Ultrastructural Changes in the Interaction Between Puccinia striiformis and Wheat Cultivar with Slow-Rusting Resistance

Ultrastructural changes in both pathogen and host cells in the interaction between Puccinia striiformis and wheat cultivar （Libellula） with slow-rusting resistance were observed by transmission electron microscopy. Observations revealed marked changes in ultrastructure of both pathogen and host cells. In the pathogen respect, there were many vesicles appeared in the intercellular hyphae and gradually fused into bigger vacuoles, a number of fat drops and electron-dense granules accumulated, mitochondria became swollen and some of them degraded into vesicles, and the plasmalemma of intercellular hyphae became dark. In the haustoria, the cytoplasm degraded gradually and developed a vacuole in the center, fat drops increased, the extrahaustorial matrix widened with a great amount of electron-dense fibrillar and granular materials, and most of the haustoria died with in conjunction with the disappearance of fat drops and other organelles. Structural defense of the host, including formation of cell wall apposition, collar and papilla, occurred in the host respect. Host resistance expression and cytological features occurring in the slow-rusting resistance were discussed.

The TaFIM1 gene mediates wheat resistance against Puccinia striiformis f. sp. tritici and responds to abiotic stress

Fimbrin, a regulator of actin cytoskeletal dynamics that participates in numerous physiological and biochemical processes, controls multiple developmental processes in a variety of tissues and cell types. However, the role of fimbrin in pathogen defense of wheat and the mechanisms have not been well studied. Here, we investigated that the expression of TaFIM1 gene of wheat was significantly induced in response to avirulent race of Puccinia striiformis f. sp. tritici(Pst) and silencing of TaFIM1 by virus-induced gene silencing method. The results show that silencing of TaFIM1 resulted in a reduction of resistance against the stripe rust indicated by both phenotypes and a histological examination of Pst growth. Additionally, the expression level of Ta FIM1 gene was up-regulated under abiotic stresses. These findings suggest that Ta FIM1 functions as a positive regulator of pathogen resistance of wheat plants and response to abiotic stress. Our work may show new light on understanding the roles of fimbrin in wheat.

Study of the Adult-Plant Resistance at Different Growth Stages to Stripe Rust in Wheat

Components of resistance were investigated for five adult-plant resistant (APR) wheat (Triticum aestivum) cultivars at sixgrowth stages and two temperatures in the greenhouse, and disease progress in a field trial. Chinese cultivar Chuanyu 12displayed high to intermediate infection type (IT) in the greenhouse but was highly resistant in the field. Weebill showedan intermediate IT in the greenhouse and also in the field. Chpaio, Tukuru and Saar, known to carry combinations of Yr18and 2-3 additional minor genes, were highly resistant in both experiments. Greenhouse experiments indicated that thelower IT of APR cultivars initiated at tillering stage. Latent periods (LP) for APR cultivars were generally longer as thegrowth stage progressed. We conclude that APR to stripe rust can be best characterized in field trials although significantcorrelations are seen between field severity and IT and LP measured in the greenhouse.

Characterization of a 4.1 Mb inversion harboring the stripe rust resistance gene YR86 on wheat chromosome 2AL

Wheat cultivar Zhongmai 895 was earlier found to carry YR86 in an 11.6 Mb recombination-suppressed region on chromosome 2AL when crossed with Yangmai 16.To fine-map the YR86 locus,we developed two large F2 populations from crosses Emai 580/Zhongmai 895 and Avocet S/Zhongmai 895.Remarkably,both populations exhibited suppressed recombination in the same 2AL region.Collinearity analysis across Chinese Spring,Aikang 58,and 10+wheat genomes revealed a 4.1 Mb chromosomal inversion spanning 708.5-712.6 Mb in the Chinese Spring reference genome.Molecular markers were developed in the breakpoint and were used to assess a wheat cultivar panel,revealing that Chinese Spring,Zhongmai 895,and Jimai 22 shared a common sequence named InvCS,whereas Aikang 58,Yangmai 16,Emai 580,and Avocet S shared the sequence named InvAK58.The inverted configuration explained the suppressed recombination observed in all three bi-parental populations.Normal recombination was observed in a Jimai 22/Zhongmai 895 F2 population,facilitating mapping of YR86 to a genetic interval of 0.15 cM corresponding to 710.27-712.56 Mb falling within the inverted region.Thirty-three high-confidence genes were annotated in the interval using the Chinese Spring reference genome,with six identified as potential candidates for YR86 based on genome and transcriptome analyses.These results will accelerate map-based cloning of YR86 and its deployment in wheat breeding.

