未固定的唾液腺中分离出的染色体。
Results Probl Cell Differ. 1972;4:35-57. doi: 10.1007/978-3-540-37164-9_2.
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Differentiation of transplanted larval salivary glands of Drosophila hydei in adults of the same species.
J Exp Zool. 1965 Dec;160(3):299-317. doi: 10.1002/jez.1401600308.
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Regeneration of Drosophila melanogaster male leg disc fragments in sugar fed female hosts.黑腹果蝇雄性腿部盘状碎片在喂食糖的雌性宿主体内的再生
Experientia. 1973 May 15;29(5):631-2. doi: 10.1007/BF01926712.
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Replication in polytene chromosomes.多线染色体中的复制。
Results Probl Cell Differ. 1972;4:59-85. doi: 10.1007/978-3-540-37164-9_3.
10
DNA replication in salivary gland nuclei of Drosophila melanogaster at successive larval and prepupal stages.黑腹果蝇在幼虫和蛹前期连续阶段唾液腺细胞核中的DNA复制。
Genetics. 1967 Mar;55(3):375-86. doi: 10.1093/genetics/55.3.375.