| Co-Investigator(Kenkyū-buntansha) |
TANIMURA Teiichi Kyushu University, Grad School Sciences, Assoc Prof, 大学院・理学研究院, 助教授 (20142010)
MATSUMOTO Akira Kyushu University, Res Dev Canter for Higher Education, Assistant, 高等教育センター, 助手 (40229539)
久場 洋之 沖縄県農業試験場, 室長
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| Budget Amount *help |
¥14,800,000 (Direct Cost: ¥14,800,000)
Fiscal Year 2005: ¥1,900,000 (Direct Cost: ¥1,900,000)
Fiscal Year 2004: ¥2,800,000 (Direct Cost: ¥2,800,000)
Fiscal Year 2003: ¥3,100,000 (Direct Cost: ¥3,100,000)
Fiscal Year 2002: ¥7,000,000 (Direct Cost: ¥7,000,000)
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| Research Abstract |
The mechanism by which a clock gene pleiotropically controlling life history and behavioral traits causes reproductive isolation is explained using a model species, the melon fly, Bactrocera cucurbitae (Coquillett) (Diptera : Tephritidae). Melon flies mate once a day, at dusk. The population selected for life history traits exhibits correlated responses in the time of mating during the day. For example, the fly populations selected for faster (slower) development have an earlier (later) time of mating. A circathan rhythm controls the time of mating. The circadian periods in constant darkness were about 22h in lines selected for a short developmental period and about 31 h in lines selected for a long developmental period. The data on crosses between the selected lines indicated that the developmental period is controlled by a polygene, whereas the circadian period may be controlled by a single clock gene. These results suggest a clock gene pleiotropically controls developmental and circ
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adian periods in the melon fly. Reproductive isolation may often evolve as an indirect (pleiotropic) consequence of adaptation to different environments or habitats. For example, niches that are temporally or seasonally offset can select organisms with different developmental characteristics. These development differences can inadvertently cause reproductive isolation by a variety of means including shifts in mating activity patterns. The difference in time of mating between populations selected for developmental period translated into significant prezygotic isolation, as measured by mate choice tests. If the mating time between populations differed more than 1 h, the isolation index was significantly higher than zero. These findings indicate that premating isolation can be established by a pleiotropic effect of a clock gene. There are many examples in which the difference in timing of reproduction prevents gene flow between populations, such as the egg spawning time in marine organisms, the flowering time in angiosperms, and the time of mating in insects. In, such, organisms ; if genetic correlations between circadian rhythm and reproductive traits exist, multifarious divergent selection for life history traits would often accelerate the evolution of reproductive isolation through clock genes. Natural populations may diverge in reproduction time through drift, direct natural selection for time of reproduction, or as a by-product effect of genetic correlations. In any case, clock genes are keys in reproductive isolation. We also analyzed sequence of amino-acid of period and doubletime genes, so called as clock genes, in short and long developmental period lines. The difference in a point amino-acid difference in doubletime was detected between short and long lines, and this difference might be related to the difference in mating time of Bactrocera cucurbitae. To examine this, we need to identify Drosophila melanogaster transjenic system, a null mutant of doubletime. Less
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