RESUMEN
Genetic X environmental interactions are examined at an intrachromosomal level in Drosophila melanogaster. With respect to two fitness components, egg production and egg-to-adult viability, evidence is provided that different segments of the X chromosome are affected differently by each of the chemical substances, zinc sulfate and selenocystine. The extent of a segment's effect on a trait is not always parallelled by the extent of its association with that trait's sensitivity to chemical treatment. Both attributes are functions of the genetical background. The degree of dominance of each segment is not always greater in the chemical environments, a finding inconsistent with Parson's concept of "extreme-environment heterosis".
Asunto(s)
Cistina/análogos & derivados , Drosophila melanogaster/genética , Compuestos de Organoselenio , Selenio/farmacología , Cromosomas Sexuales/efectos de los fármacos , Cromosoma X/efectos de los fármacos , Zinc/farmacología , Animales , Cistina/farmacología , Femenino , Genotipo , Matemática , Oogénesis/efectos de los fármacos , Selección GenéticaRESUMEN
Metabolism of L-[35S]cystathionine, L-[35S]cysteine and L-[35S]homocysteine has been investigated in Astragalus pectinatus. The results indicate that cystathionine undergoes both beta and gamma cleavage to give homocysteine and cysteine. Results also show that cystathionine is synthesized from both cysteine and homocysteine. Furthermore, in addition to the incorporation of 35S into cystathionine, incorporation of 35S from cysteine into methionine and from homocysteine into S-methylcysteine is not only in agreement with the above cystathionine cleavage activities, but also suggests, that transsulfuration in A. pectinatus proceeds in both directions, eg. cysteine leads to cystathionine leads to homocysteine and homocysteine leads to cystathionine leads to cysteine. It is suggested, that the latter reaction may be contributing to the net synthesis of cysteine.