دورية أكاديمية
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6Pgdh polymorphism in wild bulb mite populations: prevalence, environmental correlates and life history trade-offs.

التفاصيل البيبلوغرافية
العنوان: 6Pgdh polymorphism in wild bulb mite populations: prevalence, environmental correlates and life history trade-offs.
المؤلفون: Unnikrishnan P; Faculty of Biology, Institute of Environmental Sciences, Jagiellonian University, ul. Gronostajowa 7, 30-387, Kraków, Poland. upranav13@gmail.com., Grzesik S; Faculty of Biology, Institute of Environmental Sciences, Jagiellonian University, ul. Gronostajowa 7, 30-387, Kraków, Poland., Trojańska M; Faculty of Biology, Institute of Environmental Sciences, Jagiellonian University, ul. Gronostajowa 7, 30-387, Kraków, Poland.; Department of Pathobiology, Institute of Microbiology, University of Veterinary Medicine, 1210, Vienna, Austria., Klimek B; Faculty of Biology, Institute of Environmental Sciences, Jagiellonian University, ul. Gronostajowa 7, 30-387, Kraków, Poland., Plesnar-Bielak A; Faculty of Biology, Institute of Environmental Sciences, Jagiellonian University, ul. Gronostajowa 7, 30-387, Kraków, Poland.
المصدر: Experimental & applied acarology [Exp Appl Acarol] 2024 Jun; Vol. 93 (1), pp. 115-132. Date of Electronic Publication: 2024 Apr 10.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: Kluwer Academic Publishers Country of Publication: Netherlands NLM ID: 8507436 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1572-9702 (Electronic) Linking ISSN: 01688162 NLM ISO Abbreviation: Exp Appl Acarol Subsets: MEDLINE
أسماء مطبوعة: Publication: 1999- : Dordrecht : Kluwer Academic Publishers
Original Publication: Amsterdam ; New York : Elsevier, [c1985-
مواضيع طبية MeSH: Phosphogluconate Dehydrogenase*/genetics , Phosphogluconate Dehydrogenase*/metabolism , Polymorphism, Genetic*, Animals ; Male ; Poland ; Acaridae/genetics ; Acaridae/physiology ; Life History Traits ; Female ; Arthropod Proteins/genetics ; Arthropod Proteins/metabolism ; Gene Frequency ; Environment
مستخلص: Genetic polymorphism in key metabolic genes plays a pivotal role in shaping phenotypes and adapting to varying environments. Polymorphism in the metabolic gene 6-phosphogluconate dehydrogenase (6Pgdh) in bulb mites, Rhizoglyphus robini is characterized by two alleles, S and F, that differ by a single amino acid substitution and correlate with male reproductive fitness. The S-bearing males demonstrate a reproductive advantage. Although the S allele rapidly fixes in laboratory settings, the persistence of polymorphic populations in the wild is noteworthy. This study examines the prevalence and stability of 6Pgdh polymorphism in natural populations across Poland, investigating potential environmental influences and seasonal variations. We found widespread 6Pgdh polymorphism in natural populations, with allele frequencies varying across locations and sampling dates but without clear geographical or seasonal clines. This widespread polymorphism and spatio-temporal variability may be attributed to population demography and gene flow between local populations. We found some correlation between soil properties, particularly cation content (Na, K, Ca, and Mg) and 6Pgdh allele frequencies, showcasing the connection between mite physiology and soil characteristics and highlighting the presence of environment-dependent balancing selection. We conducted experimental fitness assays to determine whether the allele providing the advantage in male-male competition has antagonistic effects on life-history traits and if these effects are temperature-dependent. We found that temperature does not differentially influence development time or juvenile survival in different 6Pgdh genotypes. This study reveals the relationship between genetic variation, environmental factors, and reproductive fitness in natural bulb mite populations, shedding light on the dynamic mechanisms governing 6Pgdh polymorphism.
(© 2024. The Author(s).)
References: Begun DJ, Aquadro CF (1994) Evolutionary inferences from DNA variation at the 6-phosphogluconate dehydrogenase locus in natural populations of Drosophila: selection and geographic differentiation. Genetics 136(1):155–171. https://doi.org/10.1093/genetics/136.1.155. (PMID: 10.1093/genetics/136.1.15581381531205767)
Błaś M, Ojrzyńska H (2024) The climate of Poland. In: Migoń P, Jancewicz K (eds) Landscapes and landforms of Poland. Springer International Publishing, Cham, pp 33–51. https://doi.org/10.1007/978-3-031-45762-3_3. (PMID: 10.1007/978-3-031-45762-3_3)
Błażejczyk K (2006) Climate and bioclimate of Poland. In: Degórski M (ed) Natural and human environment of Poland. A geographical review. Polish Academy of Sciences, Stanislaw Leszycki Institute of Geography and Spatial Organization, Polish Geographical Society, Warsaw, pp 31–48.