Mapping of a Major Stripe Rust Resistance Gene in Chinese Native Wheat Variety Chike Using Microsatellite Markers

Chike （accession number Su1900）, a Chinese native wheat （Triticum aestivum L.） variety, is resistant to the currently prevailing physiological races of Puccinia striiformis Westend. f. sp. tritici in China. Genetic analysis indicated that resistance to the physiological race CY32 of the pathogen in the variety was controlled by one dominant gene. In this study, BSA （bulked segregant analysis） methods and SSRs （simple sequence repeats） marker polymorphic analysis are used to map the gene. The resistant and susceptible DNA bulks were prepared from the segregating F2 population of the cross between Taichung 29, a susceptible variety as maternal parent, and Chike as paternal parent. Over 400 SSR primers were screened, and five SSR markers Xwmc44, Xgwm259, Xwmc367, Xcfa2292, and Xbarc80 on the chromosome arm 1BL were found to be polymorphic between the resistant and the susceptible DNA bulks as well as their parents. Genetic linkage was tested on segregating F2 population with 200 plants, including 140 resistant and 60 susceptible plants. All the five SSR markers were linked to the stripe rust resistance gene in Chike. The genetic distances for the markers Xwmc44, Xgwm259, Xwmc367, Xcfa2292, and Xbarc80 to the target gene were 8.3 cM, 9.1 cM, 17.2 cM, 20.6 cM, and 31.6 cM, respectively. Analysis using 21 nulli-tetrasomic Chinese Spring lines further confirmed that all the five markers were located on chromosome lB. On the basis of the above results, it is reasonable to assume that the major stripe rust resistance gene YrChk in Chike was located on the chromosome arm 1BL, and its comparison with the other stripe rust resistance genes located on 1B suggested that YrChk may be a novel gene that provides the resistance against stripe rust in Chike. Exploration and utilization of resources of disease resistance genes in native wheat varieties will be helpful both to diversify the resistance genes and to amend the situation of resistance gene simplification in the commercial wheat cultivars in China.

Genetic Analysis and Molecular Mapping of a Stripe Rust Resistance Gene YrH9014 in Wheat Line H9014-14-4-6-1

Stripe rust, caused by Puccinia striiformis f. sp. tritici （Pst）, is one of the most widespread and destructive wheat diseases in many wheat-growing regions of the world. The winter wheat translocation line H9014-14-4-6-1 has all stage resistance. To identify stripe rust resistance genes, the segregating populations were developed from the cross between H9014-14-4-6-1 and Mingxian 169 （a wheat cultivar susceptible to all Pst races identified in China）. The seedlings of the parents and F1 plants, Fz, F3 and BC1 generations were tested with Pst races under controlled greenhouse conditions. Two genes for resistance to stripe rust were identified, one dominant gene conferred resistance to SUN11-4, temporarily designated YrH9014 and the other recessive gene conferred resistance to CYR33. The bulked segregant analysis and simple sequence repeat （SSR） markers were used to identify polymorphic markers associated with YrH9014. Seven polymorphic SSR markers were used to genotype the F2 population inoculated with SUN11-4. A linkage map was constructed according to the genotypes of seven SSR markers and resistance gene. The molecular map spanned 24.3 cM, and the genetic distance of the two closest markers Xbarc13 and Xbarc55 to gene locus was 1.4 and 3.6 cM, respectively. Based on the position of SSR marker, the resistance gene YrH9014 was located on chromosome arm 2BS. Amplification of a set of nulli-tetrasomic Chinese Spring lines with SSR marker Xbarc13 indicated that YrH9014 was located on chromosome 2B. Based on chromosomal location, the reaction patterns and pedigree analysis, YrH9014 should be a novel resistance gene to stripe rust. This new gene and flanking markers got from this study should be useful for marker-assisted selection （MAS） in breeding programs for stripe rust.

