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一个具有抗条锈病特性的新型小麦-羊草Lm#7Ns(7D)二体代换系的创制与分子细胞遗传学鉴定

Development and Molecular Cytogenetic Identification of a Novel Wheat-Leymus mollis Lm#7Ns (7D) Disomic Substitution Line with Stripe Rust Resistance.

作者信息

Yang Xiaofei, Wang Changyou, Li Xin, Chen Chunhuan, Tian Zengrong, Wang Yajuan, Ji Wanquan

机构信息

College of Agronomy, State Key Laboratory of Crop Stress Biology for Arid Areas, Northwest A & F University, Yangling, Shaanxi, 712100, China.

出版信息

PLoS One. 2015 Oct 14;10(10):e0140227. doi: 10.1371/journal.pone.0140227. eCollection 2015.

DOI:10.1371/journal.pone.0140227
PMID:26465140
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4605682/
Abstract

Leymus mollis (2n = 4x = 28, NsNsXmXm) possesses novel and important genes for resistance against multi-fungal diseases. The development of new wheat-L. mollis introgression lines is of great significance for wheat disease resistance breeding. M11003-3-1-15-8, a novel disomic substitution line of common wheat cv. 7182 -L. mollis, developed and selected from the BC1F5 progeny between wheat cv. 7182 and octoploid Tritileymus M47 (2n = 8x = 56, AABBDDNsNs), was characterized by morphological and cytogenetic identification, analysis of functional molecular markers, genomic in situ hybridization (GISH), sequential fluorescence in situ hybridization (FISH)-genomic in situ hybridization (GISH) and disease resistance evaluation. Cytological observations suggested that M11003-3-1-15-8 contained 42 chromosomes and formed 21 bivalents at meiotic metaphase I. The GISH investigations showed that line contained 40 wheat chromosomes and a pair of L. mollis chromosomes. EST-STS multiple loci markers and PLUG (PCR-based Landmark Unique Gene) markers confirmed that the introduced L. mollis chromosomes belonged to homoeologous group 7, it was designated as Lm#7Ns. While nulli-tetrasomic and sequential FISH-GISH analysis using the oligonucleotide Oligo-pSc119.2 and Oligo-pTa535 as probes revealed that the wheat 7D chromosomes were absent in M11003-3-1-15-8. Therefore, it was deduced that M11003-3-1-15-8 was a wheat-L. mollis Lm#7Ns (7D) disomic substitution line. Field disease resistance demonstrated that the introduced L. mollis chromosomes Lm#7Ns were responsible for the stripe rust resistance at the adult stage. Moreover, M11003-3-1-15-8 had a superior numbers of florets. The novel disomic substitution line M11003-3-1-15-8, could be exploited as an important genetic material in wheat resistance breeding programs and genetic resources.

摘要

滨麦(2n = 4x = 28,NsNsXmXm)拥有抗多种真菌病害的新的重要基因。培育新的小麦-滨麦渐渗系对小麦抗病育种具有重要意义。M11003-3-1-15-8是普通小麦品种7182-滨麦的一个新型二体代换系,它是从小麦品种7182与八倍体小滨麦M47(2n = 8x = 56,AABBDDNsNs)的BC1F5后代中选育出来的,通过形态学和细胞遗传学鉴定、功能分子标记分析、基因组原位杂交(GISH)、顺序荧光原位杂交(FISH)-基因组原位杂交(GISH)以及抗病性评价对其进行了特征描述。细胞学观察表明,M11003-3-1-15-8含有42条染色体,在减数分裂中期I形成21个二价体。GISH研究表明,该品系含有40条小麦染色体和一对滨麦染色体。EST-STS多位点标记和PLUG(基于PCR的地标独特基因)标记证实,导入的滨麦染色体属于第7同源群,被命名为Lm#7Ns。而使用寡核苷酸Oligo-pSc119.2和Oligo-pTa535作为探针的缺体-四体和顺序FISH-GISH分析表明,M11003-3-1-15-8中没有小麦7D染色体。因此,推断M11003-3-1-15-8是一个小麦-滨麦Lm#7Ns(7D)二体代换系。田间抗病性表明,导入的滨麦染色体Lm#7Ns对成株期条锈病具有抗性。此外,M11003-3-1-15-8的小花数量较多。新型二体代换系M11003-3-1-15-8可作为小麦抗病育种项目中的重要遗传材料和遗传资源加以利用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cfc/4605682/7ca51587851b/pone.0140227.g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cfc/4605682/2a7ac9727147/pone.0140227.g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cfc/4605682/01ebc1fd6592/pone.0140227.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cfc/4605682/2d97c4d70716/pone.0140227.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cfc/4605682/c813bfef941b/pone.0140227.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cfc/4605682/ea027cc557be/pone.0140227.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cfc/4605682/37ef5f7b037c/pone.0140227.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cfc/4605682/4469d0baac8e/pone.0140227.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cfc/4605682/7ca51587851b/pone.0140227.g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cfc/4605682/2a7ac9727147/pone.0140227.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cfc/4605682/48875fc26af3/pone.0140227.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cfc/4605682/01ebc1fd6592/pone.0140227.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cfc/4605682/2d97c4d70716/pone.0140227.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cfc/4605682/c813bfef941b/pone.0140227.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cfc/4605682/ea027cc557be/pone.0140227.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cfc/4605682/37ef5f7b037c/pone.0140227.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cfc/4605682/4469d0baac8e/pone.0140227.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cfc/4605682/7ca51587851b/pone.0140227.g009.jpg

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