Richard Cornette

Dr. Richard Cornette

Molecular Biomimetics Research Unit, Institute of Agrobiological Sciences, National Institute of Agriculture and Food Research Organization (NARO), Tsukuba, Japan
orcid

Research Focus & Metrics

Academic Career Length

26Years (2001-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
1 January 2015 in Journal of Clinical Biochemistry and Nutrition
Verified
Journal Article
Open access
PDF file
HIHiroko P. Indo
Hiroko P. Indo
HYHsiu-Chuan Yen
Hsiu-Chuan Yen
INIkuo Nakanishi
Ikuo Nakanishi
KMKen-Ichiro Matsumoto
Ken-Ichiro Matsumoto
MTMasato Tamura
Masato Tamura
Hideyuki MajimaHideyuki Majima
Hideyuki Majima
Japan's largest platform for academic e-journals: J-STAGE is a full text database for reviewed academic papers published by Japanese societies

1 June 2008 in Journal of Insect Physiology
Verified
Journal Article
Closed access
RCRichard Cornette
Richard Cornette
HGHiroki Gotoh
Hiroki Gotoh
SKShigeyuki Koshikawa
Shigeyuki Koshikawa
TMToru Miura
Toru Miura

1 January 2010 in Insect Biochemistry and Molecular Biology
Verified
Journal Article
Closed access
YKYasushi Kanamori
Yasushi Kanamori
ASAyako Saito
Ayako Saito
YHYuka Hagiwara-Komoda
Yuka Hagiwara-Komoda
DTDaisuke Tanaka
Daisuke Tanaka
KMKanako Mitsumasu
Kanako Mitsumasu
TOTakashi Okuda
Takashi Okuda

12 September 2014 in Nature Communications
Verified
Journal Article
Open access
OGOleg Gusev
Oleg Gusev
YSYoshitaka Suetsugu
Yoshitaka Suetsugu
RCRichard Cornette
Richard Cornette
TKTakeshi Kawashima
Takeshi Kawashima
MLMaria D. Logacheva
Maria D. Logacheva
Takahiro KikawadaTakahiro Kikawada
Takahiro Kikawada
Anhydrobiosis represents an extreme example of tolerance adaptation to water loss, where an organism can survive in an ametabolic state until water returns. Here we report the first comparative analysis examining the genomic background of extreme desiccation tolerance, which is exclusively found in larvae of the only anhydrobiotic insect, Polypedilum vanderplanki. We compare the genomes of P. vanderplanki and a congeneric desiccation-sensitive midge P. nubifer. We determine that the genome of the anhydrobiotic species specifically contains clusters of multi-copy genes with products that act as molecular shields. In addition, the genome possesses several groups of genes with high similarity to known protective proteins. However, these genes are located in distinct paralogous clusters in the genome apart from the classical orthologues of the corresponding genes shared by both chironomids and other insects. The transcripts of these clustered paralogues contribute to a large majority of the mRNA pool in the desiccating larvae and most likely define successful anhydrobiosis. Comparison of expression patterns of orthologues between two chironomid species provides evidence for the existence of desiccation-specific gene expression systems in P. vanderplanki.

30 April 2010 in BMC Developmental Biology
Verified
Journal Article
Open access
PDF file
HMHitoshi Miyakawa
Hitoshi Miyakawa
MIMaki Imai
Maki Imai
NSNaoki Sugimoto
Naoki Sugimoto
YIYuki Ishikawa
Yuki Ishikawa
AIAsano Ishikawa
Asano Ishikawa
TMToru Miura
Toru Miura
Background: Numerous cases of predator-induced polyphenisms, in which alternate phenotypes are produced in response to extrinsic stimuli, have been reported in aquatic taxa to date. The genusDaphnia(Branchiopoda, Cladocera) provides a model experimental system for the study of the developmental mechanisms and evolutionary processes associated with predator-induced polyphenisms. InD. pulex, juveniles form neckteeth in response to predatory kairomones released byChaoboruslarvae (Insecta, Diptera).Results: Previous studies suggest that the timing of the sensitivity to kairomones inD. pulexcan generally be divided into the embryonic and postembryonic developmental periods. We therefore examined which of the genes in the embryonic and first-instar juvenile stages exhibit different expression levels in the presence or absence of predator kairomones. Employing a candidate gene approach and identifying differentially-expressed genes revealed that the morphogenetic factors,Hox3,extradenticleandescargot, were up-regulated by kairomones in the postembryonic stage and may potentially be responsible for defense morph formation. In addition, the juvenile hormone pathway genes,JHAMTandMet, and the insulin signaling pathway genes,InRandIRS-1, were up-regulated in the first-instar stage. It is well known that these hormonal pathways are involved in physiological regulation following morphogenesis in many insect species. During the embryonic stage when morphotypes were determined, one of the novel genes identified by differential display was up-regulated, suggesting that this gene may be related to morphotype determination. Biological functions of the up-regulated genes are discussed in the context of defense morph formation.Conclusions: It is suggested that, following the reception of kairomone signals, the identified genes are involved in a series of defensive phenotypic alterations and the production of a defensive phenotype.