AKITOMO S., EGI Y., NAKAMURA Y., SUETSUGU Y., OISHI K. & SAKAMOTO K. 2017: Genome-wide microarray screening for Bombyx mori genes related to transmitting the determination outcome of whether to produce diapause or nondiapause eggs. — Insect Sci. 24: 187–193.
ARNER E., DAUB C.O., VITTING-SEERUP K., ANDERSSON R., LILJE B., DRABLØS F., LENNARTSSON A., RÖNNERBLAD M., HRYDZIUSZKO O., VITEZIC M. ET AL. 2015: Transcribed enhancers lead waves of coordinated transcription in transitioning mammalian cells. — Science 347: 1010–1014.
CARNINCI P., WESTOVER A., NISHIYAMA Y., OHSUMI T., ITOH M., NAGAOKA S., SASAKI N., OKAZAKI Y., MURAMATSU M., SCHNEIDER C. ET AL. 1997: High efficiency selection of full-length cDNA by improved biotinylated cap trapper. — DNA Res. 4: 61–66.
CARNINCI P., KASUKAWA T., KATAYAMA S., GOUGH J., FRITH M.C., MAEDA N., OYAMA R., RAVASI T., LENHARD B., WELLS C. ET AL. 2005: The transcriptional landscape of the mammalian ge- nome. — Science 309: 1559–1563.
DAIMON T., KOZAKI T., NIWA R., KOBAYASHI I., FURUTA K., NAMIKI T., UCHINO K., BANNO Y., KATSUMA S., TAMURA T. ET AL. 2012: Precocious metamorphosis in the juvenile hormone-deficient mutant of the silkworm, Bombyx mori. — PLoS Genet. 8: e1002486, 13 pp.
DENLINGER D.L. 2022: Insect Diapause. Cambridge University Press, Cambridge, UK, 464 pp.
DENLINGER D.L. & ARMBRUSTER P.A. 2014: Mosquito diapause. — Annu. Rev. Entomol. 59: 73–93.
DENLINGER D.L., YOCUM G.D. & RINCHART J.P. 2012: Hormonal control of diapause. In Gilbert L.I. (eds): Insect Endocrinology. Academic Press, London, pp. 430–463.
EGI Y., AKITOMO S., FUJII T., BANNO Y. & SAKAMOTO K. 2014: Silk-worm strains that can be clearly destined towards either em- bryonic diapause or direct development by adjusting a single ambient parameter during the preceding generation. — Ento- mol. Sci. 17: 396–399.
FORREST A.R.R., KAWAJI H., REHLI M., BAILLIE J.K., DE HOON M.J.L., HARBERLE V., LASSMANN T., KULAKOVSKIY I.V., LIZIO M., ITOH M. ET AL. 2014: A promoter-level mammalian expression atlas. — Nature 507: 462–470.
FUKUDA S. 1951: The production of the diapause eggs by trans- planting the suboesophageal ganglion in the silkworm. — Proc. Jap. Acad. 27: 672–677.
FUKUDA S. 1952: Function of the pupal brain and suboesophageal ganglion in the production of non-diapause eggs in the silk- worm. — Annot. Zool. Jpn. 25: 149–155.
HABERLE V., FORREST A.R.R., HAYASHIZAKI Y., CARNINCI P. & LEN-HARD B. 2015: CAGEr: precise TSS data retrieval and high-res- olution promoterome mining for integrative analyses. — Nucl. Acids Res. 43(8): e51, 11 pp.
HASEGAWA K. 1951: Studies on the voltinism in the silkworm, Bombyx mori L., with special reference to the organs concern- ing determination of voltinism (a preliminary note). — Proc. Jap. Acad. 27: 667–671.
HASEGAWA K. & SHIMIZU I. 1987: In vivo and in vitro photoperi- odic induction of diapause using isolated brain-suboesophageal ganglion complexes of the silkworm, Bombyx mori. — J. In- sect Physiol. 33: 959–966.
HOU Z., GANGJEE A. & MATHERLY L.H. 2022: The evolving biol- ogy of the proton-coupled folate transporter: New insights into regulation, structure, and mechanism. — FASEB J. 36: e22164, 15 pp.
ITOH M., KOJIMA M., NAGAO-SATO S., SAIJO E., LASSMANN T., KANAMORI-KATAYAMA M., KAIHO A., LIZIO M., KAWAJI H., CARNINCI P. ET AL. 2012: Automated workflow for preparation of cDNA for cap analysis of gene expression on a single molecule se- quencer — PLoS ONE 7(1): e30809, 8 pp.
KANAMORI-KATAYAMA M., ITOH M., KAWAJI H., LASSMANN T., KATAYAMA S., KOJIMA M., BERTIN N., KAIHO A., NINOMIYA N., DAUB C.O. ET AL. 2011: Unamplified cap analysis of gene ex- pression on a single-molecule sequencer. — Genome Res. 21: 1150–1159.
KATAYAMA S., TOMARU Y., KASUKAWA K., WAKI K., NAKANISHI M., NAKAMURA M., NISHIDA H., YAP C.C., SUZUKI M., KAWAI J. ET AL. 2005: Antisense transcription in the mammalian transcrip- tome. — Science 309: 1564–1566.
KAYUKAWA T., MINAKUCHI C., NAMIKI T., TOGAWA T., YOSHIYAMA M., KAMIMURA M., MITA K., IMANISHI S., KIUCHI M., ISHIKAWA Y. ET AL. 2012: Transcriptional regulation of juvenile hormone- mediated induction of Krüppel homolog 1, a repressor of insect metamorphosis. — Proc. Natl. Acad. Sci. U.S.A. 109: 11729– 11734.
