English (United Kingdom)

https://curated-unify.zendy.io/wp-json/zendy-region/v1/featured_content/oa?rat=en

https://curated-unify.zendy.io/wp-json/zendy-region/v1/highlighted_journal/

Global: Zendy Plus annual

Presents the access of premium content as premium feature

Premium Content

Presents the keyphrase highlighting as premium feature

Keyphrase Highlighting

Presents the summarisation as premium feature

Summarisation

Insights

Presents the pdf analysis as premium feature

PDF Analysis

Presents the zaia usage as premium feature

ZAIA

Global: Zendy Tools annual

Global: Zendy Free Plan

Global: Zendy Tools monthly

Global: Zendy Plus monthly

Volvox offers a unique opportunity to study the segregation of reproductive potential during development of a multicellular organism. At the sixth cleavage division of an asexual embryo of Volvox carteri, strain HK 10, one half of the 32 cells typically cleave unequally to yield 16 large gonidial (reproductive) initials and 16 smaller somatic initials, while the remaining cells divide equally to generate additional somatic initials (6, 7). Different patterns of unequal cleavage, yielding different numbers and locations of reproductive cells, are observed in sexually induced male and female individuals and in germinating zygotes (6, 7). "Pattern mutants," in which single Mendelian mutations result in modified numbers and/or locations of reproductive cells in asexual or sexual individuals (2, 5), indicate that the process of unequal cleavage is under genetic control; but so far these mutants have not yielded any insight into the mechanism by which the cells undergoing unequal cleavage are specified. Three rather different models that attempt to explain the specification process have been proposed (3, 4, 8). Detailed knowledge of the lineages of cells undergoing unequal division is of obvious significance in attempting to evaluate such models. In a recent paper (1) we reported an extensive scanning EM study of the cleavage patterns and cell lineages in asexual V. carteri (strain HK10) embryos, We showed that because the fourth cleavage is much more oblique than had been reported previously, the four cells constituting each quadrant of a 16cell embryo (cells numbered 1-4 from anterior to posterior pole) overlap much more extensively than had been recognized previously. The result is that after the fifth cleavage, in which each cell divides into an anterior (a) and posterior (p) pair, the anterior hemisphere contains the la, lp, 2a, and 3a cells; not the la, lp, 2a, and 2p cells as previous descriptions of cleavage would have predicted. We then reported, as had Starr earlier (7), that it was the anterior 16 cells that divided unequally to yield gonidial initials. That statement was incorrect. Careful reexamination of side views of embryos before and after the sixth division (Figs. 1 a-c) reveals that the 3a cells of the anterior hemisphere do not divide unequally, but that the 2p cells--although lying in the posterior hemisphere--do. Thus the gonidial initials are derived from the la, lp, 2a, and 2p cells of each quadrant, as Starr (7) originally described, but the gonidia derived from the 2p cells lie in the posterior hemi-

A revision of the cell lineages recently reported for Volvox carteri embryos.