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从单个根尖制备豌豆(Pisum sativum L.)染色体和核悬浮液。

Preparation of pea (Pisum sativum L.) chromosome and nucleus suspensions from single root tips.

机构信息

ENEA, Casaccia Research Centre, Biotechnology and Agriculture Sector, Via Anguillarese 301, I-00100, S.M. di Galeria, Rome, Italy.

出版信息

Theor Appl Genet. 1996 May;92(6):744-51. doi: 10.1007/BF00226097.

Abstract

A high-yield method for the isolation of intact nuclei and chromosomes in suspension from a variable number of pea root tips (1-10) has been developed. This procedure is based on a two-step cell-cycle synchronization of root-tip meristems to obtain a high mitotic index, followed by formaldehyde fixation and mechanical isolation of chromosomes and nuclei by homogenization. In the explant, up to 50% of metaphases were induced through a synchronization of the cell cycle at the G1/S interface with hydroxyurea (1.25 mM), followed, after a 3-h release, by a block in metaphase with amiprophos-methyl (10 μM). The quality and quantity of nuclei and chromosomes were related to the extent of the fixation. Best results were obtained after a 30-min fixation with 2% and 4% formaldehyde for nuclei and chromosomes, respectively. The method described here allowed the isolation of nuclei and chromosomes, even from a single root tip, with a yield of 1×10(5)/root and 1.4×10(5)/root, respectively. Isolated suspensions were suitable for flow cytometric analysis and sorting and PRINS labelling with a rDNA probe.

摘要

已开发出一种从豌豆根尖(1-10)的悬浮液中分离完整核和染色体的高效方法。该方法基于根尖分生组织的两步细胞周期同步化,以获得高有丝分裂指数,然后用甲醛固定,通过匀浆机械分离染色体和核。在外植体中,通过羟基脲(1.25 mM)在 G1/S 界面处同步细胞周期,诱导高达 50%的中期,然后用阿米福酯(10 μM)阻断中期。核和染色体的质量和数量与固定的程度有关。对于核和染色体,分别用 2%和 4%甲醛固定 30 分钟可获得最佳结果。这里描述的方法允许从单个根尖中分离核和染色体,产量分别为 1×10(5)/根和 1.4×10(5)/根。分离的悬浮液适用于流式细胞术分析和分选以及用 rDNA 探针进行 PRINS 标记。

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