scholarly journals EFFECTS OF A JUVENILE HORMONE MIMIC ON MALE AND FEMALE GAMETOGENESIS OF THE MUD-CRAB,RHITHROPANOPEUS HARRISII(GOULD) (BRACHYURA: XANTHIDAE)

1977 ◽  
Vol 152 (2) ◽  
pp. 199-208 ◽  
Author(s):  
GENEVIEVE G. PAYEN ◽  
JOHN D. COSTLOW
1975 ◽  
Vol 26 (2-3) ◽  
pp. 105-111 ◽  
Author(s):  
Kazuo BUEI ◽  
Sumiyo ITO ◽  
Takashi YAMADA ◽  
Shinichi GAMO ◽  
Masaaki KATO

1992 ◽  
Vol 49 (6) ◽  
pp. 1268-1273 ◽  
Author(s):  
Anthony S. Clare ◽  
John D. Costlow ◽  
Hassan M. Bedair ◽  
George Lumb

The regeneration of a cheliped that is autotomised at the final larval stage, the megalopa, of the mud crab Rhithropanopeus harrisii (Gould) forms the basis of an assay for developmental toxicity. Cheliped regeneration is followed through to the third juvenile crab stage; a regenerate that is approximately two thirds full size normally emerges at the moult to the second crab, and full size is attained at crab 3. The absence of a regenerate at crab 2, or a regenerate that is smaller than normal and/or malformed, is scored as abnormal regeneration. Other parameters examined in this assay include survival and duration of development. The assay is of comparatively short duration (approximately 2 wk), and survival is high following autotomy under optimal conditions. Four insecticides and a herbicide have been tested in the assay at lethal and sublethal concentrations. Of these compounds, methomyl, carbofuran, and alachlor induced abnormal regeneration whereas cypermethrin and RH 5849 did not affect regeneration at the concentrations tested. Although reproducibility of results needs improvement, crab limb regeneration is otherwise a practical assay for developmental toxicity.


Genetics ◽  
2002 ◽  
Vol 161 (1) ◽  
pp. 157-170 ◽  
Author(s):  
D Adam Mason ◽  
Robert J Fleming ◽  
David S Goldfarb

Abstract Importin α’s mediate the nuclear transport of many classical nuclear localization signal (cNLS)-containing proteins. Multicellular animals contain multiple importin α genes, most of which fall into three conventional phylogenetic clades, here designated α1, α2, and α3. Using degenerate PCR we cloned Drosophila melanogaster importin α1, α2, and α3 genes, demonstrating that the complete conventional importin α gene family arose prior to the split between invertebrates and vertebrates. We have begun to analyze the genetic interactions among conventional importin α genes by studying their capacity to rescue the male and female sterility of importin α2 null flies. The sterility of α2 null males was rescued to similar extents by importin α1, α2, and α3 transgenes, suggesting that all three conventional importin α’s are capable of performing the important role of importin α2 during spermatogenesis. In contrast, sterility of α2 null females was rescued only by importin α2 transgenes, suggesting that it plays a paralog-specific role in oogenesis. Female infertility was also rescued by a mutant importin α2 transgene lacking a site that is normally phosphorylated in ovaries. These rescue experiments suggest that male and female gametogenesis have distinct requirements for importin α2.


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