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A method for 3D fluorescence in situ hybridization of poplar root tips based on frozen sections

A technique of fluorescence in situ hybridization and frozen section, which is applied in the field of molecular cytogenetics, can solve the problems of staying, unable to visually display the real space occupancy of chromosomes, and unable to distinguish the real space occupancy of chromosomes in cells, etc.

Active Publication Date: 2021-01-26
NANJING FORESTRY UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, most of the FISH techniques in plants are still at the 2D level, and cannot distinguish the real spatial occupancy of chromosomes in cells.
This is mainly because the production methods of plant FISH are mainly smears, pressed sheets, and drip sheets. Hybrid annealing of sequences, but these production methods change the original spatial position of chromosomes in cells, so they cannot visually display the real spatial occupancy of chromosomes on a three-dimensional level

Method used

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  • A method for 3D fluorescence in situ hybridization of poplar root tips based on frozen sections
  • A method for 3D fluorescence in situ hybridization of poplar root tips based on frozen sections

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Embodiment 1

[0038] 1. Root apex fixation and cleaning

[0039] The young root tips of poplar trees with a length of about 5 mm were intercepted and immediately immersed in Carnot's fixative (3:1 volume ratio of absolute ethanol and glacial acetic acid) for more than 1 h.

[0040] The fixed root tips were washed twice with pure water for 10 min each time to remove Carnot's fixative.

[0041] 2. Embedding, sectioning and washing

[0042] The cleaned root tip was placed on a glass slide, and then the apical tissue with a length of about 2-3 mm was cut off with a double-sided blade, and the excess water on the surface was absorbed with filter paper. The tissue was embedded on the sample head in a cryostat (Leica, CM3050 S) with a special tissue embedding medium (Tissue Freezing Medium, Leica), and the embedded sample was frozen in a cryosection box for 30 min at a temperature of -20 ℃, the temperature of the sample head during sectioning is -16℃, the thickness of the section is 8µm, and the...

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Abstract

The invention discloses a 3D fluorescence in-situ hybridization method for a poplar root tip based on a frozen section, belonging to the field of molecular cytogenetics. The method comprises the following steps: acquiring a poplar root tip, fixing the poplar root tip with a Carnoy's fixative, then performing washing with water, embedding the poplar root tip with an embedding agent, carrying out freezing, conducting slicing, adhering an obtained section onto a glass slide, carrying out FISH steps such as section baking, denaturation, hybridization, antibody detection and the like, and finally carrying out observing under a laser confocal microscope and capturing a 3D image. The method provided by the invention has the advantages that the complete tissue structure of the root tip can be obtained and a FISH signal is clear. Compared with a 2D FISH result obtained by a traditional section preparation method, the method of the invention has the advantages that the method can visually display real space occupation of chromosomes in cells at a three-dimensional level and accurately locate the space distribution of target sequences in the cells at the three-dimensional level, is applicableto the fields of chromosome space occupation and gene expression of poplars, analysis of Hi-C sequencing results and the like, and has wide application prospects.

Description

technical field [0001] The invention belongs to the field of molecular cytogenetics, in particular to a frozen section-based 3D fluorescence in situ hybridization (FISH) method for poplar root tips, which can be used for molecular cytogenetics and epigenetic research of poplar. Background technique [0002] Fluorescence in situ hybridization (FISH) is a molecular cytogenetic technology developed in the 1980s. Based on the principle of base complementary pairing, the DNA or RNA in the sample to be tested is qualitatively, quantitatively or positioned according to the fluorescence signal and then observed under a fluorescence microscope. In the past 20 years, plant FISH technology has made great progress, especially in terms of probe types, from the commonly used rDNA and other repeat-based probes to the current oligonucleotide (Oligo) sequence probes. FISH technology has been widely used in many plant molecular cytogenetics research fields such as karyotype analysis, gene ma...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C12Q1/6841
CPCC12Q1/6841C12Q2527/125C12Q2563/107C12Q2543/10
Inventor 席梦利尚大鑫刘光欣辛昊阳赵乙琏鹿东东宁仪杭
Owner NANJING FORESTRY UNIV
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