Characterization and Molecular Mapping of a Stripe Rust Resistance Gene in Synthetic Wheat CI110

Stripe rust,caused by Puccinia striiformis f.sp.tritici（Pst）,is one of the most destructive diseases of wheat（Triticum aestivum L.）.To diversify stripe rust-resistant resources for wheat breeding programs,a CIMMYT synthetic wheat line CI110 was identified to be resistant to 28 isolates of Pst,including 6 Chinese prevalent races CYR28-CYR33.Genetic analysis indicated that a single dominant gene was responsible for the stripe rust resistance in CI110,temporarily designated YrC110.A molecular map,harboring YrC110 and 9 linked SSR markers,was constructed through simple sequence repeat（SSR）,and bulked segregant analysis.These linked markers and YrC110 were assigned on the short arm of chromosome 1B using the Chinese Spring nullisomic-tetrasomic and ditelosomic stocks.Gene postulation based on seedling reaction patterns to 30 Pst isolates suggested that the resistance gene YrC110 seemed different from the other known resistance genes tested,such as Yr9,Yr10,Yr15,Yr24,and Yr26/YrCH42.Four SSR markers Xbarc187150,Xgwm18227,Xgwm11223,and Xbarc240292 distinguished YrC110 from Yr10,Yr15,Yr24,and Yr26/YrCH42,and could be used as diagnostic ones for YrC110 in wheat resistant breeding programs against stripe rust.

Three co-located resistance genes confer resistance to leaf rust and stripe rust in wheat variety Borlaug 100

Leaf rust(LR) and stripe rust(YR) are important diseases in wheat producing areas worldwide and cause severe yield losses under favorable environmental conditions when susceptible varieties are grown. We determined the genetic basis of resistance to LR and YR in variety Borlaug 100 by developing and phenotyping a population of 198 F6 recombinant inbred lines derived from a cross with the susceptible parent Apav#1. LR and YR phenotyping were conducted for 4 and 3 seasons, respectively, at CIMMYT research stations in Mexico under artificial epidemics. Mendelian segregation analyses indicated that 3–5 LR and 2 YR genes conferred resistance in Borlaug 100. Lr46/Yr29(1 BL), Yr17(2 AS) and Yr30(3 BS) were present in the resistant parent and segregated in the RIL population based on characterization by molecular markers linked to these genes. When present alone, Lr46/Yr29 caused average 13% and 16% reductions in LR and YR severities, respectively, in RILs. Similarly, Yr17 and Yr30 reduced YR severities by 57% and 11%, respectively. The Yr30 and the Yr17 translocation were also associated with 27% and 14% reductions, respectively, in LR severity, indicating that the 3 BS and 2 AS chromosomal regions likely carry new slow rusting LR resistance genes, temporarily designated as Lr B1 and Lr B2, respectively. Additive effects of Yr30*Yr17, Yr29*Yr17 and Yr29*Yr30 on YR and LR were significant and reduced YR severities by 56%,55%, and 45%, respectively, and LR severities by 34%, 40%, and 45%, respectively. Furthermore, interaction between the three genes was also significant, with mean reductions of 70% for YR and 54% for LR severities. Borlaug 100, or any one of the 21 lines with variable agronomic traits but carrying all three colocated resistance loci, can be used as resistance sources in wheat breeding programs.

Molecular Mapping of a Gene for Resistance to Stripe Rust in Wheat Variety PIW138

Stripe rust, caused by Puccinia striiformis f. sp. tritici （Pst）, is one of the most damaging diseases of common wheat （Triticum aestivum L.）. Wheat variety PIW138 introduced from Pakistan is resistant to the currently prevailing Pst race CYR32 in China. In this study, the bulked segregant analysis （BSA） method and simple sequence repeat （SSR） markers were used to map the stripe rust resistance gene in PIW138. The resistant and susceptible DNA bulks were prepared from the segregating F2 population of the cross between Thatcher, a susceptible variety as the female parent, and PIW138 as the male parent. The segregation of resistant and susceptible F2 plants inoculated with CYR32 indicated that single dominant gene determined the reactions of PIW138 line and temporarily designated as YrP138. Total 200 SSR primers were screened, and 4 SSR markers, Xwmc52, Xbarc61, Xgwm268, and Xgwm153, on chromosome 1B were found to be polymorphic between the resistant and the susceptible DNA bulks as well as their parents. Genetic linkage was tested on the segregating F2 population with 259 plants, including 196 resistant and 63 susceptible plants. All 4 SSR markers were linked to the stripe rust resistance gene in PIW138. The genetic distances of Xwmc52, Xbarc61, Xgwm268, and Xgwm153 to the resistance gene were 29.8, 6.2, 6.8, and 8.2 cM, respectively.

