Soybean cyst nematode （SCN Heterodera glycines Ichinohe） is one of the most important nationwide soybean diseases in China. A total of 38 soil specimens or locations in the area was sampled and tested for SCN races ...Soybean cyst nematode （SCN Heterodera glycines Ichinohe） is one of the most important nationwide soybean diseases in China. A total of 38 soil specimens or locations in the area was sampled and tested for SCN races during 2001-2003 for the inspection of race distribution in Huang-Huai Valleys. A map of race distribution was constructed according to the data from both the present study and the published reports cited. Three areas, namely, the area of southeast to Jinan in Shangdong Province; the area of northern Henan Province and its border region to south of Hebei Province; and the area of Luohe, Zhoukou of Henan Province and Fuyang of Anhui Province mainly infested with Race 1 were identified. Race 4 was predominant in Shanxi Province, Beijing and the adjacent area of Henan, Shandong, and Anhui provinces, and the delta of Huanghe River in Shandong Province. Race 2 was mainly found in Liaocheng, Dezhou of Shangdong Province and Shijiazhuang of Hebei Province, and Jiaozuo and Huojia of Henan Province. Race 7 was distributed in the west part of Jiaodong Peninsula of Shandong Province and Kaifeng, Huaxian, Wenxian of Henan Province. Race 5 was found and scattered in Hebei and Henan Province. Race 9 was found in Shangqiu of Henan Province, which was reported for the first time in China. It can be seen that Race 1 and Race 4 were the two predominant races in Huang-Huai Valleys, and that research should focus on developing resistant cultivars of these races. There might exist other races in an area with some predominant races. The race substitution in the past decade was not obviously found, therefore, the results should be meaningful to future breeding for resistance to SCN in Huang-Huai Valleys.展开更多
Soybean cyst nematode(SCN)Heterodera glycines is considered as the major constraint to soybean production.Gm SHMT08 at Rhg4 locus on chromosome 08,encoding a serine hydroxylmethyltransferase,is a major gene underlying...Soybean cyst nematode(SCN)Heterodera glycines is considered as the major constraint to soybean production.Gm SHMT08 at Rhg4 locus on chromosome 08,encoding a serine hydroxylmethyltransferase,is a major gene underlying resistance against H.glycines in Peking-type soybeans.However,the molecular mechanism underpinning this resistance is less well characterized,and whether Gm SHMT08 could interact with proteins in H.glycines remains unclear.In this study,yeast two-hybrid screening was conducted using Gm SHMT08 as a bait protein,and a fragment of a 70-kDa heat shock protein(Hg HSP70)was screened from H.glycines that exhibited interaction with Gm SHMT08.This interaction was verified by both GST pull-down and bimolecular fluorescence complementation assays.Our finding reveals Hg HSP70 could be applied as a potential candidate gene for further exploring the mechanism on Gm SHMT08-mediated resistance against SCN H.glycines.展开更多
Soybean cyst nematode(SCN,Heterodera glycines Ichinohe)is the most economically damaging disease of soybean worldwide,and breeding host plant resistance is the most feasible option for SCN management.In this review,we...Soybean cyst nematode(SCN,Heterodera glycines Ichinohe)is the most economically damaging disease of soybean worldwide,and breeding host plant resistance is the most feasible option for SCN management.In this review,we summarise the progress made so far in identifying nematode-resistance genes,the currently available sources of resistance,possible mechanisms of SCN resistance and strategies for soybean breeding.To date,only two sources of SCN resistance have been widely used,from the accessions PI 88788 and Peking,which has resulted in a shift in SCN resistance and created a narrow genetic base for SCN resistance.These resistant germplasms for SCN are classified into two types according to their copy