FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W2894750263> ?p ?o ?g. }

• W2894750263 endingPage "e0213796" @default.
• W2894750263 startingPage "e0213796" @default.
• W2894750263 abstract "Differences in the timing of exoskeleton melanization and sclerotization are evident when comparing eusocial and solitary bees. This cuticular maturation heterochrony may be associated with life style, considering that eusocial bees remain protected inside the nest for many days after emergence, while the solitary bees immediately start outside activities. To address this issue, we characterized gene expression using large-scale RNA sequencing (RNA-seq), and quantified cuticular hydrocarbon (CHC) through gas chromatography-mass spectrometry in comparative studies of the integument (cuticle plus its underlying epidermis) of two eusocial and a solitary bee species. In addition, we used transmission electron microscopy (TEM) for studying the developing cuticle of these and other three bee species also differing in life style. We found 13,200, 55,209 and 30,161 transcript types in the integument of the eusocial Apis mellifera and Frieseomelitta varia, and the solitary Centris analis, respectively. In general, structural cuticle proteins and chitin-related genes were upregulated in pharate-adults and newly-emerged bees whereas transcripts for odorant binding proteins, cytochrome P450 and antioxidant proteins were overrepresented in foragers. Consistent with our hypothesis, a distance correlation analysis based on the differentially expressed genes suggested delayed cuticle maturation in A. mellifera in comparison to the solitary bee. However, this was not confirmed in the comparison with F. varia. The expression profiles of 27 of 119 genes displaying functional attributes related to cuticle formation/differentiation were positively correlated between A. mellifera and F. varia, and negatively or non-correlated with C. analis, suggesting roles in cuticular maturation heterochrony. However, we also found transcript profiles positively correlated between each one of the eusocial species and C. analis. Gene co-expression networks greatly differed between the bee species, but we identified common gene interactions exclusively between the eusocial species. Except for F. varia, the TEM analysis is consistent with cuticle development timing adapted to the social or solitary life style. In support to our hypothesis, the absolute quantities of n-alkanes and unsaturated CHCs were significantly higher in foragers than in the earlier developmental phases of the eusocial bees, but did not discriminate newly-emerged from foragers in C. analis. By highlighting differences in integument gene expression, cuticle ultrastructure, and CHC profiles between eusocial and solitary bees, our data provided insights into the process of heterochronic cuticle maturation associated to the way of life." @default.
• W2894750263 created "2018-10-12" @default.
• W2894750263 creator A5001372969 @default.
• W2894750263 creator A5005664096 @default.
• W2894750263 creator A5011624590 @default.
• W2894750263 creator A5016370165 @default.
• W2894750263 creator A5020033645 @default.
• W2894750263 creator A5022674796 @default.
• W2894750263 creator A5025662885 @default.
• W2894750263 creator A5028953088 @default.
• W2894750263 creator A5035489445 @default.
• W2894750263 creator A5048832588 @default.
• W2894750263 creator A5050097835 @default.
• W2894750263 creator A5065196233 @default.
• W2894750263 creator A5067459090 @default.
• W2894750263 creator A5076135308 @default.
• W2894750263 creator A5083960045 @default.
• W2894750263 date "2019-03-14" @default.
• W2894750263 modified "2023-10-18" @default.
• W2894750263 title "Exploring integument transcriptomes, cuticle ultrastructure, and cuticular hydrocarbons profiles in eusocial and solitary bee species displaying heterochronic adult cuticle maturation" @default.
• W2894750263 cites W119625346 @default.
• W2894750263 cites W1502842407 @default.
• W2894750263 cites W1509299150 @default.
• W2894750263 cites W1527783404 @default.
• W2894750263 cites W1539107524 @default.
• W2894750263 cites W1589277348 @default.
• W2894750263 cites W1592395964 @default.
• W2894750263 cites W1771596479 @default.
• W2894750263 cites W1855918033 @default.
• W2894750263 cites W1964022496 @default.
• W2894750263 cites W1965848347 @default.
• W2894750263 cites W1970662019 @default.
• W2894750263 cites W1971093032 @default.
• W2894750263 cites W1972924519 @default.
• W2894750263 cites W1973225907 @default.
• W2894750263 cites W1973393227 @default.
• W2894750263 cites W1973512434 @default.
• W2894750263 cites W1977665189 @default.
• W2894750263 cites W1977936945 @default.
• W2894750263 cites W1979713522 @default.
• W2894750263 cites W1981314772 @default.
• W2894750263 cites W1982053542 @default.
• W2894750263 cites W1982274607 @default.
• W2894750263 cites W1984847244 @default.
• W2894750263 cites W1984961515 @default.
• W2894750263 cites W1987081580 @default.
• W2894750263 cites W1987956305 @default.
• W2894750263 cites W1988902941 @default.
• W2894750263 cites W1992365463 @default.
• W2894750263 cites W1993387760 @default.
• W2894750263 cites W1997145651 @default.
• W2894750263 cites W2000032094 @default.
• W2894750263 cites W2000904893 @default.
• W2894750263 cites W2002919985 @default.
• W2894750263 cites W2004373908 @default.
• W2894750263 cites W2006932105 @default.
• W2894750263 cites W2007480067 @default.
• W2894750263 cites W2010081743 @default.
• W2894750263 cites W2011657487 @default.
• W2894750263 cites W2014780134 @default.
• W2894750263 cites W2020244591 @default.
• W2894750263 cites W2021685934 @default.
• W2894750263 cites W2027102545 @default.
• W2894750263 cites W2027182484 @default.
• W2894750263 cites W2027827700 @default.
• W2894750263 cites W2030530458 @default.
• W2894750263 cites W2034975889 @default.
• W2894750263 cites W2035544799 @default.
• W2894750263 cites W2036187255 @default.
• W2894750263 cites W2036897871 @default.
• W2894750263 cites W2038204033 @default.
• W2894750263 cites W2040600570 @default.
• W2894750263 cites W2047747880 @default.
• W2894750263 cites W2049500581 @default.
• W2894750263 cites W2049973401 @default.
• W2894750263 cites W2051148848 @default.
• W2894750263 cites W2051447459 @default.
• W2894750263 cites W2057250255 @default.
• W2894750263 cites W2057886743 @default.
• W2894750263 cites W2058320872 @default.
• W2894750263 cites W2059400043 @default.
• W2894750263 cites W2061323339 @default.
• W2894750263 cites W2061912939 @default.
• W2894750263 cites W2063653861 @default.
• W2894750263 cites W2064033098 @default.
• W2894750263 cites W2065825538 @default.
• W2894750263 cites W2067786443 @default.
• W2894750263 cites W2069791223 @default.
• W2894750263 cites W2072961914 @default.
• W2894750263 cites W2073567437 @default.
• W2894750263 cites W2074024123 @default.
• W2894750263 cites W2074982691 @default.
• W2894750263 cites W2075325547 @default.
• W2894750263 cites W2078813514 @default.
• W2894750263 cites W2085226261 @default.
• W2894750263 cites W2086432032 @default.
• W2894750263 cites W2090666276 @default.
• W2894750263 cites W2094496702 @default.

• next