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By Samols D., Agrawal A., Kushner I.

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Eur J Entomol 105:561–566 Sezutsu H, Tamura T, Yukuhiro K (2008b) Uniform size of leucine-rich repeats in a wild silk moth Saturnia japonica (Lepidoptera Saturniidae) fibroin. Int J Wild Silkmoth Silk 13:53–60 Sezutsu H, Uchino K, Kobayashi I, Tamura T, Yukuhiro K (2010) Extensive sequence rearrangements and length polymorphism in fibroin genes in the wild silkmoth, Antheraea yamamai (Lepidoptera, Saturniidae). Int J Wild Silkmoth Silk 15:35–50 Takei F, Kikuchi Y, Kikuchi A, Mizuno S, Shimura K (1987) Further evidence for importance of the subunit combination of silkfibroin in its efficient secretion from the posterior silk gland cells.

Ambika Publishers, Bombay Kakati LN, Chutia BC (2009) Diversity and ecology of wild sericigenous insects in Nagaland, India. Trop Ecol 50:137–146 Kioko E, Raina S, Mueke JM (1999) Conservation of the African wild silkmoths for economic incentives to rural communities of the Kakamega forest in Kenya. Int J Wild Silkmoth Silk 4:1–5 Kistler P, Spack S (2003) Comparing agricultural systems in two areas of Madagascar. In: Goodman SM, Benstead JP (eds) Natural history of Madagascar. S. L. Craig Kuroda F (2000) Outline of Indonesia wild silkworm development project (practical use of golden cocoon and the world’s biggest moth).

15 Evolution of Fibroins As described above, flc and P25 sequences have presumably evolved in the standard fashion, that is, amino acid sequences changed through point mutations (see Figs. 12). The non-repetitive parts of the fhc sequences have similar tendencies despite of occurrence in the insertion or deletion events (Fig. 10). In contrast, the repetitive region of fhc sequences has evolved in remarkably different manners. g. Antheraea, Pyralidae). 44 K. Yukuhiro et al. g. A. yamamai and A. mylitta) strongly suggest that unequal cross over played a key role in generating structural variations in fibroins.

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