Brown KE, Kelly JK (2018) Antagonistic pleiotropy can maintain fitness variation in annual plants. J Evol Biol 31(1):46–56. https://doi.org/10.1111/jeb.13192. (PMID: 10.1111/jeb.1319229030895)
Burns JG, Svetec N, Rowe L, Mery F, Dolan MJ, Boyce WT, Sokolowski MB (2012) Gene–environment interplay in Drosophila melanogaster: chronic food deprivation in early life affects adult exploratory and fitness traits. Proc Natl Acad Sci USA 109(supplement_2):17239–17244. https://doi.org/10.1073/pnas.1121265109. (PMID: 10.1073/pnas.1121265109230456443477394)
Chen C, Du P, Zhang Z, Bao D (2023) 6-Phosphogluconate dehydrogenase inhibition arrests growth and induces apoptosis in gastric cancer via AMPK activation and oxidative stress. Open Life Sci 18(1):20220514. https://doi.org/10.1515/biol-2022-0514. (PMID: 10.1515/biol-2022-0514368524009961966)
de Moraes J, Franklin E, de Morais JW, de Souza JLP (2011) Species diversity of edaphic mites (Acari: Oribatida) and effects of topography, soil properties and litter gradients on their qualitative and quantitative composition in 64 km 2 of forest in Amazonia. Exp Appl Acarol 55(1):39–63. https://doi.org/10.1007/s10493-011-9451-7. (PMID: 10.1007/s10493-011-9451-721476120)
Di Bartolomeo F, Malina C, Campbell K, Mormino M, Fuchs J, Vorontsov E, Gustafsson CM, Nielsen J (2020) Absolute yeast mitochondrial proteome quantification reveals trade-off between biosynthesis and energy generation during diauxic shift. Proc Natl Acad Sci USA 117(13):7524–7535. https://doi.org/10.1073/pnas.1918216117. (PMID: 10.1073/pnas.1918216117321843247132131)
Díaz A, Okabe K, Eckenrode CJ, Villani MG, Oconnor BM (2000) Biology, ecology, and management of the bulb mites of the genus Rhizoglyphus (Acari: Acaridae). Exp Appl Acarol 24(2):85–113. https://doi.org/10.1023/A:1006304300657. (PMID: 10.1023/A:100630430065711108390)
Fahrendorf T, Ni W, Shorrosh BS, Dixon RA (1995) Stress responses in alfalfa (Medicago sativa L.) XIX. Transcriptional activation of oxidative pentose phosphate pathway genes at the onset of the isoflavonoid phytoalexin response. Plant Mol Biol 28(5):885–900. https://doi.org/10.1007/BF00042073. (PMID: 10.1007/BF000420737640360)
Ge T, Yang J, Zhou S, Wang Y, Li Y, Tong X (2020) The role of the pentose phosphate pathway in diabetes and cancer. Front Endocrinol 11:365. https://doi.org/10.3389/fendo.2020.00365. (PMID: 10.3389/fendo.2020.00365)
Gerson U, Thorens D (1982) Mating frequency as an indication of food quality for the bulb mite, Rhizoglyphus robini Claparède. Int J Invertebr Reprod 5(4):201–206. https://doi.org/10.1080/01651269.1982.10553470. (PMID: 10.1080/01651269.1982.10553470)
Gerson U, Cohen E, Capua S (1991) Bulb mite, Rhizoglyphus robini (Astigmata: Acaridae) as an experimental animal. Exp Appl Acarol 12(1):103–110. https://doi.org/10.1007/BF01204403. (PMID: 10.1007/BF01204403)
González-Ruiz R, Leyva-Carrillo L, Peregrino-Uriarte AB, Yepiz-Plascencia G (2023) The combination of hypoxia and high temperature affects heat shock, anaerobic metabolism, and pentose phosphate pathway key components responses in the white shrimp (Litopenaeus vannamei). Cell Stress Chaperones 28(5):493–509. https://doi.org/10.1007/s12192-022-01265-1. (PMID: 10.1007/s12192-022-01265-135349096)
Graffelman J, Weir BS (2016) Testing for Hardy-Weinberg equilibrium at biallelic genetic markers on the X chromosome. Heredity 116(6):558–568. https://doi.org/10.1038/hdy.2016.20. (PMID: 10.1038/hdy.2016.20270718444868269)
