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果蝇后极质的移植。卵前极生殖细胞的诱导。

Transplantation of posterior polar plasm in Drosophila. Induction of germ cells at the anterior pole of the egg.

作者信息

Illmensee K, Mahowald A P

出版信息

Proc Natl Acad Sci U S A. 1974 Apr;71(4):1016-20. doi: 10.1073/pnas.71.4.1016.

DOI:10.1073/pnas.71.4.1016
PMID:4208545
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC388152/
Abstract

In Drosophila melanogaster the primordial germ cells are normally formed at the posterior tip of the egg during the preblastoderm stage. In order to determine whether the posterior polar plasm is capable of inducing the formation of primordial germ cells in another region of the embryo, portions of this cytoplasm were transferred from wild-type embryos of the early cleavage stage to the anterior tip of mwh e embryos of the same age. At various times after the injection (15-200 min), embryos were fixed for histological analysis. Alternating thick and thin sections were examined for the presence of experimentally induced pole cells. In more than half of the embryos analyzed in this way, one to six cells were found containing the polar granules as well as round nuclear structures, both of which are characteristic of normal pole cells and are not present in blastoderm cells. In order to determine whether these "pole cells" function normally, i.e., develop further into germ cells, the cells induced at the anterior tip of mwh e blastoderm embryos were introduced into the posterior region of y w sn(3) hosts of the same age. The flies resulting from these embryos were mated to y w sn(3) partners. In addition to the expected y w sn(3) progeny, wild-type flies heterozygous for mwh e and, therefore, descended from the experimentally induced pole cells were found in 4% of the crosses. Such flies did not appear in the control experiments after transfer of normal anterior cells from noninjected blastoderm embryos. These results demonstrate that the posterior polar plasm can be transferred to the anterior tip of the embryo and that in this presumptive somatic region it still retains its capacity to determine the formation of the primordial germ cells.

摘要

在黑腹果蝇中,原始生殖细胞通常在胚盘形成前期于卵的后端形成。为了确定后端极质是否能够在胚胎的其他区域诱导原始生殖细胞的形成,将该细胞质的部分从早期卵裂阶段的野生型胚胎转移到同龄的mwh e胚胎的前端。在注射后的不同时间(15 - 200分钟),将胚胎固定用于组织学分析。检查交替的厚切片和薄切片中是否存在实验诱导的极细胞。以这种方式分析的超过一半的胚胎中,发现有一到六个细胞含有极颗粒以及圆形核结构,这两者都是正常极细胞的特征,而在胚盘细胞中不存在。为了确定这些“极细胞”是否正常发挥功能,即是否进一步发育成生殖细胞,将在mwh e胚盘胚胎前端诱导的细胞引入同龄的yw sn(3)宿主的后端区域。由这些胚胎产生的果蝇与yw sn(3)的果蝇交配。除了预期的yw sn(3)后代外,在4%的杂交中发现了杂合mwh e的野生型果蝇,因此它们是由实验诱导的极细胞发育而来的。在从未注射的胚盘胚胎转移正常前端细胞后的对照实验中没有出现这样的果蝇。这些结果表明,后端极质可以转移到胚胎的前端,并且在这个假定的体细胞区域它仍然保留着决定原始生殖细胞形成的能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f126/388152/bba367f4539f/pnas00057-0012-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f126/388152/bba367f4539f/pnas00057-0012-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f126/388152/bba367f4539f/pnas00057-0012-a.jpg

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