Genetics and Molecular Mapping of Stripe Rust Resistance Gene YrShan515 in Chinese Wheat Cultivar Shan 515

Stripe rust is one of the most important wheat diseases worldwide. To identify new resistance genes is significant in wheat breeding. In this study, stripe rust resistance of a Chinese cultivar Shan 515 was tested with Chinese predominant races of P. striiformis f. sp. tritici in the seedling stage, and genetic analysis and simple sequence repeats （SSR） technique were used to identify the inheritance model of seedling stripe rust resistance in cultivar Shan 515 and to mark the sites of resistance gene（s） on chromosome. The genetic analysis indicated that the resistance of Shan 515 against Su11-4 was conferred by a single dominant gene, which was temporarily designated as YrShan515. Using bulked segregant analysis （BSA） and SSR markers, 12 SSR markers （Xwmc335, Xwmc696, Xwmc476, Xbarc267, Xgwm333, Xwmc653, Xwmc396, Xgwm213, Xgwm112, Xgwm274, Xcfd22, Xgwm131, and Xwmc517） located on wheat chromosome 7BL were linked to YrShan515 with genetic distance ranging from 3 to 24 cM. Based on the previously published genetic map and Chinese Spring nulli-tetrasomic analysis, YrShan515 was located on wheat chromosome 7BL. Polymorphism of wheat cultivars collected from Huanghuai wheat grown regions were screened with two markers, Xwmc653 and Xbarc267, and all of these wheat cultivars tested did not present the polymorphic bands as Shan 515 did. Therefore, it suggested that YrShan515 might be a allele of the available yellow rust resistance gene. The mapping of the new resistance gene in Shan 515 is useful for wheat breeding and diversification of resistance genes against stripe rust in commercial wheat cultivars in China.

Wheat Stripe Rust Virulence and Varietal Resistance in the Foot Hill Himalayas of Nepal

Stripe rust, caused by Puccinia striiformis f. sp. tritici （Pst） is an important disease of wheat （Triticum aestivum） in Nepal, which is a part of the Himalayas stretching over the North of Nepal, India, Pakistan, Bhutan and beyond. Wheat production plays a crucial role in food security of the marginal hill farmers of Nepal. Frequent epidemics of the rust have caused huge loss in farmer＇s field. Periodic monitoring during 1980-2008 showed that changes in virulence occurred during this period. The objective of this study was to evaluate Pst resistance and its effective genes in wheat genotypes. For this, trap nurseries, wheat stripe rust differentials, commercial cultivars and advanced breeding lines were tested under artificial epiphytotic and natural hot spots conditions during 2005 to 2010. Four genes （Yr5, Yr10, Yr15 and YrSp） consistently showed resistance to the prevailing races. The gene Yr9 and Yr27 in combinations with Yrl8 were found effective. Other lines with combination of minor genes were also found effective. The genotypes Amadina, Kukuna, Tukuru, Kakatsi and Buck Buck widely used in breeding program were resistant. The cultivation of varieties WK1204, Gautam, Gaura and Dhaulagiri have ensured genetic diversity for the rust resistance and slowed down frequent occurrence of epidemics. The findings of these studies could help in developing effective varietal resistance program in the sub-continent.

Genetic Analysis of Major and Minor Gene(s) Resistant to Stripe Rust in Important Resource Wheat Line Jinghe891-1

Inheritance of line Jinghe891-l resistant to pathotype of Puccinia striiformis in two patterns of temperature (Normal: day 18℃ /night 10℃ , High: day 24℃ /night 15℃ )was studied in this paper. The results showed that there were at least two pairs of dominant major genes and one pair of recessive minor genes in Jinghe 891-1. The two pairs of major genes that conferred resistance to CY31 were allelic or linked closely with resistance gene in Jubilejna Ⅱ , Kangyin655 and T. spelta Album. They were novel resistance genes and were inherited in a repeated or independent mode. The minor genes, which could modify the major genes, were sensitive to temperature and conferred resistance to all pathotypes of Puccinia striiformis in China. It is recommended that this line can be used as an important resource stock.