Hedrick PW (1999) Antagonistic pleiotropy and genetic polymorphism: a perspective. Heredity 82(2):126–133. https://doi.org/10.1038/sj.hdy.6884400. (PMID: 10.1038/sj.hdy.6884400)
Höglund J, Sheldon BC, Hoglund J (1998) The cost of reproduction and sexual selection. Oikos 83(3):478. https://doi.org/10.2307/3546675. (PMID: 10.2307/3546675)
Hollman A, Tchounwou P, Huang H-C (2016) The association between gene-environment interactions and diseases involving the human GST superfamily with SNP variants. Int J Environ Res Public Health 13(4):379. https://doi.org/10.3390/ijerph13040379. (PMID: 10.3390/ijerph13040379270435894847041)
Hou F-Y, Huang J, Yu S-L, Zhang H-S (2007) The 6-phosphogluconate dehydrogenase genes are responsive to abiotic stresses in rice. J Integr Plant Biol 49(5):655–663. https://doi.org/10.1111/j.1744-7909.2007.00460.x. (PMID: 10.1111/j.1744-7909.2007.00460.x)
Hu B, Xie M, Li H, Zhao W, Hu J, Jiang Y, Ji W, Li S, Hong Y, Yang M, Optiz T, Shi Z (2022) Stoichiometry of soil carbon, nitrogen, and phosphorus in farmland soils in southern China: spatial pattern and related dominates. CATENA 217:106468. https://doi.org/10.1016/j.catena.2022.106468. (PMID: 10.1016/j.catena.2022.106468)
Jarzebowska M, Radwan J (2010) Sexual selection counteracts extinction of small populations of the bulb mites. Evolution 64(5):1283–1289. https://doi.org/10.1111/j.1558-5646.2009.00905.x. (PMID: 10.1111/j.1558-5646.2009.00905.x19930452)
Kapahi P, Chen D, Rogers AN, Katewa SD, Li PW-L, Thomas EL, Kockel L (2010) With TOR, less is more: a key role for the conserved nutrient-sensing TOR pathway in aging. Cell Metab 11(6):453–465. https://doi.org/10.1016/j.cmet.2010.05.001. (PMID: 10.1016/j.cmet.2010.05.001205191182885591)
Kauffman FC, Brown JG, Passonneau JV, Lowry OH (1969) Effects of changes in brain metabolism on levels of pentose phosphate pathway intermediates. J Biol Chem 244(13):3647–3653. https://doi.org/10.1016/S0021-9258(18)83418-4. (PMID: 10.1016/S0021-9258(18)83418-45794230)
Kerwin R, Feusier J, Corwin J, Rubin M, Lin C, Muok A, Larson B, Li B, Joseph B, Francisco M, Copeland D, Weinig C, Kliebenstein DJ (2015) Natural genetic variation in Arabidopsis thaliana defense metabolism genes modulates field fitness. eLife 4:e05604. https://doi.org/10.7554/eLife.05604. (PMID: 10.7554/eLife.05604258670144396512)
Kilias G, Alahiotis SN (1985) Indirect thermal selection in Drosophila melanogaster and adaptive consequences. Theor Appl Genet 69–69(5–6):645–650. https://doi.org/10.1007/BF00251117. (PMID: 10.1007/BF00251117)
Konior M, Radwan J, Kołodziejczyk M, Keller L (2006) Strong association between a single gene and fertilization efficiency of males and fecundity of their mates in the bulb mite. Proc R Soc B Biol Sci 273(1584):309–314. https://doi.org/10.1098/rspb.2005.3302. (PMID: 10.1098/rspb.2005.3302)
Koshiba S, Motoike IN, Saigusa D, Inoue J, Aoki Y, Tadaka S, Shirota M, Katsuoka F, Tamiya G, Minegishi N, Fuse N, Kinoshita K, Yamamoto M (2020) Identification of critical genetic variants associated with metabolic phenotypes of the Japanese population. Commun Biol 3(1):662. https://doi.org/10.1038/s42003-020-01383-5. (PMID: 10.1038/s42003-020-01383-5331776157659008)
Kozyra M, Ingelman-Sundberg M, Lauschke VM (2017) Rare genetic variants in cellular transporters, metabolic enzymes, and nuclear receptors can be important determinants of interindividual differences in drug response. Genet Med 19(1):20–29. https://doi.org/10.1038/gim.2016.33. (PMID: 10.1038/gim.2016.3327101133)
