THE GENETIC-CONTROL AND GERM-CELL KINETICS OF THE FEMALE AND MALE GERM LINE IN MAMMALS INCLUDING MAN

被引:37
作者
HILSCHER, W
机构
[1] Department of Experimental Pathology, Medical Institute for Environmental Hygiene at the Heinrich-Heine, University of Düsseldorf, D-4000 Düsseldorf
关键词
GERM LINE (KEIMBAHN); OOGENICPRESPERMATOGENIC WAVE; SPERMATOGENIC SYSTEM; OOCYTE; EMBRYO TRANSGENIC ANIMALS;
D O I
10.1093/oxfordjournals.humrep.a137281
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
The female germ line (germ cell lineage, Keimbahn) is provided with only one proliferation wave, the oogenic, whereas male gametogenesis involves two successive waves: prespermatogenic, which corresponds to the female proliferation wave, and spermatogenesis, which is responsible for the immense number of male gametes produced in mature testes. Both male proliferation systems are linked by the transitional or T prospermatogonia. Using the reverse percentage of labelled metaphases method, it has been shown that the first differences between female and male germ cells can be identified by the end of the first wave, when oogonia and multiplying or M prospermatogonia are proliferating. This prenatal first wave of proliferation of male germ cells was also demonstrated in man and ceases around the 22nd week of pregnancy. Spermatogenesis involves a stock of stem cells (stem spermatogonia), a flexibly reacting pool of undifferentiated spermatogonia and several generations of differentiating spermatogonia, which proliferate almost exponentially. Furthermore, it consists of spermatocytes and haploid spermatids transforming into spermatozoa. The oocytes pass through the preleptotene stage, synthesizing DNA, and thereafter traverse the meiotic prophase up to the diplotene stage. In mammals they act as 'pre-embryos' in a similar but to a lesser degree than oocytes of amphibia and insects. The maternal chromosomes are largely responsible for the development of the embryo, the paternal genome for the development of the extra-embryonic tissue. The synthesis of transgenic animals is a powerful weapon in the armoury of geneticists, as has recently been demonstrated: a 14 kb genomic DNA fragment (Sry) is sufficient to induce testis differentiation and subsequent male development when introduced into chromosomally female mouse embryos.
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收藏
页码:1416 / 1425
页数:10
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共 125 条
[101]  
Redi C.A., Hilscher B., Winking H., Stage-dependent enzymatic activities in spermatogenesis of mice with the standard karyotype and chromosomal variants with impaired fertility, Andrology, 15, pp. 322-330, (1983)
[102]  
Redi C.A., Garagna S., Mazzini G., Winking H., Pericen-tromeric hcicrochromatin and AT contents during Robertsonian fusion in the house mouse, Chromosome, 13, pp. 31-35, (1986)
[103]  
Redi C.A., Hilscher B., Winking H., Unscheduled labelling by 3H-thymidinc in mouse pachytene spermatocytes and round spermatids of Robertsonian translocation carriers, Cell. Mol. Biol., 34, pp. 149-156, (1988)
[104]  
Roosen-Runge E.C., Germinal-cell loss in normal metaznan spermatogenesis, J. Reprod. Fertil, 35, pp. 339-348, (1973)
[105]  
Sawicki J.A., Magnuson T., Epstein C.J., Evidence for expression of the paternal genome in the two-cell mouse embryo, Nature, 294, pp. 450-451, (1981)
[106]  
Schultz R.M., Lctoumeau G.E., Wassarman P.M., Program of early development in the mammal: Changes in the pattern and absolute rates of tubulin and total protein synthesis during oocyte growth in the mouse. Dev, Biol, 73, pp. 120-133, (1979)
[107]  
Schwochau G., Haider S.G., Anat. Anzeiger, 172, pp. 78-79, (1991)
[108]  
Singcr S.A., Robinson M.O., Bellv A.R., Simon M.I., Riggs A.D., Measurement by quantitative PCR of changes in HPRT. PGK-I, PGK-2, APRT, MTase, and Zfy gene transcripts during mouse spermatogenesis. Nucleic Acids Res, 18. 1255, (1990)
[109]  
Singh L., Jones K.W., Sex reversal in the mouse (Mus musculum) is caused by a recurrent nonrcciprocal crossover involving the X and an aberrant Y chromosome, Cell, 28, pp. 205-216, (1982)
[110]  
Snow M., Autonomous development of parts isolated from pnmitivc-streak-stagc mouse embryos. Is development clonal, J. Embryol. Exp. Morphol, 65, 1, pp. 269-287, (1981)