Fruit quality traits play an important role in consumption of kiwiberry(Actinidia arguta).The genetic basis of fruit quality traits in this woody,perennial and dioecious fruit crop remains largely unknown.This study a...Fruit quality traits play an important role in consumption of kiwiberry(Actinidia arguta).The genetic basis of fruit quality traits in this woody,perennial and dioecious fruit crop remains largely unknown.This study aimed to identify the underlying genetic basis of fruit quality traits in A.arguta,using a single nucleotide polymorphism(SNP)genetic linkage map previously developed in a tetraploid F1 population of‘Ruby-3’בKuiLv-M’.The F1 population was phenotyped over three years(2020–2022)for fruit quality traits,including skin color,flesh color,fruit weight,fruit diameter,total soluble solids,fruit longitudinal diameter and fruit shape index.A total of nine QTLs were detected for five traits,explaining 10%–32%of the trait variation.For fruit color,the support interval of a major QTL on LG9 contained an MYB transcription factor MYB110,which was previously demonstrated to control color regulation in kiwifruit,thus suggesting that the MYB110 is the candidate gene for fruit color in kiwiberry.The linked marker for fruit color was validated in an F1 population and 25 kiwiberry cultivars.In conclusion,the knowledge obtained through the QTL mapping is applicable to improve the efficiency and cost-effectiveness in kiwiberry breeding.展开更多
Rose is one of the most important ornamental and economic plants in the world.Modern rose cultivars are primarily tetraploid,and during meiosis,they may exhibit double reduction or preferential chromosome pairing.Ther...Rose is one of the most important ornamental and economic plants in the world.Modern rose cultivars are primarily tetraploid,and during meiosis,they may exhibit double reduction or preferential chromosome pairing.Therefore,the construction of a high density genetic map of tetraploid rose is both challenging and instructive.In this study,a tetraploid rose population was used to conduct a genetic analysis using genome sequencing.A total of 17382 single nucleotide polymorphism(SNP)markers were selected from 2308042 detected SNPs.Combined with 440 previously developed simple sequence repeats(SSR)and amplified fragment length polymorphism(AFLP)markers,a marker dosage of 6885 high quality markers was successfully assigned by GATK software in the tetraploid model.These markers were used in the construction of a high density genetic map,containing the expected seven linkage groups with 6842 markers,a total map length of 1158.9 c M,and an average inter-marker distance of 0.18 c M.Quantitative trait locus(QTL)analysis was subsequently performed to characterize the genetic architecture of petal number and flower diameter.One major QTL(qpnum-3-1)was detected for petal number in three consecutive years,which explained 20.18–22.11%of the variation in petal number.Four QTLs were detected for flower diameter;the main locus,qfdia-2-2,was identified in two consecutive years.Our results will benefit the molecular marker-assisted breeding of modern rose cultivars.In addition,this study provides a guide for the genetic and QTL analysis of autotetraploid plants using sequencing-based genotyping methods.展开更多
The recent completion of the rose genome sequence is not the end of a process,but rather a starting point that opens up a whole set of new and exciting activities.Next to a high-quality genome sequence other genomic t...The recent completion of the rose genome sequence is not the end of a process,but rather a starting point that opens up a whole set of new and exciting activities.Next to a high-quality genome sequence other genomic tools have also become available for rose,including transcriptomics data,a high-density single-nucleotide polymorphism array and software to perform linkage and quantitative trait locus mapping in polyploids.Rose cultivars are highly heterogeneous and diverse.This vast diversity in cultivated roses can be explained through the genetic potential of the genus,introgressions from wild species into commercial tetraploid germplasm and the inimitable efforts of historical breeders.We can now investigate how this diversity can best be exploited and refined in future breeding work,given the rich molecular toolbox now available to the rose breeding community.This paper presents possible lines of research now that rose has entered the genomics era,and attempts to partially answer the question that arises after the completion of any draft genome sequence:‘Now that we have“the”genome,what’s next?’.Having access to a genome sequence will allow both(fundamental)scientific and(applied)breeding-orientated questions to be addressed.We outline possible approaches for a number of these questions.展开更多
基金support from the National Natural Science Foundation of China(Grant No.32001995)the Major Science and Technology Project of Henan Province(Grant No.221100110400)+3 种基金the China Agriculture Research System of MOF and MARA(Grant No.CARS-26)the Special Engineering Science and Technology Innovation,CAAS(Grant No.CAAS-ASTIP-2024-ZFRI).Part of this research was funded under the TKI project:“Novel genetic and genomic tools for polyploid crops”(KV 1605-020BO 26.03009004,BO 50002022)and USDA's National Institute of Food and Agriculture(NIFA)Specialty Crop Research Initiative project“Tools for genomics assisted breeding in polyploids:Development of a community resource”(Grant No.2020-51181-32156/SCRI)received a scholarship from China Scholarship Council(Grant No.202303250034).