Krüger A, Grüning N-M, Wamelink MMC, Kerick M, Kirpy A, Parkhomchuk D, Bluemlein K, Schweiger M-R, Soldatov A, Lehrach H, Jakobs C, Ralser M (2011) The pentose phosphate pathway is a metabolic redox sensor and regulates transcription during the antioxidant response. Antioxid Redox Signal 15(2):311–324. https://doi.org/10.1089/ars.2010.3797. (PMID: 10.1089/ars.2010.379721348809)
Kudureti A, Zhao S, Zhakyp D, Tian C (2023) Responses of soil fauna community under changing environmental conditions. J Arid Land 15(5):620–636. https://doi.org/10.1007/s40333-023-0009-4. (PMID: 10.1007/s40333-023-0009-4)
Landi S, Capasso G, Esposito S (2021) Different G6PDH isoforms show specific roles in acclimation to cold stress at various growth stages of barley (Hordeum vulgare) and Arabidopsis thaliana. Plant Physiol Biochem 169:190–202. https://doi.org/10.1016/j.plaphy.2021.11.017. (PMID: 10.1016/j.plaphy.2021.11.01734801973)
Leigh DM, Smallegange IM (2014) Effects of variation in nutrition on male morph development in the bulb mite Rhizoglyphus robini. Exp Appl Acarol 64(2):159–170. https://doi.org/10.1007/s10493-014-9822-y. (PMID: 10.1007/s10493-014-9822-y24819854)
Li G, Liu P, Zhao J, Su L, Zhao M, Jiang Z, Zhao Y, Yang X (2023) Correlation of microbiomes in “plant-insect-soil” ecosystem. Front Microbiol 14:1088532. https://doi.org/10.3389/fmicb.2023.1088532. (PMID: 10.3389/fmicb.2023.1088532367938809922863)
Łukasiewicz A, Szubert-Kruszyńska A, Radwan J (2017) Kin selection promotes female productivity and cooperation between the sexes. Sci Adv 3(3):e1602262. https://doi.org/10.1126/sciadv.1602262. (PMID: 10.1126/sciadv.1602262283450485351977)
Łukasik P, Zygadło M, Radwan J (2010) The effect of a phosphogluconate dehydrogenase genotype on sperm competitiveness in the bulb mite, Rhizoglyphus robini. In: Sabelis MW, Bruin J (eds) Trends in acarology. Springer Netherlands, Dordrecht, pp 295–297. https://doi.org/10.1007/978-90-481-9837-5_47. (PMID: 10.1007/978-90-481-9837-5_47)
Mérot C, Llaurens V, Normandeau E, Bernatchez L, Wellenreuther M (2020) Balancing selection via life-history trade-offs maintains an inversion polymorphism in a seaweed fly. Nat Commun 11(1):670. https://doi.org/10.1038/s41467-020-14479-7. (PMID: 10.1038/s41467-020-14479-7320153416997199)
Meyer UA, Zanger UM (1997) Molecular mechanisms of genetic polymorphisms of drug metabolism. Annu Rev Pharmacol Toxicol 37(1):269–296. https://doi.org/10.1146/annurev.pharmtox.37.1.269. (PMID: 10.1146/annurev.pharmtox.37.1.2699131254)
Mukherjee D, Saha D, Acharya D, Mukherjee A, Chakraborty S, Ghosh TC (2018) The role of introns in the conservation of the metabolic genes of Arabidopsis thaliana. Genomics 110(5):310–317. https://doi.org/10.1016/j.ygeno.2017.12.003. (PMID: 10.1016/j.ygeno.2017.12.00329247768)
Nielsen UN, Osler GHR, Campbell CD, Burslem DFRP, Van Der Wal R (2010) The influence of vegetation type, soil properties and precipitation on the composition of soil mite and microbial communities at the landscape scale: biogeography of mites and microbes. J Biogeogr 37(7):1317–1328. https://doi.org/10.1111/j.1365-2699.2010.02281.x. (PMID: 10.1111/j.1365-2699.2010.02281.x)
Oakeshott JG, Chambers GK, Gibson JB, Eanes WF, Willcocks DA (1983) Geographic variation in G6pd and Pgd allele frequencies in Drosophila melanogaster. Heredity 50(Pt 1):67–72. https://doi.org/10.1038/hdy.1983.7. (PMID: 10.1038/hdy.1983.76404856)
