Abstract
PN6024 is an extraordinary mutant strain of the cellular slime mold Polysphondylium pallidum, characterized by having defects in many unlinked genes. New strains with altered development appeared spontaneously as aberrant clones of PN6024. Genetic crosses using the macrocyst sexual cycle were used to show that PN6030 (a clone like PN6024 in phenotype) carries mutations at two loci, emm and hge, whereas PN6031 (a clone of altered morphology) carries in addition a mutation at a third locus, mgt. hge and possibly mgt are linked to the mating type locus mat. The relatively high frequency of recombination between mat and hge is strong evidence that meiosis precedes macrocyst germination. The mutant genes themselves are of interest. A major effect of the emm-1 mutation is to remove the requirement for light to trigger aggregation. hge-1 greatly reduces the frequency of aggregation, whereas mgt-1 greatly increases it under standard conditions. None of these mutations interrupts later development leading to stalks and spore cells. It is hypothesized that all three genes act on steps immediately preceding the differentiation of the founder cells which initiate aggregation.
Full Text
The Full Text of this article is available as a PDF (2.9 MB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- BONNER J. T., HOFFMAN M. E. EVIDENCE FOR A SUBSTANCE RESPONSIBLE FOR THE SPACING PATTERN OF AGGREGATION AND FRUITING IN THE CELLULAR SLIME MOLDS. J Embryol Exp Morphol. 1963 Sep;11:571–589. [PubMed] [Google Scholar]
- Francis D. Acrasin and the development of Polysphondylium pallidum. Dev Biol. 1965 Dec;12(3):329–346. doi: 10.1016/0012-1606(65)90001-1. [DOI] [PubMed] [Google Scholar]
- Francis D., Shaffer A. A mutant strain of Polysphondylium with defects in many genes. Dev Genet. 1988;9(4-5):629–638. doi: 10.1002/dvg.1020090439. [DOI] [PubMed] [Google Scholar]
- Hanna M. H., Cox E. C. The regulation of cellular slime mold development: a factor causing development of Polysphondylium violaceum aggregation-defective mutants. Dev Biol. 1978 Jan;62(1):206–214. doi: 10.1016/0012-1606(78)90102-1. [DOI] [PubMed] [Google Scholar]
- Hanna M. H., Fatone M., Newth-Clark C., Salerno J., Clemans S. Purification, characterization, and partial structure of D factor from Polysphondylium violaceum. Dev Genet. 1988;9(4-5):653–662. doi: 10.1002/dvg.1020090441. [DOI] [PubMed] [Google Scholar]
- Shimomura O., Suthers H. L., Bonner J. T. Chemical identity of the acrasin of the cellular slime mold Polysphondylium violaceum. Proc Natl Acad Sci U S A. 1982 Dec;79(23):7376–7379. doi: 10.1073/pnas.79.23.7376. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Waddell D. R. The spatial pattern of aggregation centres in the cellular slime mould. J Embryol Exp Morphol. 1982 Aug;70:75–98. [PubMed] [Google Scholar]
