Surani M A, Barton S C, Howlett S K, Norris M L
Department of Molecular Embryology, Institute of Animal Physiology and Genetics Research, Cambridge, UK.
Development. 1988 May;103(1):171-8.
We have examined the role of germline-specific chromosomal determinants of development in the mouse. Studies were carried out using aggregation chimaeras between androgenetic----fertilized embryos and compared with similar parthenogenetic----fertilized chimaeras. Several adult chimaeras were found with parthenogenetic cells but none were found with androgenetic cells. Analysis of chimaeras at mid-gestation showed that parthenogenetic cells were detected in the embryo and yolk sac but that androgenetic cells were found only in the trophoblast and yolk sac and not in the embryo. The contribution of parthenogenetic cells to the embryo and yolk sac was increased by aggregating 2-cell parthenogenetic and 4-cell fertilized embryos but the contribution of parthenogenetic cells in extraembryonic tissues remained negligible even after aggregation of 4-cell parthenogenetic and 2-cell fertilized embryos. Furthermore, parthenogenetic cells were primarily found in the yolk sac mesoderm and not in the yolk sac endoderm. These results suggest that maternal chromosomes in parthenogenetic cells permit their participation in the primitive ectoderm lineage but these cells are presumably eliminated by selective pressure or autonomous cell lethality from the primitive endoderm and trophectoderm lineages. Conversely paternal chromosomes in androgenetic cells confer opposite properties since the embryonic cells can be detected in the trophoblast and the yolk sac but not in the embryos, presumably because they are eliminated from the primitive ectoderm lineage. The spatial distribution of cells with different parental chromosomes may occur partly because of differential expression of some genes, such as proto-oncogenes, and partly due to their ability to respond to a variety of diffusible growth factors.
我们研究了小鼠发育过程中种系特异性染色体决定因素的作用。使用孤雄受精胚胎之间的聚合嵌合体进行研究,并与类似的孤雌受精嵌合体进行比较。发现几只成年嵌合体含有孤雌生殖细胞,但没有发现含有孤雄生殖细胞的嵌合体。对妊娠中期嵌合体的分析表明,在胚胎和卵黄囊中检测到了孤雌生殖细胞,但孤雄生殖细胞仅在滋养层和卵黄囊中发现,而不在胚胎中。通过将2细胞孤雌生殖胚胎和4细胞受精胚胎聚集在一起,孤雌生殖细胞对胚胎和卵黄囊的贡献增加了,但即使在4细胞孤雌生殖胚胎和2细胞受精胚胎聚集后,孤雌生殖细胞在胚外组织中的贡献仍然可以忽略不计。此外,孤雌生殖细胞主要存在于卵黄囊的中胚层,而不是卵黄囊的内胚层。这些结果表明,孤雌生殖细胞中的母源染色体允许它们参与原始外胚层谱系,但这些细胞可能由于选择压力或自主细胞致死性而从原始内胚层和滋养外胚层谱系中被消除。相反,孤雄生殖细胞中的父源染色体赋予相反的特性,因为胚胎细胞可以在滋养层和卵黄囊中检测到,但在胚胎中没有,推测是因为它们从原始外胚层谱系中被消除。具有不同亲本染色体的细胞的空间分布可能部分是由于某些基因(如原癌基因)的差异表达,部分是由于它们对多种可扩散生长因子的反应能力。