Oostermeijer JGB, Van Eijck MW, Van Leeuwen NC, Den Nijs JCM (1995) Analysis of the relationship between allozyme heterozygosity and fitness in the rare Gentiana pneumonanthe L. J Evol Biol 8(6):739–759. https://doi.org/10.1046/j.1420-9101.1995.8060739.x. (PMID: 10.1046/j.1420-9101.1995.8060739.x)
Parrett JM, Chmielewski S, Aydogdu E, Łukasiewicz A, Rombauts S, Szubert-Kruszyńska A, Babik W, Konczal M, Radwan J (2022) Genomic evidence that a sexually selected trait captures genome-wide variation and facilitates the purging of genetic load. Nat Ecol Evol 6(9):Article 9. https://doi.org/10.1038/s41559-022-01816-w. (PMID: 10.1038/s41559-022-01816-w)
Pineda A, Kaplan I, Bezemer TM (2017) Steering soil microbiomes to suppress aboveground insect pests. Trends Plant Sci 22(9):770–778. https://doi.org/10.1016/j.tplants.2017.07.002. (PMID: 10.1016/j.tplants.2017.07.00228757147)
Plesnar-Bielak A, Skrzynecka AM, Prokop ZM, Radwan J (2012) Mating system affects population performance and extinction risk under environmental challenge. Proc R Soc B Biol Sci 279(1747):4661–4667. https://doi.org/10.1098/rspb.2012.1867. (PMID: 10.1098/rspb.2012.1867)
Plesnar-Bielak A, Skwierzyńska AM, Radwan J (2020) Sexual and ecological selection on a sexual conflict gene. J Evol Biol 33(10):1433–1439. https://doi.org/10.1111/jeb.13680. (PMID: 10.1111/jeb.1368032654292)
Powers DA, Ropson I, Brown DC, Beneden RV, Cashon R, Gonzalez-Villaseñor LI, DiMichele JA (1986) Genetic variation in Fundulus heteroclitus: geographic distribution. Am Zool 26(1):131–144. (PMID: 10.1093/icb/26.1.131)
Procházka J, Brom J, Št’astný J, Pecharová E (2011) The impact of vegetation cover on temperature and humidity properties in the reclaimed area of a brown coal dump. Int J Min Reclam Environ 25(4):350–366. https://doi.org/10.1080/17480930.2011.623830. (PMID: 10.1080/17480930.2011.623830)
Przesmycka K, Radwan J (2023) Small-scale genetic structure of populations of the bulb mite Rhizoglyphus robini. Exp Appl Acarol 90(3–4):219–226. https://doi.org/10.1007/s10493-023-00807-1. (PMID: 10.1007/s10493-023-00807-13749840010406659)
Radwan J, Siva-jothy MT (1996) The function of post-insemination mate association in the bulb mite, Rhizoglyphus robini. Anim Behav 52(4):651–657. https://doi.org/10.1006/anbe.1996.0209. (PMID: 10.1006/anbe.1996.0209)
Rivera PC, Gardenal CN, Chiaraviglio M (2006) Sex-biased dispersal and high levels of gene flow among local populations in the argentine boa constrictor, Boa constrictor occidentalis. Austral Ecol 31(8):948–955. https://doi.org/10.1111/j.1442-9993.2006.01661.x. (PMID: 10.1111/j.1442-9993.2006.01661.x)
Rix G, Watkins-Dulaney EJ, Almhjell PJ, Boville CE, Arnold FH, Liu CC (2020) Scalable continuous evolution for the generation of diverse enzyme variants encompassing promiscuous activities. Nat Commun 11(1):5644. https://doi.org/10.1038/s41467-020-19539-6. (PMID: 10.1038/s41467-020-19539-6331590677648111)
Robinson MR, Pilkington JG, Clutton-Brock TH, Pemberton JM, Kruuk LEB (2006) Live fast, die young: trade-offs between fitness components and sexually antagonistic selection on weaponry in Soay sheep. Evolution 60(10):2168–2181. https://doi.org/10.1111/j.0014-3820.2006.tb01854.x. (PMID: 10.1111/j.0014-3820.2006.tb01854.x17133873)
Rusuwa BB, Chung H, Allen SL, Frentiu FD, Chenoweth SF (2022) Natural variation at a single gene generates sexual antagonism across fitness components in Drosophila. Curr Biol 32(14):3161-3169.e7. https://doi.org/10.1016/j.cub.2022.05.038. (PMID: 10.1016/j.cub.2022.05.03835700732)