number variation in a 31-kb genomic region:PI 88788-type resistance requires high copy numbers of a rhg1 resistance allele(rhg1-b)and Peking-type resistance requires both low copy numbers of a different rhg1 resistance allele(rhg1-a)and a resistant allele at another locus,Rhg4.Resistance related to rhg1 primarily involves impairment of vesicle trafficking through disruption of soluble NSF-attachment protein receptor(SNARE)complexes.By contrast,resistance via Rhg4 involves disturbance of folate homeostasis at SCN feeding sites due to alteration of the enzymatic activity of serine hydroxymethyltransferase(SHMT).Other potential mechanisms,including plant defences mediated by salicylic acid(SA)and jasmonic acid(JA)signalling modulation,have also been suggested for SCN resistance.Indeed,genome-wide association studies(GWAS)have identified other candidate SCN resistance genes,such as Gm SNAP11.Although gene functional analysis in a transient expression system could increase the efficiency of candidate gene identification,information on novel genes and mechanisms for SCN resistance remains limited.Any beneficial candidate genes identified might,when fully exploited,be valuable for improving the efficiency of marker-assisted breeding and dissecting the molecular mechanisms underlying SCN resistance.展开更多
大豆胞囊线虫1号和4号生理小种是黄淮地区的优势小种，ZDD2315是我国特优抗源。本文旨在定位ZDD2315对1号和4号生理小种抗性的QTL。试验以Essex为母本，ZDD2315为父本和轮回亲本，创建了一个包含114个单株的Bc。群体。采用250个SSR标记...大豆胞囊线虫1号和4号生理小种是黄淮地区的优势小种，ZDD2315是我国特优抗源。本文旨在定位ZDD2315对1号和4号生理小种抗性的QTL。试验以Essex为母本，ZDD2315为父本和轮回亲本，创建了一个包含114个单株的Bc。群体。采用250个SSR标记和1个形态标记通过MAPMAKER3．0构建了包含25个连锁群的遗传图谱，覆盖大豆基因组2963．5cM，平均每个连锁群上10．0个标记，标记平均间距11．8cM。采用Win QTL Cartographer Version 2．5复合区间作图法（CIM）检测到3个抗1号小种的QTL；其中rhgR1-1和rhgR1—2位于G连锁群的Sat_210～Sat_168和Sat_168～Sat_141区间，贡献率分别为22．4％和21.8％；rhgR1-3位于D2连锁群的Satt672～Satt413区间，贡献率6．2％；rhgR1-1和rhgR1—3分别与Sat_210和Satt672共分离。5个QTL与抗4号生理小种有关；其中rhgR4—1和rhgR4—-位于G连锁群的Satt275～Sat_210和Sat_168～Sat_141区间，贡献率分别为22．8％和28．9％；rhgR4—3和rhgR4—4位于H连锁群Satt442～Sat401和Sat_334～Satt181区间，贡献率分别为12．0％和10．5％；rhgR4—5位于L连锁群Satt652～Sat_301区间，贡献率5．9％；吨职4—2和rhgR4—5分别与Sat_168和Satt652共分离。不同遗传体系控制ZDD2315对1号和4号小种的抗性。抗1号和4号生理小种的主要QTL位于G连锁群的相近区段，且具有较大贡献率，通过标记辅助选择有可能育成兼抗两小种的品种。展开更多
To gain insight into the changes in the transcriptome of soybean roots during soybean cyst nematode (SCN) infection, we conducted genome-wide gene expression profiling using serial analysis of gene expression (SAGE) c...To gain insight into the changes in the transcriptome of soybean roots during soybean cyst nematode (SCN) infection, we conducted genome-wide gene expression profiling using serial analysis of gene expression (SAGE) combined with Solexa sequencing. More than 3 million tags were generated from the SCN-infected and uninfected roots, and 366941 and 314591 clean UniTags were obtained from SCN-infected and uninfected samples, respectively. In the SCN-infected sample, 48249 UniTags represented 18114 reference genes. In the uninfected control, 46290 UniTags represented 19323 reference genes. Comparison of tag frequencies identified 1405 genes that were expressed at greater levels in SCN-infected roots than in uninfected roots, and 1191 genes that were expressed at lower levels. Quantitative real-time PCR analyses confirmed the changes in mRNA levels observed in our sequencing analyses. A comparable number of genes were upand down-regulated in response to nematode infection, indicating that down-regulation of some genes might be essential in the plant response to nematodes. Our SAGE results showed significant changes in expression of many unreported genes involved in nematode infection. Approximately 7% of tags mapped to the antisense strand of genes, indicating widespread antisense transcription.展开更多
基金The project was supported by the National Natural Science Foundation of China （30490250）the National Key Basic Research Program （2002CB 111304, 2004CB7206）+1 种基金the National 863 Program （2002AA211052）the Program for Changjiang Scholars and Innovative Research Team in University （PCSIRT）.
