玉米CMS-C同质异核不育系育性恢复的遗传研究
收稿日期: 2017-12-07
修回日期: 2018-02-07
网络出版日期: 2018-04-26
基金资助
国家重点研发计划项目(2016YFD0101206);四川省科技厅支撑计划项目资助(2016NZ0106)
Genetics of fertility restoration in the isocytoplasm allonuclear C-group of cytoplasmic male sterility in maize
Received date: 2017-12-07
Revised date: 2018-02-07
Online published: 2018-04-26
Supported by
Supported by the National Key Research and Development Project of China(2016YFD0101206);the Science and Technology Department of Sichuan Province(2016NZ0106)
玉米是最早利用细胞质雄性不育系生产杂交种的作物之一,C型细胞质雄性不育系(C-type cytoplasmic male sterile, CMS-C)在杂交种生产中具有重要的作用,育性恢复的稳定性直接影响其应用价值。然而,玉米CMS-C的育性恢复机理复杂,且至今仍不明确。为进一步探究玉米CMS-C育性恢复的影响因素,本研究以玉米CMS-C同质异核不育系C48-2、C黄早四和C478为母本,分别与测验系18白、自330、5022以及恢复系A619组配杂交获得F1。其中育性恢复F1通过自交获得F2,并以育性恢复F1为父本分别给育性保持F1授粉,组配双交群体,共获得4个F2群体,6个双交群体。同时以不育系C48-2、C黄早四和C478为母本,各自的保持系48-2、黄早四和478为父本杂交组配不完全双列杂交F1。将所有杂交组合的F1、F2以及双交组合群体分别在不同年份不同地点种植观察,通过植株田间育性调查并结合室内花粉镜检鉴定育性表现。结果表明:1) 同一测验系对玉米CMS-C同质异核不育系的恢保关系不同,暗示不育系的核背景参与调控育性恢复表现;2) 在不同年份不同地点对(C48-2×A619) F2群体进行种植观察,发现不同环境下F2群体可育株与不育株的分离比均符合15∶1,但在云南种植的可育株的育性级别主要为Ⅲ和Ⅳ级,而在四川种植的可育株的育性级别主要为Ⅴ级,表明环境对恢复系A619恢复后代的育性表现有影响;3) 通过恢保关系测定发现18白不能恢复C478,48-2也不能恢复C478,但双交群体[(C478×18白) F1S×(C48-2×18白) F1F]后代却出现了可育株与不育株的分离;同理,双交群体[(C48-2×自330) F1S×(C478×自330) F1F]的后代也出现了可育株与不育株的分离。因此,本文推测C48-2、C478核背景中存在微效恢复基因,这些微效基因与18白、自330中的微效恢复基因通过杂交聚合后能使C478、C48-2的育性恢复,暗示玉米CMS-C的育性恢复呈现一定的剂量效应。这些结果为进一步认识玉米CMS-C育性恢复的复杂性和多样性奠定了基础,为深入研究玉米CMS-C育性恢复机理以及加快CMS-C在不育化制种中的应用提供重要参考。
赵卓凡, 黄玲, 刘永明, 张鹏, 魏桂, 曹墨菊 . 玉米CMS-C同质异核不育系育性恢复的遗传研究[J]. 遗传, 2018 , 40(5) : 402 -414 . DOI: 10.16288/j.yczz.17-401
Maize is one of the first crops to produce hybrids using cytoplasmic male sterile lines. The C-type cytoplasmic male sterile (CMS-C) line is vital for hybrid seed production, and the fertility-restoration reaction along with its stability has a direct bearing on its applications. However, fertility restoration mechanism of CMS-C is complex and is still not clear so far. To further explore the factors affecting the fertility restoration of maize CMS, a series of test crosses were carried out by pollinating the isocytoplasm allonuclear CMS-C lines C48-2, Chuangzaosi and C478 with the test lines 18 bai, zi 330, 5022 and the restorer line A619, respectively. Four F2 populations and six double-cross combinations were obtained from the self-cross of fertility restored F1 and pollinating male-sterility-maintained F1 with the male-fertility-restored F1, respectively. Meanwhile, we developed the incomplete diallel-cross combinations using the isocytoplasm allonuclear male sterile lines as maternal parents and their respective maintainer lines 48-2, huangzaosi and 478 as paternal parents. All the F1, F2 and double-cross populations were planted at distinct locations in different years, and the fertility-restoration reaction was scored by field investigation and pollen staining with I2-IK. The results were as follows: 1) The same test line could restore the CMS-C line at a certain genetic background, but failed to restore the CMS-C line at the other genetic backgrounds, suggesting that the genetic background of CMS-C lines plays an important role in the fertility restoration. 2) The fertile-to-sterile segregation ratio of (C48-2×A619) F2 population planted in both Sichuan and Yunnan fited well to 15∶1 by the χ 2 test. However, the fertility level of individuals in Yunnan mainly belonged to the Ⅲ and Ⅳgrades, but which in Sichuan mainly belonged to the Ⅴ grade, indicating the environmental factors had effect on the fertility-restoration reaction of (C48-2×A619) F2. 3) In our study, 18 bai could not restore C478, and 48-2 could not restore C478, but the fertile and sterile segregated plants were unexpectedly found in their double-cross population [(C478×18 bai) F1S×(C48-2×18 bai) F1F]. The similar case was also observed in the double-cross population [(C48-2 × zi 330) F1S × (C478 × zi 330) F1F]. Therefore, we speculated that there are minor fertility restorer genes not only in the nuclear background of C48-2 and C478, but also in zi 330 and 18 bai, and when these minor genes were gathered by hybridization, they could restore the fertility of C478 and C48-2. This conforms to the restorer genes dose-effect for fertility restoration in the plant CMS system. These results not only contribute to our understanding of the complexity and diversity of CMS-C restoration mechanism, but also provide an important reference for the practical applications about maize CMS-C.
