2007
DOI: 10.1002/arch.20173
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Identification of Y chromosomal PCR marker and production of a selected strain for molecular sexing in the brown planthopper, Nilaparvata lugens

Abstract: A laboratory colony was established in order to enable molecular sexing in premature stages in the brown planthopper, Nilaparvata lugens. We found four male-specific amplified fragment length polymorphisms (AFLPs) in the planthopper, and sequenced one of the AFLPs along with its 5' flanking region (1,423 bp in total). PCR primers were designed based on the nucleotide sequence information so that the PCR product was present in male planthoppers and absent in female planthoppers. However, we could not completely… Show more

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Cited by 8 publications
(12 citation statements)
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“…The sex difference of genome size may have been due to variation in sex chromosome numbers. Male L. striatellus and S. furcifera have 29 chromosomes whereas female have 30 chromosomes (Kobayashi and Noda, 2007; Noda, 2009). The female hemipterans, L. striatellus, S. furcifera , and C. liydipennis , had larger genomes than the males.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…The sex difference of genome size may have been due to variation in sex chromosome numbers. Male L. striatellus and S. furcifera have 29 chromosomes whereas female have 30 chromosomes (Kobayashi and Noda, 2007; Noda, 2009). The female hemipterans, L. striatellus, S. furcifera , and C. liydipennis , had larger genomes than the males.…”
Section: Resultsmentioning
confidence: 99%
“…These planthoppers are the most destructive rice insect pests in Asia (Noda, 2009; Yin et al, 2014). The chromosome numbers of all 3 are 30 except male S. furcifera and male L. striatellus , which have 29 chromosomes (28+XO) (Kobayashi and Noda, 2007; Noda, 2009). This might explain the fact that male S. furcifera and male L. striatellus have a significantly smaller genome size than females.…”
Section: Discussionmentioning
confidence: 99%
“…As we could not identify the sex of individual nymphs in our mapping populations, we used the Y-specific marker PM3n 63 as a sex-determining locus ( Sex ). In the consensus map, the putative location of PM3n was mapped at the distal end of LG11.…”
Section: Discussionmentioning
confidence: 99%
“…The DNA concentrations were measured and diluted to 50 ng/ml. Primers for a male-specific sequence (PM3nF: 59-GAGCTGGAGTGTGTT GATGT-39 and PM3nR: 59-CAAGTTGATTGAAACAGACT-39) and primers for a sequence common to both sexes (PM3femaleF: 59-ATCATACCCGCATGTTGGAC-39 and 59-GAATCTGAAGGGAGCTGTGC-39) were used, as previously described (Kobayashi and Noda 2007). PCR was performed on 1 ml genomic DNA in a 25-ml reaction mixture (50 units/ml Taq DNA polymerase, W/Mg 2+ buffer for DNA polymerase [Biocolors, Shanghai, China]; 2 mM dNTPs, [TaKaRa]).…”
Section: Pcr Of the Male-specific Genomic Dna Fragmentmentioning
confidence: 99%
“…5C and D). To further confirm the sex of these insects, genomic DNA was isolated for PCR verification, using the male-specific primers PM3n (Kobayashi and Noda, 2007). Because NlFmd is essential for female development, the female embryos likely died without functional NlFmd, resulting in the male-only offspring.…”
Section: Nlfmd Is Required For Female Embryo Developmentmentioning
confidence: 99%