β染色体片段的分子细胞遗传学定位和着丝点蛋白的免疫染色。

International journal of plant genomics Pub Date : 2009-01-01 Epub Date: 2009-11-08 DOI:10.1155/2009/721091
Daryna Dechyeva, Thomas Schmidt
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引用次数: 4

摘要

通过比较多色FISH,我们对甜菜加成系PRO1和PAT2的小染色体片段进行了物理定位,并分析了重复DNA家族在β属Procumbentes部分种中的分布。使用了6个重复探针,包括基因型特异性探针-卫星pTS4.1、pTS5和pRp34,以及分散重复的pAp4、端粒(TTTAGGG)(n)和保守的18S-5.8S-25S rRNA基因。原生着丝粒组织的Pachytene-FISH分析允许提出PRO1和PAT2片段的起源。通过对野生甜菜和附加品系中重复DNA分布和组织的比较分析,建立了染色体片段的物理模型。免疫染色显示,PRO1染色体片段结合了α -微管蛋白和丝氨酸10-磷酸化的组蛋白H3,这是活性着丝粒所特有的。这是第一次实验检测到β中的着丝点蛋白,表明它们积极参与有丝分裂中的染色体分离。
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Molecular cytogenetic mapping of chromosomal fragments and immunostaining of kinetochore proteins in Beta.

By comparative multicolor FISH, we have physically mapped small chromosome fragments in the sugar beet addition lines PRO1 and PAT2 and analyzed the distribution of repetitive DNA families in species of the section Procumbentes of the genus Beta. Six repetitive probes were applied, including genotype-specific probes-satellites pTS4.1, pTS5, and pRp34 and a dispersed repeat pAp4, the telomere (TTTAGGG)(n), and the conserved 18S-5.8S-25S rRNA genes. Pachytene-FISH analysis of the native centromere organization allowed proposing the origin of PRO1 and PAT2 fragments. Comparative analysis of the repetitive DNA distribution and organization in the wild beet and in the addition lines allowed the development of a physical model of the chromosomal fragments. Immunostaining revealed that the PRO1 chromosome fragment binds alpha-tubulin and the serine 10-phosphorylated histone H3 specific for the active centromere. This is the first experimental detection of the kinetochore proteins in Beta showing their active involvement in chromosome segregation in mitosis.

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