文摘Fruit quality traits play an important role in consumption of kiwiberry(Actinidia arguta).The genetic basis of fruit quality traits in this woody,perennial and dioecious fruit crop remains largely unknown.This study aimed to identify the underlying genetic basis of fruit quality traits in A.arguta,using a single nucleotide polymorphism(SNP)genetic linkage map previously developed in a tetraploid F1 population of‘Ruby-3’בKuiLv-M’.The F1 population was phenotyped over three years(2020–2022)for fruit quality traits,including skin color,flesh color,fruit weight,fruit diameter,total soluble solids,fruit longitudinal diameter and fruit shape index.A total of nine QTLs were detected for five traits,explaining 10%–32%of the trait variation.For fruit color,the support interval of a major QTL on LG9 contained an MYB transcription factor MYB110,which was previously demonstrated to control color regulation in kiwifruit,thus suggesting that the MYB110 is the candidate gene for fruit color in kiwiberry.The linked marker for fruit color was validated in an F1 population and 25 kiwiberry cultivars.In conclusion,the knowledge obtained through the QTL mapping is applicable to improve the efficiency and cost-effectiveness in kiwiberry breeding.
基金the National Natural Science Foundation of China(31600565)the Fundamental Research Funds for the Central Public Welfare Research Institutes,China(ZZ13-YQ-053)+1 种基金the Special Fund for Beijing Common Construction Project,ChinaDr.Peter M.Bourke from Plant Breeding,Wageningen University&Research,The Netherlands,was partly funded through the TKI polyploids project(BO-26.03-009-004 and BO-50-002-022)。
文摘Rose is one of the most important ornamental and economic plants in the world.Modern rose cultivars are primarily tetraploid,and during meiosis,they may exhibit double reduction or preferential chromosome pairing.Therefore,the construction of a high density genetic map of tetraploid rose is both challenging and instructive.In this study,a tetraploid rose population was used to conduct a genetic analysis using genome sequencing.A total of 17382 single nucleotide polymorphism(SNP)markers were selected from 2308042 detected SNPs.Combined with 440 previously developed simple sequence repeats(SSR)and amplified fragment length polymorphism(AFLP)markers,a marker dosage of 6885 high quality markers was successfully assigned by GATK software in the tetraploid model.These markers were used in the construction of a high density genetic map,containing the expected seven linkage groups with 6842 markers,a total map length of 1158.9 c M,and an average inter-marker distance of 0.18 c M.Quantitative trait locus(QTL)analysis was subsequently performed to characterize the genetic architecture of petal number and flower diameter.One major QTL(qpnum-3-1)was detected for petal number in three consecutive years,which explained 20.18–22.11%of the variation in petal number.Four QTLs were detected for flower diameter;the main locus,qfdia-2-2,was identified in two consecutive years.Our results will benefit the molecular marker-assisted breeding of modern rose cultivars.In addition,this study provides a guide for the genetic and QTL analysis of autotetraploid plants using sequencing-based genotyping methods.
基金supported in part by the TKI polyploids project‘Novel genetic and genomic tools for polyploid crops’(BO-26.03-009-004 and BO-50-002-022).
文摘The recent completion of the rose genome sequence is not the end of a process,but rather a starting point that opens up a whole set of new and exciting activities.Next to a high-quality genome sequence other genomic tools have also become available for rose,including transcriptomics data,a high-density single-nucleotide polymorphism array and software to perform linkage and quantitative trait locus mapping in polyploids.Rose cultivars are highly heterogeneous and diverse.This vast diversity in cultivated roses can be explained through the genetic potential of the genus,introgressions from wild species into commercial tetraploid germplasm and the inimitable efforts of historical breeders.We can now investigate how this diversity can best be exploited and refined in future breeding work,given the rich molecular toolbox now available to the rose breeding community.This paper presents possible lines of research now that rose has entered the genomics era,and attempts to partially answer the question that arises after the completion of any draft genome sequence:‘Now that we have“the”genome,what’s next?’.Having access to a genome sequence will allow both(fundamental)scientific and(applied)breeding-orientated questions to be addressed.We outline possible approaches for a number of these questions.
