Ai J.W., Zhu Y., Duan J., Yu Q.Y., Zhang G.J., Wan F. and Xiang Z.H. (2011) Genome-wide
analysis of cytochrome P450 monooxygenase genes in the silkworm, Bombyx mori. Gene,
480, 42-50.
Ashok M., Turner C. and Wilson T.G. (1998) Insect juvenile hormone resistance gene
homology with the bHLH-PAS family of transcriptional regulators. Proceedings of the
National Academy of Sciences of the United States of America, 95, 2761-2766.
Carninci P., Westover A., Nishiyama Y., Ohsumi T., Itoh M., Nagaoka S., Sasaki N.,
Okazaki Y., Muramatsu M., Schneider C. and Hayashizaki Y. (1997) High efficiency
selection of full-length cDNA by improved biotinylated cap trapper. DNA Research, 4, 6166.
Charles J.P., Iwema T., Epa V.C., Takaki K., Rynes J. and Jindra M. (2011) Ligand-binding
properties of a juvenile hormone receptor, Methoprene-tolerant. Proceedings of the
National Academy of Sciences of the United States of America, 108, 21128-21133.
Delanoue R., Slaidina M. and Leopold P. (2010) The steroid hormone ecdysone controls
systemic growth by repressing dMyc function in Drosophila fat cells. Developmental Cell,
18, 1012-2021.
Denlinger D.L. (2002) Regulation of diapause. Annual Review of Entomology, 47, 93-122.
Denlinger D.L. and Armbruster P.A. (2014) Mosquito diapause. Annual Review of
Entomology, 59, 73-93.
Denlinger D.L., Valaitis A.P. and Lee K.Y. (1997) Further evidence that diapause in the
gypsy moth, Lymantria dispar, is regulated by ecdysteroids: a comparison of diapause and
nondiapause strains. Journal of Insect Physiology, 43, 897-903.
80
Denlinger D.L., Yocum G.D. and Rinehart J.P. (2012) Hormonal control of diapause. Insect
Endocrinology (ed. L.I. Gilbert), 430-463. Academic Press, London.
Egi Y., Akitomo S., Fujii T., Banno Y. and Sakamoto K. (2014) Silkworm strains that can be
clearly destined towards either embryonic diapause or direct development by adjusting a
single ambient parameter during the preceding generation. Entomological Science, 17,
396-399.
Forrest A.R.R., Kawaji H., Rehli M., Baillie J.K., de Hoon M.J.L., Harberle V. et al. (2014)
A promoter-level mammalian expression atlas. Nature, 507, 462-470.
Fukuda S. (1951) The production of the diapause eggs by transplanting the suboesophageal
ganglion in the silkworm. Proceedings of the Japan Academy, 27, 672-677.
Fukuda S. (1952) Function of the pupal brain and suboesophageal ganglion in the production
of non-diapause eggs in the silkworm. Annotationes Zoologicae Japonenses, 25, 149-155.
Gharib B., Legay J.M. and De Reggi M. (1981) Potentiation of developmental abilities of
diapausing eggs of Bombyx mori by 20-hydroxyecdysone. Journal of Insect Physiology,
27, 711-713.
Guittard E., Blais C., Maria A., Parvy J.P., Pasricha S., Lumb C., Lafont R., Daborn P.J. and
Dauphin-Villenmant C. (2011) CYP18A1, a key enzyme of Drosophila steroid hormone
inactivation, is essential for metamorphosis. Developmental Biology, 349, 35-45.
Haberle V., Forrest A.R.R., Hayashizaki Y., Carninci P. and Lenhard B. (2015) CAGEr:
precise TSS data retrieval and high-resolution promoterome mining for integrative
analyses. Nucleic Acids Research, 43, e51.
Hasegawa K. and Shimizu I. (1987) In vivo and in vitro photoperiodic induction of diapause
using isolated brain-suboesophageal ganglion complexes of the silkworm, Bombyx mori.
Journal of Insect Physiology, 33, 959-966.
81
Hou Z., Gangjee A. and Matherly L.H. (2022) The evolving biology of the proton-coupled
folate transporter: New insights into regulation, structure, and mechanism. The FASEB
Journal, 36, e22164.
Ikeda K., Daimon T., Sezutsu H., Udaka H. and Numata H. (2019) Involvement of the Clock
Gene period in the Circadian Rhythm of the Silkmoth Bombyx mori. Journal of Biological
Rhythms, 34, 283-292.
Ikeno T., Tanaka S., Numata H. and Goto S.G. (2010) Photoperiodic diapause under the
control of circadian clock genes in an insect. BMC Biology, 8, 116.
石黒 慎一, 小島 信幸, 鈴木 幸一 (2015) コガタルリハムシの成虫休眠機構. 蚕糸・昆虫
バイオテック, 84, 145-154.
