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通过注射来自卵的亚细胞级分诱导灭菌果蝇胚胎的极细胞。

Induction of pole cells in sterilized Drosophila embryos by injection of subcellular fraction from eggs.

机构信息

Institute of Biological Sciences, University of Tsukuba, Sakura-mura, Ibaraki 305, Japan.

出版信息

Proc Natl Acad Sci U S A. 1982 Nov;79(22):6946-50. doi: 10.1073/pnas.79.22.6946.

DOI:10.1073/pnas.79.22.6946
PMID:16593252
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC347251/
Abstract

A subcellular fraction isolated from a homogenate of young Drosophila embryos was shown to be capable of inducing pole cells when injected into UV-sterilized Drosophila embryos. Most of the pole cell-inducing activity was recovered from the precipitate after centrifugation at 27,000 x g. The activity remained in this precipitate (called F-3 fraction hereafter) even after membranous structures were removed from it through centrifugation on a sucrose density gradient. Dialysis, lyophilization, and heating at 80 degrees C for 10 min did not inactivate the F-3 fraction. The pole cells, which were produced when the F-3 fraction was injected at the posterior pole of UV-sterilized embryos, did not develop into germ cells. Furthermore, the F-3 fraction was unable to induce pole cells when injected into the anterior region of the egg. These results can be explained by assuming that (i) pole cell formation and germ cell determination are controlled by different factors, (ii) pole cell formation requires at least two factors, which are normally localized in the posterior-pole cytoplasm, one of which is sensitive and one resistant to the UV dosage we used, and (iii) the subcellular fraction we obtained contains the UV-sensitive factor but not the UV-resistant factor.

摘要

从年轻果蝇胚胎匀浆中分离出的亚细胞级分被证明能够在注射到紫外线灭菌的果蝇胚胎中诱导极细胞。大多数极细胞诱导活性从 27000xg 离心后的沉淀物中回收。即使通过在蔗糖密度梯度上离心去除膜结构,该活性仍保留在该沉淀物中(以下称为 F-3 级分)。透析、冻干和在 80°C 加热 10 分钟不会使 F-3 级分失活。当将 F-3 级分注射到紫外线灭菌胚胎的后极时,产生的极细胞不会发育成生殖细胞。此外,当将 F-3 级分注射到卵的前区域时,它不能诱导极细胞。这些结果可以通过以下假设来解释:(i)极细胞形成和生殖细胞决定由不同的因素控制,(ii)极细胞形成至少需要两种因子,这些因子通常位于后极细胞质中,其中一种对我们使用的紫外线剂量敏感,另一种则有抗性,(iii)我们获得的亚细胞级分包含紫外线敏感因子而不包含紫外线抗性因子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fc8/347251/8da4354413a5/pnas00461-0219-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fc8/347251/e54c748c899b/pnas00461-0218-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fc8/347251/8da4354413a5/pnas00461-0219-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fc8/347251/e54c748c899b/pnas00461-0218-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fc8/347251/8da4354413a5/pnas00461-0219-a.jpg

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本文引用的文献

1
Certain aspects of cell lineage and morphogenesis studied in embryos of Drosophila melanogaster with an ultra-violet micro-beam.利用紫外线微束对黑腹果蝇胚胎中的细胞谱系和形态发生的某些方面进行了研究。
J Embryol Exp Morphol. 1961 Jun;9:310-25.
2
Developmental fate of pole cells in Drosophila melanogaster.黑腹果蝇极细胞的发育命运
Dev Biol. 1980 Jun 15;77(2):303-14. doi: 10.1016/0012-1606(80)90476-5.
3
Experimental studies on the role of 'polar granules' in the segregation of pole cells in Drosophila melanogaster.关于“极颗粒”在黑腹果蝇极细胞分离中作用的实验研究。
J Embryol Exp Morphol. 1966 Dec;16(3):391-9.
4
Experiments on chromosome elimination in the gall midge, Mayetiola destructor.对麦红吸浆虫(Mayetiola destructor)染色体消除的实验。
J Embryol Exp Morphol. 1970 Sep;24(2):257-86.
5
Determination of blastoderm cells in Drosophila melanogaster.黑腹果蝇中胚盘细胞的测定
Proc Natl Acad Sci U S A. 1971 Sep;68(9):2217-21. doi: 10.1073/pnas.68.9.2217.
6
Nuclear transplantation in Drosophila melanogaster.黑腹果蝇中的核移植
Nature. 1971 Mar 19;230(5290):185-6. doi: 10.1038/230185a0.
7
A low-viscosity epoxy resin embedding medium for electron microscopy.一种用于电子显微镜的低粘度环氧树脂包埋介质。
J Ultrastruct Res. 1969 Jan;26(1):31-43. doi: 10.1016/s0022-5320(69)90033-1.
8
Transplantation of posterior polar plasm in Drosophila. Induction of germ cells at the anterior pole of the egg.果蝇后极质的移植。卵前极生殖细胞的诱导。
Proc Natl Acad Sci U S A. 1974 Apr;71(4):1016-20. doi: 10.1073/pnas.71.4.1016.
9
Restoration of fertility in sterilized Drosophila eggs by transplantation of polar cytoplasm.通过移植极细胞质恢复绝育果蝇卵的生育能力。
Dev Biol. 1974 Mar;37(1):43-54. doi: 10.1016/0012-1606(74)90168-7.
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Polar granules of drosophila. IV. Cytochemical studies showing loss of RNA from polar granules during early stages of embryogenesis.果蝇的极颗粒。IV. 细胞化学研究表明在胚胎发生早期极颗粒中RNA的丧失。
J Exp Zool. 1971 Mar;176(3):345-52. doi: 10.1002/jez.1401760309.