By Scott F. Gilbert
This publication captivates scholar curiosity, establishing minds to the sweetness of developmental biology, when overlaying required fabric with clinical rigour.
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Example text
16). What is the source of this sexual inducer protein? Kirk and Kirk (1986) discovered that the sexual cycle could be initiated by heating dishes of V. carteri to temperatures that might be expected in a shallow pond in late summer. When this was done, the somatic cells of the asexual volvoxes produced the sexual inducer protein. Since the amount of sexual inducer protein secreted by one individual is sufficient to initiate sexual development in over 500 million asexual volvoxes, a single inducing volvox can convert the entire pond to sexuality.
One of the first scientists to test Weismann's hypothesis was Wilhelm Roux, a young German embryologist. In 1888, Roux published the results of a series of defect experiments in which he took 2- and 4-cell frog embryos and destroyed some of the cells of each embryo with a hot needle. Weismann's hypothesis predicted the formation of right or left half-embryos. 14). These developed into halfneurulae having a complete right or left side, with one neural fold, one ear pit, and so on. He therefore concluded that the frog embryo was a mosaic of self-differentiating parts and that it was likely that each cell received a specific set of determinants and differentiated accordingly.
Instead of dividing equally, the chromosomes were hypothesized to divide in such a way that different chromosomal determinants entered different cells. 13). Only in the nuclei of those cells destined to become gametes (the germ cells) were all types of determinants thought to be retained. The nuclei of all other cells would have only a subset of the original determinant types. In postulating this model, Weismann had proposed a hypothesis of development that could be tested immediately. Based on the fate map of the frog embryo, Weismann claimed that when the first cleavage division separated the future right half of the embryo from the future left half, there would be a separation of "right" determinants from "left" determinants in the resulting blastomeres.