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Synthesis of a Wheat/Maize Hybrid CENH3 Gene, the Genetic Transformation of Wheat, Its Chromosomal Localization and Effects on Chromosome Behaviors in Wheat/Maize Somatic Hybrids

机译:小麦/玉米杂种CENH3基因的合成,小麦的遗传转化,其染色体定位及对小麦/玉米体细胞杂种的染色体行为的影响

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Centromere-specific histone H3 (CENH3) replaces the canonical histone H3 in nucleosomes of functional centromeres, and plays important roles in faithful chromosome segregation during cell division. CENH3 is also important in the recognition of alien centromeres and determines the accommodation or elimination of alien chromosomes in interspecific or intergenic hybridization. In this study, a maize full length CENH3 with a yellow fluorescent protein ( YFP ) tag at C-terminus ( Zm CENH3- YFP ) and a synthetic hybrid wmCENH3 with the N-terminus from wheat CENH3 and the histone fold domain (HFD) from maize tagged with a red fluorescent protein ( RFP ) at the C-terminus (wmCENH3- RFP ) were transformed to wheat by biolistics transformation. Transgenic wheat plants with both Zm CNEH3- YFP and wmCENH3- RFP genes were identified by PCR. The expression of ZmCENH3-YFP was not observed, while the expression of wmCENH3-RFP could be detected by RT-PCR, direct fluorescence microscopy, and immunostaining with anti-RFP antibody. The expressed wmCENH3-RFP was localized to nuclei as dotted patterns, indicating its targeting to wheat centromeres. Somatic hybridization was performed between wmCENH3- RFP transgenic wheat and transgenic maize that expressed a Zm CENH3- YFP gene to investigate chromosome behaviors in somatic hybrids. Cytological and FISH analyses of somatic hybrid cells showed the formation of micronuclei and lagging chromatin in both somatic hybridizations with or without the wmCENH3- RFP transgene, indicating that ectopically expressed wmCENH3 could not overcome chromosome elimination in wheat/maize somatic hybrids. Immunostaining of wmCENH3-RFP and ZmCENH3-YFP in early stage somatic hybrid cells indicated that both wmCENH3-RFP and ZmCENH3-YFP proteins were expressed, but their binding patterns changed from the commonly observed dotted patterns to diffused ones, suggesting that the inactivation of CENH3 might be a factor for chromosome elimination in wheat/maize somatic hybridization.
机译:着丝粒特异性组蛋白H3(CENH3)替代功能着丝粒核小体中的规范组蛋白H3,并在细胞分裂过程中忠实的染色体分离中发挥重要作用。 CENH3在识别外来着丝粒中也很重要,并决定了异种染色体在种间杂交或基因间杂交中的适应或消除。在这项研究中,玉米全长CENH3在C端带有一个黄色荧光蛋白(YFP)标签(Zm CENH3- YFP),而一个合成杂种wmCENH3与N端分别来自小麦CENH3和组蛋白折叠域(HFD)。通过生物弹弹转换将在C端标记有红色荧光蛋白(RFP)的玉米(wmCENH3- RFP)转化为小麦。通过PCR鉴定了具有Zm CNEH3-YFP和wmCENH3-RFP基因的转基因小麦植物。没有观察到ZmCENH3-YFP的表达,而wmCENH3-RFP的表达可以通过RT-PCR,直接荧光显微镜和抗RFP抗体的免疫染色来检测。表达的wmCENH3-RFP以点状图样定位于细胞核,表明其靶向小麦着丝粒。在wmCENH3- RFP转基因小麦和表达Zm CENH3- YFP基因的转基因玉米之间进行了体细胞杂交,以研究体细胞杂种中的染色体行为。体细胞杂种细胞的细胞学和FISH分析表明,无论是否存在wmCENH3- RFP转基因,两种体细胞杂交均形成微核和染色质滞后,表明异位表达的wmCENH3无法克服小麦/玉米体细胞杂种中的染色体消除。 wmCENH3-RFP和ZmCENH3-YFP在早期体细胞杂交中的免疫染色表明wmCENH3-RFP和ZmCENH3-YFP蛋白均表达,但它们的结合模式从通常观察到的点状变为分散型,提示CENH3的失活。可能是小麦/玉米体细胞杂交中消除染色体的一个因素。

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