文摘Soybean cyst nematode （SCN Heterodera glycines Ichinohe） is one of the most important nationwide soybean diseases in China. A total of 38 soil specimens or locations in the area was sampled and tested for SCN races during 2001-2003 for the inspection of race distribution in Huang-Huai Valleys. A map of race distribution was constructed according to the data from both the present study and the published reports cited. Three areas, namely, the area of southeast to Jinan in Shangdong Province; the area of northern Henan Province and its border region to south of Hebei Province; and the area of Luohe, Zhoukou of Henan Province and Fuyang of Anhui Province mainly infested with Race 1 were identified. Race 4 was predominant in Shanxi Province, Beijing and the adjacent area of Henan, Shandong, and Anhui provinces, and the delta of Huanghe River in Shandong Province. Race 2 was mainly found in Liaocheng, Dezhou of Shangdong Province and Shijiazhuang of Hebei Province, and Jiaozuo and Huojia of Henan Province. Race 7 was distributed in the west part of Jiaodong Peninsula of Shandong Province and Kaifeng, Huaxian, Wenxian of Henan Province. Race 5 was found and scattered in Hebei and Henan Province. Race 9 was found in Shangqiu of Henan Province, which was reported for the first time in China. It can be seen that Race 1 and Race 4 were the two predominant races in Huang-Huai Valleys, and that research should focus on developing resistant cultivars of these races. There might exist other races in an area with some predominant races. The race substitution in the past decade was not obviously found, therefore, the results should be meaningful to future breeding for resistance to SCN in Huang-Huai Valleys.
基金supported by the National Natural Science Foundation of China(31972248)the Agricultural Science and Technology Innovation Project of Chinese Academy of Agricultural Sciences,China(ASTIP-02IPP-04)。
文摘Soybean cyst nematode(SCN)Heterodera glycines is considered as the major constraint to soybean production.Gm SHMT08 at Rhg4 locus on chromosome 08,encoding a serine hydroxylmethyltransferase,is a major gene underlying resistance against H.glycines in Peking-type soybeans.However,the molecular mechanism underpinning this resistance is less well characterized,and whether Gm SHMT08 could interact with proteins in H.glycines remains unclear.In this study,yeast two-hybrid screening was conducted using Gm SHMT08 as a bait protein,and a fragment of a 70-kDa heat shock protein(Hg HSP70)was screened from H.glycines that exhibited interaction with Gm SHMT08.This interaction was verified by both GST pull-down and bimolecular fluorescence complementation assays.Our finding reveals Hg HSP70 could be applied as a potential candidate gene for further exploring the mechanism on Gm SHMT08-mediated resistance against SCN H.glycines.
