Key Laboratory of Horticultural Plant Biology (Ministry of Education), College of Horticulture and Forestry Sciences, Huazhong Agricultural University, Wuhan, 430070, China.
College of Life Science and Technology, Huazhong Agricultural University, Wuhan, 430070, China.
Plant Cell Rep. 2020 Dec;39(12):1609-1622. doi: 10.1007/s00299-020-02587-z. Epub 2020 Sep 8.
The physical locations of citrus centromere are revealed by combining genetic and immunological assays for the first time and nine citrus centromere-specific markers for cytogenetics are mined. Centromere localization is challenging, because highly redundant repetitive sequences in centromeric regions make sequence assembly difficult. Although several citrus genomes have been released, the centromeric regions and their characteristics remain to be elucidated. Here, we mapped citrus centromeres through half-tetrad analysis (HTA) that included the genotyping of 54 tetraploid hybrids derived from 2n megagametophytes of Nadorcott tangor with 212 single nucleotide polymorphism (SNP) markers. The sizes of centromeric regions, which estimated based on the heterozygosity restitution rate pattern along the chromosomes, ranged from 1.12 to 18.19 Mb. We also profiled the binding sequences with the centromere-specific histone variant CenH3 by chromatin immunoprecipitation sequencing (ChIP-seq). Based on the positions of the top ten CenH3-enriched contigs, the sizes of centromeric regions were estimated to range from 0.01 to 7.60 Mb and were either adjacent to or included in the centromeric regions identified by HTA. We used DNA probes from two repeats selected from the centromeric regions and seven CenH3-binding centromeric repeats to verify centromeric locations by fluorescence in situ hybridization (FISH). Centromere localization in citrus will contribute to the mining of centromeric/pericentromeric markers, thus to facilitate the rapid identification of mechanisms underlying 2n gamete formation and serve the polyploidy breeding.
首次结合遗传和免疫测定法揭示了柑橘着丝粒的物理位置,并挖掘了 9 个用于细胞遗传学的柑橘着丝粒特异性标记物。着丝粒定位具有挑战性,因为着丝粒区域中的高度冗余重复序列使得序列组装变得困难。尽管已经发布了几个柑橘基因组,但着丝粒区域及其特征仍有待阐明。在这里,我们通过半四分体分析(HTA)对柑橘着丝粒进行了定位,该分析包括对 212 个单核苷酸多态性(SNP)标记的 54 个四倍体杂种的基因型进行了分析,这些杂种是从 2n 大配子体衍生而来的。根据沿染色体上杂合性恢复率模式估算的着丝粒区域大小范围为 1.12 至 18.19 Mb。我们还通过染色质免疫沉淀测序(ChIP-seq)对与着丝粒特异性组蛋白变体 CenH3 结合的序列进行了分析。根据十个 CenH3 富集的重叠群的位置,着丝粒区域的大小估计范围为 0.01 至 7.60 Mb,要么紧邻 HTA 确定的着丝粒区域,要么包含在其中。我们使用从两个重复序列中选择的两个 DNA 探针和七个 CenH3 结合的着丝粒重复序列通过荧光原位杂交(FISH)验证了着丝粒的位置。柑橘着丝粒的定位将有助于挖掘着丝粒/着丝粒周围标记物,从而促进对 2n 配子形成机制的快速鉴定,并为多倍体育种服务。