Itoh M., Kojima M., Nagao-Sato S., Saijo E., Lassmann T., Kanamori-Katayama M., Kaiho
A., Lizio M., Kawaji H., Carninci P., Forest R.R.A. and Hayashizaki Y. (2012) Automated
workflow for preparation of cDNA for cap analysis of gene expression on a single
molecule sequencer. PLos One, 7, e30809.
Jiang X.F., Huang S.H. and Luo L.Z. (2011) Juvenile hormone changes associated with
diapause induction, maintenance, and termination in the beet webworm, Loxostege
sticticalis (Lepidoptera: Pyralidae). Archives of Insect Biochemistry and Physiology, 77,
134-144.
Kanamori-Katayama M., Itoh M., Kawaji H., Lassmann T., Katayama S., Kojima M., Bertin
N., Kaiho A., Ninomiya N., Daub C.O., Carninci P., Forest R.R.A. and Hayashizaki Y.
(2011) Unamplified cap analysis of gene expression on a single-molecule sequencer.
Genome Research, 21, 1150-1159.
Kayukawa T., Minakuchi C., Namiki T., Togawa T., Yoshiyama M., Kamimura M., Mita K.,
Imanishi S., Kiuchi M., Ishikawa Y. and Shinoda T. (2012) Transcriptional regulation of
juvenile hormone-mediated induction of Krüppel homolog 1, a repressor of insect
82
metamorphosis. Proceedings of the National Academy of Sciences of the United States of
America, 109, 11729-11734.
Kayukawa T., Murata M., Kobayashi I., Muramatsu D., Okada C., Uchino K., Sezutsu H.,
Kiuchi M., Tamura T., Hiruma K., Ishikawa Y. and Shinoda T. (2014) Hormonal
regulation and developmental role of Krüppel homolog 1, a repressor of metamorphosis, in
the silkworm Bombyx mori. Developmental Biology, 388, 48-56.
Kodzius R., Kojima M., Nishiyori H., Nakamura M., Fukuda S., Tagami M., Sasaki D.,
Imamura K., Kai C., Harbers M., Hayashizaki Y. and Carninci P. (2006) CAGE: cap
analysis of gene expression. Nature Methods, 3, 211-22.
Kogure M. (1933) The influence of light and temperature on certain characters of the
silkworm, Bombyx mori. Journal of the Department of Agriculture, Kyushu Imperial
University, 4, 1-93.
Konopova B., Smykal V. and Jindra M. (2011) Common and distinct roles of juvenile
hormone signaling genes in metamorphosis of holometabolous and hemimetabolous
insects. PLoS ONE, 6, e28728.
Kozlova T. and Thummel C.S. (2003) Essential roles for ecdysone signaling during
Drosophila mid-embryonic development. Science, 301, 1911-1914.
Lee K.Y. and Denlinger D.L. (1997) A role for ecdysteroids in the induction and
maintenance of the pharate first instar diapause of the gypsy moth, Lymantria dispar.
Journal of Insect Physiology, 43, 289-296.
Li H. and Durbin R. (2009) Fast and accurate short read alignment with Burrows-Wheeler
transform. Bioinformatics, 25, 1754-1760.
Li M., Mead E.A. and Zhu J.S. (2011) Heterodimer of two bHLH-PAS proteins mediates
juvenile hormone-induced gene expression. Proceedings of the National Academy of
Sciences of the United States of America, 108, 638-643.
83
Li Z.Q., Ge X., Ling L., Zeng B.S., Xu J., Aslam A.F.M., You L., Palli S.R., Huang Y.P. and
Tan A.J. (2014) CYP18A1 regulates tissue-specific steroid hormone inactivation in
Bombyx mori. Insect Biochemistry and Molecular Biology, 54, 33-41.
Lozano J. and Bells X. (2011) Conserved repressive function of Krüppel homolog 1 on insect
metamorphosis in hemimetabolous and holometabolous species. Scientific Reports, 1, 163.
Makka T., Seino A., Tomita S., Fujiwara H. and Sonobe H. (2002) A possible role of 20hydroxyecdysone in embryonic development of the silkworm Bombyx mori. Archives of
Insect Biochemistry and Physiology, 51, 111-120.
Miki T., Shinohara T., Chafino S., Noji S. and Tomioka K. (2020) Photoperiod and
temperature separately regulate nymphal development through JH and insulin/TOR
signaling pathways in an insect. Proceedings of the National Academy of Sciences, 117,
5525-5531.
Minakuchi C., Namiki T. and Shinoda T. (2009) Krüppel homolog 1, an early juvenile
hormone-response gene downstream of Methoprene-tolerant, mediates its antimetamorphic action in the red flour beetle Tribolium castaneum. Developmental Biology,
325, 341-350.
