FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W2020071611> ?p ?o ?g. }

• W2020071611 abstract "Mapping centromere locations in plant species provides essential information for the analysis of genetic structures and population dynamics. The centromere’s position affects the distribution of crossovers along a chromosome and the parental heterozygosity restitution by 2n gametes is a direct function of the genetic distance to the centromere. Sexual polyploidisation is relatively frequent in Citrus species and is widely used to develop new seedless triploid cultivars. The study’s objectives were to (i) map the positions of the centromeres of the nine Citrus clementina chromosomes; (ii) analyse the crossover interference in unreduced gametes; and (iii) establish the pattern of genetic recombination in haploid clementine gametes along each chromosome and its relationship with the centromere location and distribution of genic sequences. Triploid progenies were derived from unreduced megagametophytes produced by second-division restitution. Centromere positions were mapped genetically for all linkage groups using half-tetrad analysis. Inference of the physical locations of centromeres revealed one acrocentric, four metacentric and four submetacentric chromosomes. Crossover interference was observed in unreduced gametes, with variation seen between chromosome arms. For haploid gametes, a strong decrease in the recombination rate occurred in centromeric and pericentromeric regions, which contained a low density of genic sequences. In chromosomes VIII and IX, these low recombination rates extended beyond the pericentromeric regions. The genomic region corresponding to a genetic distance < 5cM from a centromere represented 47% of the genome and 23% of the genic sequences. The centromere positions of the nine citrus chromosomes were genetically mapped. Their physical locations, inferred from the genetic ones, were consistent with the sequence constitution and recombination pattern along each chromosome. However, regions with low recombination rates extended beyond the pericentromeric regions of some chromosomes into areas richer in genic sequences. The persistence of strong linkage disequilibrium between large numbers of genes promotes the stability of epistatic interactions and multilocus-controlled traits over successive generations but also maintains multi-trait associations. Identification of the centromere positions will allow the development of simple methods to analyse unreduced gamete formation mechanisms in a large range of genotypes and further modelling of genetic inheritance in sexual polyploidisation breeding schemes." @default.
• W2020071611 created "2016-06-24" @default.
• W2020071611 creator A5019686368 @default.
• W2020071611 creator A5033626995 @default.
• W2020071611 creator A5069331475 @default.
• W2020071611 creator A5086193532 @default.
• W2020071611 creator A5086817553 @default.
• W2020071611 creator A5090835901 @default.
• W2020071611 date "2015-03-08" @default.
• W2020071611 modified "2023-10-07" @default.
• W2020071611 title "Genetic mapping of centromeres in the nine Citrus clementina chromosomes using half-tetrad analysis and recombination patterns in unreduced and haploid gametes" @default.
• W2020071611 cites W1535115747 @default.
• W2020071611 cites W1559822611 @default.
• W2020071611 cites W1562687282 @default.
• W2020071611 cites W1599846425 @default.
• W2020071611 cites W1760690168 @default.
• W2020071611 cites W1816371658 @default.
• W2020071611 cites W1909248448 @default.
• W2020071611 cites W1924115295 @default.
• W2020071611 cites W1984328799 @default.
• W2020071611 cites W1985702650 @default.
• W2020071611 cites W1986998800 @default.
• W2020071611 cites W1989035119 @default.
• W2020071611 cites W1993540940 @default.
• W2020071611 cites W1996500038 @default.
• W2020071611 cites W2000408153 @default.
• W2020071611 cites W2005180725 @default.
• W2020071611 cites W2006635798 @default.
• W2020071611 cites W2009223645 @default.
• W2020071611 cites W2015355733 @default.
• W2020071611 cites W2025444328 @default.
• W2020071611 cites W2026535383 @default.
• W2020071611 cites W2029113746 @default.
• W2020071611 cites W2031266176 @default.
• W2020071611 cites W2036988952 @default.
• W2020071611 cites W2042329462 @default.
• W2020071611 cites W2044212895 @default.
• W2020071611 cites W2046707969 @default.
• W2020071611 cites W2052170806 @default.
• W2020071611 cites W2055043387 @default.
• W2020071611 cites W2057393200 @default.
• W2020071611 cites W2057461162 @default.
• W2020071611 cites W2060705689 @default.
• W2020071611 cites W2063275490 @default.
• W2020071611 cites W2067882905 @default.
• W2020071611 cites W2072051455 @default.
• W2020071611 cites W2072213501 @default.
• W2020071611 cites W2074680964 @default.
• W2020071611 cites W2080112545 @default.
• W2020071611 cites W2080815113 @default.
• W2020071611 cites W2084063600 @default.
• W2020071611 cites W2094292633 @default.
• W2020071611 cites W2101780276 @default.
• W2020071611 cites W2105227001 @default.
• W2020071611 cites W2105634166 @default.
• W2020071611 cites W2106096973 @default.
• W2020071611 cites W2111041229 @default.
• W2020071611 cites W2111061681 @default.
• W2020071611 cites W2116477118 @default.
• W2020071611 cites W2119322645 @default.
• W2020071611 cites W2119381112 @default.
• W2020071611 cites W2120741627 @default.
• W2020071611 cites W2125516884 @default.
• W2020071611 cites W2127126022 @default.
• W2020071611 cites W2127490915 @default.
• W2020071611 cites W2128695197 @default.
• W2020071611 cites W2129774153 @default.
• W2020071611 cites W2133218990 @default.
• W2020071611 cites W2136101954 @default.
• W2020071611 cites W2136324352 @default.
• W2020071611 cites W2136897380 @default.
• W2020071611 cites W2138860340 @default.
• W2020071611 cites W2144035729 @default.
• W2020071611 cites W2145430812 @default.
• W2020071611 cites W2150343478 @default.
• W2020071611 cites W2156139952 @default.
• W2020071611 cites W2156259062 @default.
• W2020071611 cites W2163285329 @default.
• W2020071611 cites W2168246640 @default.
• W2020071611 cites W2169678137 @default.
• W2020071611 cites W2171731764 @default.
• W2020071611 cites W2274860283 @default.
• W2020071611 cites W2311474155 @default.
• W2020071611 cites W2586783677 @default.
• W2020071611 cites W2586967340 @default.
• W2020071611 cites W29033112 @default.
• W2020071611 cites W4254248707 @default.
• W2020071611 doi "https://doi.org/10.1186/s12870-015-0464-y" @default.
• W2020071611 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4367916" @default.
• W2020071611 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/25848689" @default.
• W2020071611 hasPublicationYear "2015" @default.
• W2020071611 type Work @default.
• W2020071611 sameAs 2020071611 @default.
• W2020071611 citedByCount "30" @default.
• W2020071611 countsByYear W20200716112015 @default.
• W2020071611 countsByYear W20200716112016 @default.
• W2020071611 countsByYear W20200716112017 @default.
• W2020071611 countsByYear W20200716112018 @default.
• W2020071611 countsByYear W20200716112019 @default.
• W2020071611 countsByYear W20200716112020 @default.

• next