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首页> 外文期刊>BMC Plant Biology >Physical mapping of repetitive oligonucleotides facilitates the establishment of a genome map-based karyotype to identify chromosomal variations in peanut
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Physical mapping of repetitive oligonucleotides facilitates the establishment of a genome map-based karyotype to identify chromosomal variations in peanut

机译:重复寡核苷酸的物理映射有助于建立基于基于地图的核型以鉴定花生的染色体变化

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Chromosomal variants play important roles in crop breeding and genetic research. The development of single-stranded oligonucleotide (oligo) probes simplifies the process of fluorescence in situ hybridization (FISH) and facilitates chromosomal identification in many species. Genome sequencing provides rich resources for the development of oligo probes. However, little progress has been made in peanut due to the lack of efficient chromosomal markers. Until now, the identification of chromosomal variants in peanut has remained a challenge. A total of 114 new oligo probes were developed based on the genome-wide tandem repeats (TRs) identified from the reference sequences of the peanut variety Tifrunner (AABB, 2n?=?4x?=?40) and the diploid species Arachis ipaensis (BB, 2n?=?2x?=?20). These oligo probes were classified into 28 types based on their positions and overlapping signals in chromosomes. For each type, a representative oligo was selected and modified with green fluorescein 6-carboxyfluorescein (FAM) or red fluorescein 6-carboxytetramethylrhodamine (TAMRA). Two cocktails, Multiplex #3 and Multiplex #4, were developed by pooling the fluorophore conjugated probes. Multiplex #3 included FAM-modified oligo TIF-439, oligo TIF-185-1, oligo TIF-134-3 and oligo TIF-165. Multiplex #4 included TAMRA-modified oligo Ipa-1162, oligo Ipa-1137, oligo DP-1 and oligo DP-5. Each cocktail enabled the establishment of a genome map-based karyotype after sequential FISH/genomic in situ hybridization (GISH) and in silico mapping. Furthermore, we identified 14 chromosomal variants of the peanut induced by radiation exposure. A total of 28 representative probes were further chromosomally mapped onto the new karyotype. Among the probes, eight were mapped in the secondary constrictions, intercalary and terminal regions; four were B genome-specific; one was chromosome-specific; and the remaining 15 were extensively mapped in the pericentric regions of the chromosomes. The development of new oligo probes provides an effective set of tools which can be used to distinguish the various chromosomes of the peanut. Physical mapping by FISH reveals the genomic organization of repetitive oligos in peanut chromosomes. A genome map-based karyotype was established and used for the identification of chromosome variations in peanut following comparisons with their reference sequence positions.
机译:染色体变异在作物育种和遗传研究中起重要作用。单链寡核苷酸(oligo)探针的发展简化了原位杂交(鱼类)的荧光过程,并促进许多物种中的染色体鉴定。基因组测序为寡核糖探针的开发提供丰富的资源。然而,由于缺乏有效的染色体标记,花生在花生中取得了很小的进展。到目前为止,鉴定花生染色体变体仍然是挑战。基于从花生品种Tifrunner(AABB,2Nα= 4x =4x≤4x≤X≤40)的参考序列鉴定的基因组串联重复(TRS),共开发了114个新的寡核苷酸探针(TRS)和二倍体物种Arachis iPaensis( Bb,2n?=?2x?=?20)。基于其位置和染色体中的重叠信号,将这些寡聚探针分为28种。对于每种类型,用绿色荧光素6-羧基荧光素(FAM)或红色荧光素6-羧基甲基甲基溴胺(TMA)选择代表性寡核苷酸。通过汇集荧光团共轭探针开发了两种鸡尾酒,多路复用#3和多路复用#4。 Multiplex#3包括FAM-DEDIFIED OLIGO TIF-439,OLIGO TIF-185-1,OLIGO TIF-134-3和OLIGO TIF-165。 Multiplex#4包括TAMRA改装的OLIGO IPA-1162,OLIGO IPA-1137,OLIGO DP-1和OLIGO DP-5。每个鸡尾酒使在原位杂交(GISH)和Silico Mapping中,在顺序鱼/基因组后能够建立基于基于地图的核型。此外,我们确定了通过辐射暴露引起的花生的14个染色体变体。总共28个代表性探针进一步染色到新的核型上。在探针中,八个被映射在次要收缩,插入和终端区域中;四个是b基因组特异性;一个是染色体特异性的;并且剩余的15在染色体的渗透区域中被广泛映射。新的Oligo探针的开发提供了一种有效的工具,可用于区分花生的各种染色体。鱼的物理映射显示了花生染色体中重复寡核苷酸的基因组组织。建立了基于基于地图的核型,并用于鉴定与其参考序列位置的比较后花生的染色体变化。

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