Minakuchi C., Zhou X. and Riddiford L.M. (2008) Krüppel homolog 1 (Kr-h1) mediates
juvenile hormone action during metamorphosis of Drosophila melanogaster. Mechanisms
of Development, 125, 91-105.
Miura K., Oda M., Makita S. and Chinzei Y. (2005) Characterization of the Drosophila
Methoprene-tolerant gene product. Juvenile hormone binding and ligand-dependent gene
regulation. The FEBS Journal, 272, 1169-1178.
Mori A., Oda T. and Wada Y. (1981) Studies on the Egg Diapause and Overwintering of
Aedes albopictus in Nagasaki. Tropical medicine, 23, 79-90.
84
Moribayashi A., Shudo C. and Kurahashi H. (2001) Latitudinal variation in the incidence of
pupal diapause in Asian and Oceanian populations of the flesh fly, Boettcherisca
peregrina (Diptera: Sarcophagidae). Medical Entomology and Zoology, 52, 263-268.
Morohoshi S. and Ishida S. (1975) The control of growth and development in Bombyx mori.
XXV. Induction of supernumerary larval ecdysis and non-diapause eggs by injection of
the juvenile hormone. Proceedings of the Japan Academy, 51, 62-67.
Morohoshi S., Ishida S. and Fugo H. (1972) The control of growth and development in
Bombyx mori. XVIII. Production of non-diapause eggs by injection of the juvenile
hormone. Proceedings of the Japan Academy, 48, 736-741.
Murata M., Nishiyori-Sueki H., Kojima-Ishiyama M., Carninci P., Hayashizaki Y. and Itoh
M. (2014) Detecting expressed genes using CAGE. Methods in Molecular Biology, 1164,
67-85.
Mukai A., Mano G., Marteaux L.D., Shinada T. and Goto S.G. (2022) Juvenile hormone as a
causal factor for maternal regulation of diapause in a wasp. Insect Biochemistry and
Molecular Biology, 144, 103758.
Nakamura Y., Gotoh T., Imanishi S., Mita K., Kurtti T.J. and Noda H. (2011) Differentially
expressed genes in silkworm cell cultures in response to infection by Wolbachia and
Cardinium endosymbionts. Insect Molecular Biology, 20, 279-289.
Nijhout H.F. (1994) Insect Hormones. Princeton University Press, New Jersey.
Numata H., Shiga S. and Morita A. (1997) Photoperiodic receptors in arthropods. Zoological
Science, 14, 187-197.
Rewitz K.F., Yamanaka N. and O’Connor M.B. (2010) Steroid hormone inactivation is
required during the juvenile-adult transition in Drosophila. Developmental Cell, 19, 895902.
85
Richard D.S., Warrent J.T., Saunders D.S. and Gilbert L.I. (1987) Haemolymph ecdysteroid
titres in diapause- and non-diapause-destined larvae and pupae of Sarcophaga
argyrostoma. Journal of Insect Physiology, 33, 115-122.
Panthee S., Paudel A., Hamamoto H. and Sekimizu K. (2017) Advantages of the Silkworm
As an Animal Model for Developing Novel Antimicrobial Agents. Frontiers in
Microbiology, 8, 373.
Riddiford L.M., Truman J.W., Mirth C.K. and Shen Y.C. (2010) A role for juvenile hormone
in the prepupal development of Drosophila melanogaster. Development, 137, 1117-1126.
Sakamoto T., Uryu O. and Tomioka K. (2011) The clock gene period plays an essential role
in photoperiodic control of nymphal development in the cricket Modicogryllus siamensis.
Journal of Insect Physiology, 57, 538-556.
Saunders D.S. (1966) Larval diapause of maternal origin - II. The effect of photoperiod and
temperature on Nasonia vitripennis. Journal of Insect Physiology, 12, 569-581.
D.S. ソーンダース (1981) 昆虫時計 初版 正木進三訳, 339-349. サイエンス社, 東京.
Shinoda T. and Itoyama K. (2003) Juvenile hormone acid methyltransferase: A key
regulatory enzyme for insect metamorphosis. Proceedings of the National Academy of
Sciences of the United States of America, 100, 11986-11991
Sim C. and Denlinger D.L. (2009) A shut-down in expression of an insulin-like peptide, ILP1, halts ovarian maturation during the overwintering diapause of the mosquito Culex
pipiens. Insect Molecular Biology, 18, 325-332.
Smykal V., Daimon T., Kayukawa T., Takaki K., Shinoda T. and Jindra M. (2014)
Importance of juvenile hormone signaling arises with competence of insect larvae to
metamorphose. Developmental Biology, 390, 221-230.
