Hilscher W
Heinrich Heine University, Duesseldorf, D-40225 Germany.
J Exp Zool. 1999 Oct 15;285(3):197-214.
From the existence of two types of cells for reproduction-the female and male germ cells (GCs)-and by recombination of the genome, evolution proceeded dramatically. Unicellular and multicellular plants frequently are characterized by a sequence of haploid and diploid phases, or generations, with gametes and spores as reproductive cells. Isogamy, anisogamy, and oogamy can be distinguished depending on the GCs that correspond, differ in size, or impose as egg cell and sperm cell. In protozoans, too, species are found in which GCs differ clearly from each other. In the female lineage of angiosperms, a "Keimbahn chain" consisting of five successive germ line cells can be observed. Oogenesis and spermatogenesis are complete in coelenterates and similar in mammals. However, the controlling mechanisms are by far more complex in the latter. This means that the balance of hormonal and vegetative nervous influences (stimulation, inhibition) on gametogenesis is not primarily orientated on the germ line cells themselves, but mostly on the structural and functional situation of the gonads and the individual carriers. This becomes particularly evident in insects, where gametogenesis, on the one side, depends on the development of the rest of the organism but on the other side represents an independent developmental process. The point at which germ line cells and somatic cells separate correlates more or less with the degree of phylogenetic development. In worms, insects, and up to the anurans, a part of the cytoplasm, the so-called germ plasma, is separated for the development of GCs during oogenesis (preformistic development). However, in urodeles, reptiles, birds, and mammals, GCs and somatic cells cannot be distinguished before gastrulation (epigenetic development). In various species (e.g., in some oligochaetes and snails), there exist "double spermatogenic lines." In mammals (probably in other vertebrates and perhaps in various phyla of animals, too), the female Keimbahn is provided with only one proliferation system. The male gametogenesis is equipped with two systems: the first corresponds to the female germ line, the second is responsible for the immense number of gametes produced in the mature testes. In mammals the message to become male lies on the Y-chromosome (on its short arm in man and mouse) and was identified as the gene SRY in human and Sry in mouse. The fertility genes that are responsible for an uninterrupted spermatogenesis, up to fertilizing spermatozoa, are sitting on the long arm of the human Y-chromosome. J. Exp. Zool. (Mol. Dev. Evol.) 285:197-214, 1999.
由于存在两种用于繁殖的细胞——雌性和雄性生殖细胞(GCs),以及基因组的重组,进化进程发生了巨大变化。单细胞和多细胞植物通常以单倍体和二倍体阶段或世代的序列为特征,配子和孢子作为生殖细胞。根据相对应的、大小不同的或作为卵细胞和精子细胞的生殖细胞,可以区分同配生殖、异配生殖和卵配生殖。在原生动物中,也发现了生殖细胞彼此明显不同的物种。在被子植物的雌性谱系中,可以观察到由五个连续生殖细胞组成的“生殖链”。腔肠动物的卵子发生和精子发生是完整的,在哺乳动物中则相似。然而,后者的控制机制要复杂得多。这意味着激素和植物性神经影响(刺激、抑制)对配子发生的平衡,主要不是针对生殖细胞本身,而是主要针对性腺和个体载体的结构和功能状况。这在昆虫中尤为明显,在昆虫中,一方面配子发生取决于生物体其他部分的发育,但另一方面它又是一个独立的发育过程。生殖细胞和体细胞分离的点或多或少与系统发育的程度相关。在蠕虫、昆虫以及直到无尾两栖类动物中,在卵子发生过程中(预成论发育),一部分细胞质,即所谓的生殖质,被分离出来用于生殖细胞的发育。然而,在有尾两栖类动物、爬行动物、鸟类和哺乳动物中,在原肠胚形成之前无法区分生殖细胞和体细胞(后生论发育)。在各种物种中(例如,在一些寡毛纲动物和蜗牛中),存在“双精子发生系”。在哺乳动物中(可能在其他脊椎动物中,也许在各种动物门类中也是如此),雌性生殖链只有一个增殖系统。雄性配子发生有两个系统:第一个与雌性生殖系相对应,第二个负责成熟睾丸中产生的大量配子。在哺乳动物中,决定成为雄性的信息位于Y染色体上(在人类和小鼠中位于其短臂上),在人类中被鉴定为SRY基因,在小鼠中为Sry基因。负责精子发生直至受精精子的生育基因位于人类Y染色体的长臂上。《实验动物学杂志(分子发育与进化)》285:197 - 214,1999年。