Skwierzyńska AM, Plesnar-Bielak A (2018) Proximate mechanisms of the differences in reproductive success of males bearing different alleles of Pgdh—a gene involved in a sexual conflict in bulb mite. J Evol Biol 31(5):657–664. https://doi.org/10.1111/jeb.13250. (PMID: 10.1111/jeb.1325029469939)
Smallegange IM, Coulson T (2011) The stochastic demography of two coexisting male morphs. Ecology 92(3):755–764. https://doi.org/10.1890/09-2069.1. (PMID: 10.1890/09-2069.121608483)
Stearns SC (1998) The evolution of life histories. Oxford University Press, Oxford. https://doi.org/10.1093/oso/9780198577416.001.0001. (PMID: 10.1093/oso/9780198577416.001.0001)
Stockwell CA, Mulvey M (1998) Phosphogluconate dehydrogenase polymorphism and salinity in the white sands pupfish. Evolution 52(6):1856. https://doi.org/10.2307/2411357. (PMID: 10.2307/241135728565331)
Tambasco-Studart M, Titiz O, Raschle T, Forster G, Amrhein N, Fitzpatrick TB (2005) Vitamin B6 biosynthesis in higher plants. Proc Natl Acad Sci USA 102(38):13687–13692. https://doi.org/10.1073/pnas.0506228102. (PMID: 10.1073/pnas.0506228102161578731224648)
Tilszer M, Antoszczyk K, Ssaek N, Zajaoc E, Radwan J (2006) Evolution under relaxed sexual conflict in the bulb mite Rhizoglyphus robini. Evolution 60(9):1868–1873. https://doi.org/10.1111/j.0014-3820.2006.tb00530.x. (PMID: 10.1111/j.0014-3820.2006.tb00530.x17089971)
Vieille C, Zeikus GJ (2001) Hyperthermophilic enzymes: sources, uses, and molecular mechanisms for thermostability. Microbiol Mol Biol Rev 65(1):1–43. https://doi.org/10.1128/MMBR.65.1.1-43.2001. (PMID: 10.1128/MMBR.65.1.1-43.20011123898499017)
Watts SA, Lawrence JM (1990) The effect of reproductive state, temperature, and salinity on DNA and RNA levels and activities of metabolic enzymes of the Pyloric Ceca in the Sea Star Luidia clathrata (Say). Physiol Zool 63(6):1196–1215. https://doi.org/10.1086/physzool.63.6.30152640. (PMID: 10.1086/physzool.63.6.30152640)
Whitt SR, Wilson LM, Tenaillon MI, Gaut BS, Buckler ES (2002) Genetic diversity and selection in the maize starch pathway. Proc Natl Acad Sci USA 99(20):12959–12962. https://doi.org/10.1073/pnas.202476999. (PMID: 10.1073/pnas.20247699912244216130568)
Zhang Z, Lv Y, Pan H (2013) Cooling and humidifying effect of plant communities in subtropical urban parks. Urban For Urban Green 12(3):323–329. https://doi.org/10.1016/j.ufug.2013.03.010. (PMID: 10.1016/j.ufug.2013.03.010)
Zindel R, Ofek M, Minz D, Palevsky E, Zchori-Fein E, Aebi A (2013) The role of the bacterial community in the nutritional ecology of the bulb mite Rhizoglyphus robini (Acari: Astigmata: Acaridae). FASEB J 27(4):1488–1497. https://doi.org/10.1096/fj.12-216242. (PMID: 10.1096/fj.12-21624223307835)
معلومات مُعتمدة: UMO-2019/33/B/NZ8/02442 Narodowe Centrum Nauki
فهرسة مساهمة: Keywords: Rhizoglyphus robini; 6-Phosphogluconate dehydrogenase; Balancing selection; Genetic polymorphism; Genotype–environment interaction for fitness; Metabolic gene
المشرفين على المادة: EC 1.1.1.43 (Phosphogluconate Dehydrogenase)
0 (Arthropod Proteins)
تواريخ الأحداث: Date Created: 20240410 Date Completed: 20240617 Latest Revision: 20240626
رمز التحديث: 20240626
مُعرف محوري في PubMed: PMC11182828
DOI: 10.1007/s10493-024-00909-4
PMID: 38597987
قاعدة البيانات: MEDLINE
الوصف
تدمد:1572-9702
DOI:10.1007/s10493-024-00909-4