Key words: maize; CMS-C; fertility restoration; double-cross populations
| [1] | Chen LT, Liu YG . Male sterility and fertility restoration in crops. Annu Rev Plant Biol, 2014,65(1):579-606. | |||
| [2] | Beckett JB . Classification of male-sterile cytoplasms in maize (Zea mays L.). Crop Sci, 1971,11(5):724-727. | |||
| [3] | Zheng YL . Study on the mechanism of the fertility about several types of cytoplasmic male-sterility in maize. J Huazhong Agric College, 1982, ( 1):44-68. | |||
| [3] | 郑用琏 . 若干玉米细胞质雄性不育类型(CMS)育性机理的研究. 华中农学院学报, 1982, ( 1):44-68. | |||
| [4] | Scheifele GL, Nelson RR, Koons C . Male sterility cytoplasm conditioning susceptibility of resistant inbred lines of maize to yellow leaf blight caused by Phyllosticta zeae. Plant Dis Rep, 1969,53:656-659. | |||
| [5] | Feng Y, Zheng Q, Song H, Wang Y, Wang H, Jiang LJ, Yan JB, Zheng YL, Yue B . Multiple loci not only Rf3 involved in the restoration ability of pollen fertility, anther exsertion and pollen shedding to S type cytoplasmic male sterile in maize. Theor Appl Genet, 2015,128(11):2341-2350. | |||
| [6] | 侯玮, 陈举林, 王国胜, 闫保罗, 李平海 . 细胞质雄性不育在玉米育种及生产中的应用概述. 安徽农学通报, 2011,17(1):64-66. | |||
| [7] | Sun QQ, Rong TZ . Study and use of cytoplasmic male sterility in maize. J Sichuan Agric Univ, 2003,21(1):49-53. | |||
| [7] | 孙庆泉, 荣廷昭 . 玉米胞质雄性不育材料的研究和利用. 四川农业大学学报, 2003,21(1):49-53. | |||
| [8] | 李继耕 . 细胞质雄性不育性的分子机理. 遗传, 1992,14(2):37-40. | |||
| [9] | Li DD, Wang B . Rice atpA gene cloning and relationship with cutoplasimic male sterility. Hereditas (Beijing), 1990,12(4):1-4. | |||
| [9] | 李大东, 王斌 . 水稻线粒体atpA基因的克隆及其与细胞质雄性不育的关系. 遗传, 1990,12(4):1-4. | |||
| [10] | Li XM, Zheng YL, Zhang FD, Zhu YG . RFLP analysis for mitochondria genome of CMS rice Honglian type. Hereditas (Beijing), 2000,22(4):201-204. | |||
| [10] | 李小明, 郑用琏, 张方东, 朱英国 . 红莲型细胞质雄性不育水稻线粒体DNA的RFLP分析. 遗传, 2000,22(4):201-204. | |||
| [11] | Dewey RE, Timothy DH, Levings III CS . Chimeric mitochondrial genes expressed in the C male-sterile cytoplasm of maize. Curr Genet, 1991,20(6):475-482. | |||
| [12] | Luo DP, Xu H, Liu ZL, Guo JX, Li HY, Chen LT, Fang C, Zhang QY, Bai M, Yao N, Wu H, Wu H, Ji CH, Zheng HQ, Chen YL, Ye S, Li XY, Zhao XC, Li RQ, Liu YG . A detrimental mitochondrial-nuclear interaction causes cytoplasmic male sterility in rice. Nat Genet, 2013,45(5):573-577. | |||
| [13] | Kazama T, Toriyama K . A pentatricopeptide repeat-containing gene that promotes the processing of aberrant atp6 RNA of cytoplasmic male-sterile rice. FEBS Lett, 2003,544(1-3):99-102.
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