基金supported by the National Key Research and Development Program of China(2016YFD0100504,2016YFD0100201,and 2017YFD0101400)the National Natural Science Foundation of China(No.31301345 and No.31671716)+1 种基金the National Major Science and Technology Project of China(2016ZX08004-003)the Agricultural Science and Technology Innovation Program of CAAS。
文摘Soybean cyst nematode(SCN,Heterodera glycines Ichinohe)is the most economically damaging disease of soybean worldwide,and breeding host plant resistance is the most feasible option for SCN management.In this review,we summarise the progress made so far in identifying nematode-resistance genes,the currently available sources of resistance,possible mechanisms of SCN resistance and strategies for soybean breeding.To date,only two sources of SCN resistance have been widely used,from the accessions PI 88788 and Peking,which has resulted in a shift in SCN resistance and created a narrow genetic base for SCN resistance.These resistant germplasms for SCN are classified into two types according to their copy number variation in a 31-kb genomic region:PI 88788-type resistance requires high copy numbers of a rhg1 resistance allele(rhg1-b)and Peking-type resistance requires both low copy numbers of a different rhg1 resistance allele(rhg1-a)and a resistant allele at another locus,Rhg4.Resistance related to rhg1 primarily involves impairment of vesicle trafficking through disruption of soluble NSF-attachment protein receptor(SNARE)complexes.By contrast,resistance via Rhg4 involves disturbance of folate homeostasis at SCN feeding sites due to alteration of the enzymatic activity of serine hydroxymethyltransferase(SHMT).Other potential mechanisms,including plant defences mediated by salicylic acid(SA)and jasmonic acid(JA)signalling modulation,have also been suggested for SCN resistance.Indeed,genome-wide association studies(GWAS)have identified other candidate SCN resistance genes,such as Gm SNAP11.Although gene functional analysis in a transient expression system could increase the efficiency of candidate gene identification,information on novel genes and mechanisms for SCN resistance remains limited.Any beneficial candidate genes identified might,when fully exploited,be valuable for improving the efficiency of marker-assisted breeding and dissecting the molecular mechanisms underlying SCN resistance.
文摘大豆胞囊线虫1号和4号生理小种是黄淮地区的优势小种，ZDD2315是我国特优抗源。本文旨在定位ZDD2315对1号和4号生理小种抗性的QTL。试验以Essex为母本，ZDD2315为父本和轮回亲本，创建了一个包含114个单株的Bc。群体。采用250个SSR标记和1个形态标记通过MAPMAKER3．0构建了包含25个连锁群的遗传图谱，覆盖大豆基因组2963．5cM，平均每个连锁群上10．0个标记，标记平均间距11．8cM。采用Win QTL Cartographer Version 2．5复合区间作图法（CIM）检测到3个抗1号小种的QTL；其中rhgR1-1和rhgR1—2位于G连锁群的Sat_210～Sat_168和Sat_168～Sat_141区间，贡献率分别为22．4％和21.8％；rhgR1-3位于D2连锁群的Satt672～Satt413区间，贡献率6．2％；rhgR1-1和rhgR1—3分别与Sat_210和Satt672共分离。5个QTL与抗4号生理小种有关；其中rhgR4—1和rhgR4—-位于G连锁群的Satt275～Sat_210和Sat_168～Sat_141区间，贡献率分别为22．8％和28．9％；rhgR4—3和rhgR4—4位于H连锁群Satt442～Sat401和Sat_334～Satt181区间，贡献率分别为12．0％和10．5％；rhgR4—5位于L连锁群Satt652～Sat_301区间，贡献率5．9％；吨职4—2和rhgR4—5分别与Sat_168和Satt652共分离。不同遗传体系控制ZDD2315对1号和4号小种的抗性。抗1号和4号生理小种的主要QTL位于G连锁群的相近区段，且具有较大贡献率，通过标记辅助选择有可能育成兼抗两小种的品种。
基金supported by the National Natural Science Foundation of China (30392100)
文摘To gain insight into the changes in the transcriptome of soybean roots during soybean cyst nematode (SCN) infection, we conducted genome-wide gene expression profiling using serial analysis of gene expression (SAGE) combined with Solexa sequencing. More than 3 million tags were generated from the SCN-infected and uninfected roots, and 366941 and 314591 clean UniTags were obtained from SCN-infected and uninfected samples, respectively. In the SCN-infected sample, 48249 UniTags represented 18114 reference genes. In the uninfected control, 46290 UniTags represented 19323 reference genes. Comparison of tag frequencies identified 1405 genes that were expressed at greater levels in SCN-infected roots than in uninfected roots, and 1191 genes that were expressed at lower levels. Quantitative real-time PCR analyses confirmed the changes in mRNA levels observed in our sequencing analyses. A comparable number of genes were upand down-regulated in response to nematode infection, indicating that down-regulation of some genes might be essential in the plant response to nematodes. Our SAGE results showed significant changes in expression of many unreported genes involved in nematode infection. Approximately 7% of tags mapped to the antisense strand of genes, indicating widespread antisense transcription.