KAYUKAWA T., MURATA M., KOBAYASHI I., MURAMATSU D., OKADA C., UCHINO K., SEZUTSU H., KIUCHI M., TAMURA T., HIRUMA K. ET AL. 2014: Hormonal regulation and developmental role of Krüppel homolog 1, a repressor of metamorphosis, in the silk- worm Bombyx mori. — Dev. Biol. 388: 48–56.
KODZIUS R., KOJIMA M., NISHIYORI H., NAKAMURA M., FUKUDA S., TAGAMI M., SASAKI D., IMAMURA K., KAI C., HARBERS M. ET AL. 2006: CAGE: cap analysis of gene expression. — Nat. Meth- ods 3: 211–222.
KOGURE M. 1933: The influence of light and temperature on certain characters of the silkworm, Bombyx mori. — J. Dep. Agric. Kyushu Imper. Univ. 4: 1–93.
LI H. & DURBIN R. 2009: Fast and accurate short read alignment with Burrows-Wheeler transform. — Bioinformatics 25: 1754– 1760.
LOZANO J. & BELLS X. 2011: Conserved repressive function of Krüppel homolog 1 on insect metamorphosis in hemimetabol- ous and holometabolous species. — Sci. Rep. 1: 163, 7 pp.
MIKI T., SHINOHARA T., CHAFINO S., NOJI S. & TOMIOKA K. 2022: Photoperiod and temperature separately regulate nymphal de- velopment through JH and insulin/TOR signaling pathways in an insect. — Proc. Natl. Acad. Sci. U.S.A. 117: 5525–5531.
MINAKUCHI C., ZHOU X. & RIDDIFORD L.M. 2008: Krüppel ho-molog 1 (Kr-h1) mediates juvenile hormone action during metamorphosis of Drosophila melanogaster. — Mech. Dev. 125: 91–105.
MINAKUCHI C., NAMIKI T. & SHINODA T. 2009: Krüppel homolog 1, an early juvenile hormone-response gene downstream of Methoprene-tolerant, mediates its anti-metamorphic action in the red flour beetle Tribolium castaneum. — Dev. Biol. 325: 341–350.
MUKAI A., MANO G., MARTEAUX L.D., SHINADA T. & GOTO S.G. 2022: Juvenile hormone as a causal factor for maternal regula- tion of diapause in a wasp. — Insect Biochem. Mol. Biol. 144: 103758, 9 pp.
MURATA M., NISHIYORI-SUEKI H., KOJIMA-ISHIYAMA M., CARNINCI P., HAYASHIZAKI Y. & ITOH M. 2014: Detecting expressed genes using CAGE. — Methods Mol. Biol. 1164: 67–85.
NIJHOUT H.F. 1994: Insect Hormones. Princeton University Press, New Jersey, 280 pp.
SHINODA T. & ITOYAMA K. 2003: Juvenile hormone acid methyl- transferase: A key regulatory enzyme for insect metamorpho- sis. — Proc. Natl. Acad. Sci. U.S.A. 100: 11986–11991.
SMYKAL V., DAIMON T., KAYUKAWA T., TAKAKI K., SHINODA T. & JINDRA M. 2014: Importance of juvenile hormone signaling arises with competence of insect larvae to metamorphose. — Dev. Biol. 390: 221–230.
TAUBER M.J., TAUBER C.A. & MASAKI S. 1986: Seasonal Adapta-tions of Insects. Oxford University Press, Oxford, 416 pp.
TSCHUCH C., SCHULZ A., PSCHERER A., WERFT W., BENNER A., HOTZ- WAGENBLATT A.H., BARRIONUEVO L.S., LICHTER P. & MERTENS D. 2008: Off-target effects of siRNA specific for GFP. — BMC Mol. Biol. 9: 60, 14 pp.
WATANABE K. 1924: Studies on the voltinism of the silkworm, Bombyx mori. — Bull. Sericult. Exp. Stat. 6: 411–455 [in Japa- nese].
YAGI S. & FUKAYA M. 1974: Juvenile hormone as a key factor regulating larval diapause of the rice stem borer, Chilo sup- pressalis (Lepidoptera: Pyralidae). — Appl. Entomol. Zool. 9: 247–255.
YAMASHITA O. & HASEGAWA K. 1966: Further studies on the mode of action of the diapause hormone in the silkworm, Bombyx mori L. — J. Insect Physiol. 12: 957–962.
YOU-JIN H., WEN-XIA H. & 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 Entomol. Sin. 57: 161–167.
ZHAO R. & GOLDMAN I.D. 2013: The proton-coupled folate trans- porter: physiological and pharmacological roles. — Curr. Opin. Pharmacol. 13: 875–880.
ZIELIŃSKA Z.M. & GRZELAKOWSKA B. 1965a: Folate derivatives in the metabolism of insects – I. Mitoses in cells of the fol- licular epithelium as evoked in Acantholyda nemoralis Thoms. by folate and its 4-aminoanalogue. — J. Insect Physiol. 11: 405–411.
ZIELIŃSKA Z.M. & GRZELAKOWSKA B. 1965b: Folate derivatives in the metabolism of insects – II. Biosynthesis of nucleic acids in the polytrophic ovaries of the diapausing larvae of Acantholyda nemoralis Thoms. as promoted by folic acid and its 4-amino- analogue. — J. Insect Physiol. 11: 431–442.