Induction, identification and genetics analysis of tetraploid Actinidia chinensis

Actinidia chinensis is a commercially important fruit, and tetraploid breeding of A. chinensis is of great significance for economic benefit. In order to obtain elite tetraploid cultivars, tetraploid plants were induced by colchicine treatment with leaves of diploid A. chinensis ‘SWFU03’. The result...

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Main Authors: Shengxing Li, Xiaozhen Liu, Huiming Liu, Xianang Zhang, Qinxia Ye, Hanyao Zhang
Format: Article
Language:English
Published: The Royal Society 2019-11-01
Series:Royal Society Open Science
Subjects:
Online Access:https://royalsocietypublishing.org/doi/pdf/10.1098/rsos.191052
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spelling doaj-351df26b57744da1b2588bcbb20b07682020-11-25T04:01:58ZengThe Royal SocietyRoyal Society Open Science2054-57032019-11-0161110.1098/rsos.191052191052Induction, identification and genetics analysis of tetraploid Actinidia chinensisShengxing LiXiaozhen LiuHuiming LiuXianang ZhangQinxia YeHanyao ZhangActinidia chinensis is a commercially important fruit, and tetraploid breeding of A. chinensis is of great significance for economic benefit. In order to obtain elite tetraploid cultivars, tetraploid plants were induced by colchicine treatment with leaves of diploid A. chinensis ‘SWFU03’. The results showed that the best treatment was dipping leaves 30 h in 60 mg l−1 colchicine solutions, with induction rate reaching 26%. Four methods, including external morphology comparison, stomatal guard cell observation, chromosome number observation and flow cytometry analysis were used to identify the tetraploid of A. chinensis. Using the induction system and flow cytometry analysis methods, 187 tetraploid plants were identified. Three randomly selected tetraploid plants and their starting diploid plants were further subjected to transcriptome analysis, real-time quantitative polymerase chain reaction (RT-qPCR) and methylation-sensitive amplification polymorphism (MSAP) analysis. The transcriptome analysis results showed that there were a total of 2230 differentially expressed genes (DEG) between the diploid and tetraploid plants, of which 660 were downregulated and 1570 upregulated. The DEGs were mainly the genes involved in growth and development, stress resistance and antibacterial ability in plants. RT-qPCR results showed that the gene expression levels of the growth and stress resistance of tetraploid plants were higher than those of diploid ones at the transcriptome level. MSAP analysis of DNA methylation results showed that tetraploid plants had lower methylation ratio than diploid ones. The present results were valuable to further explore the epigenetics of diploid and tetraploid kiwifruit plants.https://royalsocietypublishing.org/doi/pdf/10.1098/rsos.191052actinidia chinensiscolchicinetetraploididentificationreal-time quantitative pcrtranscriptome analysis
collection DOAJ
language English
format Article
sources DOAJ
author Shengxing Li
Xiaozhen Liu
Huiming Liu
Xianang Zhang
Qinxia Ye
Hanyao Zhang
spellingShingle Shengxing Li
Xiaozhen Liu
Huiming Liu
Xianang Zhang
Qinxia Ye
Hanyao Zhang
Induction, identification and genetics analysis of tetraploid Actinidia chinensis
Royal Society Open Science
actinidia chinensis
colchicine
tetraploid
identification
real-time quantitative pcr
transcriptome analysis
author_facet Shengxing Li
Xiaozhen Liu
Huiming Liu
Xianang Zhang
Qinxia Ye
Hanyao Zhang
author_sort Shengxing Li
title Induction, identification and genetics analysis of tetraploid Actinidia chinensis
title_short Induction, identification and genetics analysis of tetraploid Actinidia chinensis
title_full Induction, identification and genetics analysis of tetraploid Actinidia chinensis
title_fullStr Induction, identification and genetics analysis of tetraploid Actinidia chinensis
title_full_unstemmed Induction, identification and genetics analysis of tetraploid Actinidia chinensis
title_sort induction, identification and genetics analysis of tetraploid actinidia chinensis
publisher The Royal Society
series Royal Society Open Science
issn 2054-5703
publishDate 2019-11-01
description Actinidia chinensis is a commercially important fruit, and tetraploid breeding of A. chinensis is of great significance for economic benefit. In order to obtain elite tetraploid cultivars, tetraploid plants were induced by colchicine treatment with leaves of diploid A. chinensis ‘SWFU03’. The results showed that the best treatment was dipping leaves 30 h in 60 mg l−1 colchicine solutions, with induction rate reaching 26%. Four methods, including external morphology comparison, stomatal guard cell observation, chromosome number observation and flow cytometry analysis were used to identify the tetraploid of A. chinensis. Using the induction system and flow cytometry analysis methods, 187 tetraploid plants were identified. Three randomly selected tetraploid plants and their starting diploid plants were further subjected to transcriptome analysis, real-time quantitative polymerase chain reaction (RT-qPCR) and methylation-sensitive amplification polymorphism (MSAP) analysis. The transcriptome analysis results showed that there were a total of 2230 differentially expressed genes (DEG) between the diploid and tetraploid plants, of which 660 were downregulated and 1570 upregulated. The DEGs were mainly the genes involved in growth and development, stress resistance and antibacterial ability in plants. RT-qPCR results showed that the gene expression levels of the growth and stress resistance of tetraploid plants were higher than those of diploid ones at the transcriptome level. MSAP analysis of DNA methylation results showed that tetraploid plants had lower methylation ratio than diploid ones. The present results were valuable to further explore the epigenetics of diploid and tetraploid kiwifruit plants.
topic actinidia chinensis
colchicine
tetraploid
identification
real-time quantitative pcr
transcriptome analysis
url https://royalsocietypublishing.org/doi/pdf/10.1098/rsos.191052
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