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SWI1 Is Required for Meiotic Chromosome Remodeling Events

机译:SWI1是减数分裂染色体重塑事件所必需的

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The Arabidopsis dsy10 mutant was previously identified as being defective in the synapsis of meiotic chromosomes resulting in male and female sterility.We report:here the molecular analysis of the mutation and show that it represents a T-DNA insertion in the third exon of the SWI1 gene.Four mutations have now been identified in SWI1, several of which exhibit different phenotypes.For example.the swi1-1 and dyad mutations only affect meiosis in megasporocytes,while the swi1-2 and dsy10 mutations block both male and female meiosis.Furthermore,as part of a detailed cytological characterization of dsy10 meiocytes,we identified several differences during male meiosis between the swi1-2 and dys10 mutants, including variations in the formation of axial elements,the distribution of cohesin proteins and the timing of the premature loss of sister chromatid cohesion.We demonstrate that dsy10 represents a complete loss-of-function mutation,while a truncated form of SWI1 iS expressed during meiosis in swi1-2 plants.We further show that dys10 meiocytes exhibit alterations in modified histone patterns.including acetylated histone H3 and dimethylated histone H3-Lysine 4.
机译:拟南芥dsy10突变体先前被鉴定为减数分裂染色体突触中的缺陷,导致雄性和雌性不育。我们在此报道了该突变体的分子分析,并表明它代表了SWI1第三外显子中的T-DNA插入。现已在SWI1中鉴定出四个突变,其中一些表现出不同的表型。例如swi1-1和dyad突变仅影响巨孢细胞的减数分裂,而swi1-2和dsy10突变可阻断男性和女性的减数分裂。作为dsy10减数分裂细胞详细细胞学特征的一部分,我们确定了swi1-2和dys10突变体在雄性减数分裂过程中的几种差异,包括轴向元件形成的变化,黏附素蛋白的分布和早熟的时间。我们证明了dsy10代表一个完整的功能丧失突变,而在减数分裂过程中以截短形式表达了SWI1 iS。在swi1-2植物中,我们进一步表明dys10减数分裂细胞在修饰的组蛋白模式上表现出变化,包括乙酰化的组蛋白H3和二甲基化的组蛋白H3-赖氨酸4。

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