Development and application of whole-chromosome painting of chromosomes 7A and 8A of Arachis duranensis based on chromosome-specific single-copy oligonucleotides

Author:

Li Chenyu1ORCID,Fu Liuyang2,Wang Qian23,Liu Hua3,Chen Guoquan23,Qi Feiyan3,Zhang Maoning1,Jia Yaoguang2,Li Xiaona23,Huang Bingyan3,Dong Wenzhao3,Du Pei3ORCID,Zhang Xinyou13ORCID

Affiliation:

1. College of Agriculture, Nanjing Agricultural University, Nanjing, Jiangsu 210095, China

2. College of Life Science, Zhengzhou University, Zhengzhou, Henan 450001, China

3. The Shennong Laboratory/Nation Industrial Innovation Centre for Bio-Breeding/Key Laboratory of Oil Crops in Huang-Huai-Hai Plains, Ministry of Agriculture/Henan Provincial Key Laboratory for Oil Crops Improvement/Institute of Crop Molecular Breeding, Henan Academy of Agricultural Sciences, Zhengzhou, Henan 450002, China

Abstract

For peanut, the lack of stable cytological markers is a barrier to tracking specific chromosomes, elucidating the genetic relationships between genomes and identifying chromosomal variations. Chromosome mapping using single-copy oligonucleotide (oligo) probe libraries has unique advantages for identifying homologous chromosomes and chromosomal rearrangements. In this study, we developed two whole-chromosome single-copy oligo probe libraries, LS-7A and LS-8A, based on the reference genome sequences of chromosomes 7A and 8A of Arachis duranensis. Fluorescence in situ hybridization (FISH) analysis confirmed that the libraries could specifically paint chromosomes 7 and 8. In addition, sequential FISH and electronic localization of LS-7A and LS-8A in A. duranensis (AA) and A. ipaensis (BB) showed that chromosomes 7A and 8A contained translocations and inversions relative to chromosomes 7B and 8B. Analysis of the chromosomes of wild Arachis species using LS-8A confirmed that this library could accurately and effectively identify A genome species. Finally, LS-7A and LS-8A were used to paint the chromosomes of interspecific hybrids and their progenies, which verified the authenticity of the interspecific hybrids and identified a disomic addition line. This study provides a model for developing specific oligo probes to identify the structural variations of other chromosomes in Arachis and demonstrates the practical utility of LS-7A and LS-8A.

Funder

The Major R&D and Promotion Projects in Henan

The National Natural Science Foundation of China

The Fund for Excellent Young Scholars of Henan Academy of Agricultural Sciences

The Key Research Project of the Shennong Laboratory

The Major Science and Technology Projects of Henan Province

The Henan Provincial Agriculture Research System

The China Agriculture Research System

The Key Scientific and Technological Project of Henan Province

Publisher

Canadian Science Publishing

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