Suetsugu Y., Futahashi R., Kanamori H., Kadono-Okuda K., Sasanuma S., Narukawa J.,
Ajimura M., Jouraku A., Namiki N., Shimomura M., Sezutsu H., Osanai-Futahashi M.,
86
Suzuki M.G., Daimon T., Shinoda T., Taniai K., Asaoka K., Niwa R., Kawaoka S.,
Katsuma S., Tamura T., Noda H., Kasahara M., Sugano S., Suzuki Y., Fujiwara H.,
Kataoka H., Arunkumar K.P., Tomar A., Nagaraju J., Goldsmith M.R., Feng Q.L., Xia
Q.Y., Yamamoto K., Shimada T. and Mita K. (2013) Large scale full-length cDNA
sequencing reveals a unique genomic landscape in a lepidopteran model insect, Bombyx
mori. G3 (Bethesda), 3, 1481-1492.
Tabunoki H., Ono H., Ode H., Ishikawa K., Kawana N., Banno Y., Shimada T., Nakamura Y.,
Yamamoto K., Satoh J.I. and Bono H. (2013) Identification of key uric acid synthesis
pathway in a unique mutant silkworm Bombyx mori model of Parkinson’s disease. PLoS
ONE, 7, e69130.
Tanaka Y. (1950) Studies on hibernation with special reference to photoperiodicity and
breeding of Chinese tussar-silkworm (Ⅱ). The Journal of Sericultural Science of Japan,
19, 429-446.
Tomioka K. and Sakamoto T. (2007) Effects of unilateral compound-eye removal on the
photoperiodic responses of nymphal development in the cricket Modicogryllus siamensis.
Zoological Science, 24, 604-610.
Tschuch C., Schulz A., Pscherer A., Werft W., Benner A., Hotz-Wagenblatt A. Barrionuevo
L.S., Litcher P. and Metens D. (2008) Off-target effects of siRNA specific for GFP. BMC
Molecular Biology, 9, 60.
Tsuchida K. and Yoshitake N. (1979) Effect of environmental condition on the voltinism of
the silkworm, Bombyx mori reared on artificial diets. The Japanese Society of Sericultural
Science, 48, 469-472.
Wang Q., Mohamed A.A.M. and Takeda M. (2013) Serotonin receptor B may lock the gate
of PTTH release/synthesis in the Chinese Silk Moth, Antheraea pernyi; A diapause
initiation/maintenance mechanism? PLoS One, 8, e79381.
87
Watanabe K. (1924) Studies on the voltinism of the silkworm, Bombyx mori. Bulletin of the
Sericultural Experiment Station, 6, 411-455.
Williams C.M. and Adkisson P.L. (1964) Photoperiodic Control of Pupal Diapause in the
Silkworm, Antheraea pernyi. Science, 144, 569.
Wilson T.G. and Fabian J. (1986) A Drosophila melanogaster mutant resistant to a chemical
analog of juvenile hormone. Developmental Biology, 118, 190-201.
Yagi S. and Fukaya M. (1974) Juvenile Hormone As a Key Factor Regulating Larval
Diapause of the Rice Stem Borer, Chilo suppressalis (Lepidoptera: Pyralidae). Applied
Entomology and Zoology, 9, 247-255.
Yamashita O. and Hasegawa K. (1966) Further studies on the mode of action of the diapause
hormone in the silkworm, Bombyx mori L. Journal of Insect Physiology, 12, 957-962.
You-Jin H., Wen-Xia H. and Bin C. (2014) Comparative analysis of proteins in non- and
summer-diapausing pupae of the onion fly, Delia antiqua (Diptera: Anthomyiidae), using
two-dimensional gel electrophoresis. Acta Entomologica Sinica, 57, 161-167.
Zhang Z.L., Xu J.J., Sheng Z.T., Sui Y.P. and Palli S.R. (2011) Steroid receptor co-activator
is required for juvenile hormone signal transduction through a bHLH-PAS transcription
factor, methoprene tolerant. The Journal of Biological Chemistry, 286, 8437-8447.
Zhao R. and Goldman I.D. (2013) The proton-coupled folate transporter: physiological and
pharmacological roles. Current Opinion in Pharmacology, 13, 875-880.
Zielińska Z.M. and Grzelakowska B. (1965a) Folate derivatives in the metabolism of insects
- I. Mitoses in cells of the follicular epithelium as evoked in Acantholyda nemoralis
Thoms. by folate and its 4-aminoanalogue. Journal of Insect Physiology, 11, 405-411.
Zielińska Z.M. and Grzelakowska B. (1965b) Folate derivatives in the metabolism of insects
– II. Biosynthesis of nucleic acids in the polytrophic ovaries of the diapausing larvae of
88
Acantholyda nemoralis Thoms. as promoted by folic acid and its 4-aminoanalogue.
Journal of Insect Physiology, 11, 431-442.
89
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