Genetic analysis of adult plant,quantitative resistance to stripe rust in wheat landrace Wudubaijian in multi-environment trials

Stripe rust,caused by Puccinia striiformis f.sp.tritici(Pst),is one of the most destructive diseases on wheat worldwide.Wudubaijian,a wheat landrace released from Gansu Province in China since 1950,exhibits adult-plant resistance to stripe rust for several decades.To elucidate the genetic basis of stripe rust resistance,Wudubaijian was crossed with the high susceptible cultivar Mingxian 169,and stripe rust tests of both parents and the F2:3 lines were conducted in four environments of Yangling and Tianshui in 2015 and 2016,respectively.The relative area under disease progress curve(rAUDPC)of Mingxian 169/Wudubaijian F_(2:3) lines showed that the resistance of Wudubaijian was controlled by quantitative trait loci(QTL).Combined with phenotypic data and molecular markers,two stable QTLs were identified in Wudubaijian.QYrwdbj.nwafu-5A with the phenotypic variance of 15.02-40.26% was located between 5AS1-0.40-0.75 and 5AS3-0.75-0.98 of chromosome 5AS,and QYrwdbj.nwafu-2B.1 with the phenotypic variance of 9.54-10.40%was located in the bin C-2BS1-0.53 of chromosome 2BS.Through the location of flanking markers and epistasis analysis,QYrwdbj.nwafu-5A may be a new major QTL that can be used in conjunction with other stripe rust resistance genes(QTLs).

Ultrastructure of Slow-Rusting Expression of Wheat to Stripe Rust

The ultrastructure of wheat cultivars with slow-rusting resistance expression to the stripe rust, Puccinia striiformis, wasstudied through TEM. The results show that slow-rusting has the same hypersensitive response characters with the lowinfection type resistance, but the mesophyll cell necrotized less in number, thereby only partially inhibiting the extensionof rust fungus, and the fungus being inhibited and necrosed slighter in degree. Apart from the occurrence ofhypersensitiveness, the response of the host cells in slow-rusting wheat cultivars to the infection of fungus also producesstructural materials associated with defense reaction, but distinctly less than that in resistant cultivar. Thus, it is suggestedthat the slow-rusting resistance might have a similar mechanism with the low infection type resistance of race specificity,but with lower intensity.

Reactions of Triticum urartu accessions to two races of the wheat yellow rust pathogen

Triticum urartu(AA,2n=2x=14),a wild grass endemic to the Fertile Crescent(FC),is the progenitor of the A subgenome in common wheat.It belongs to the primary gene pool for wheat improvement.Here,we evaluated the yellow rust(caused by Puccinia striiformis f.sp.tritici,Pst)reactions of 147 T.urartu accessions collected from different parts of the FC.The reactions varied from susceptibility to strong resistance.In general,there were more accessions with stronger resistance to race CYR33 than to CYR 32.In most cases the main form of defense was a moderate resistance characterized by the presence of necrotic/chlorotic lesions with fewer Pst uredinia on the leaves.Forty two accessions displayed resistance to both races.Histological analysis showed that Pst growth was abundant in the compatible interaction but significantly suppressed by the resistant response.Gene silencing mediated by Barley stripe mosaic virus was effective in two T.urartu accessions with different resistance responses,indicating that this method can expedite future functional analysis of resistance genes.Our data suggest that T.urartu is a valuable source of resistance to yellow rust,and represents a model for studying the genetic,genomic and molecular basis underlying interaction between wheat and Pst.

Identification of an AFLP marker linked to the stripe rust resistance gene Yr10 in wheat

AFLP analysis of near-isogenic lines of the stripe rust resistance gene Yr10 was carried out with 6 Pst I -primers and 10 Taq I -primers with the donor parent of Yr1O gene as the check. A total of about 4200 distinguishable bands were amplified, of which 5 were stable. The genetic linkage of the 5 polymorphic DNA fragments with the target gene were tested preliminarily on a segregating F2 population derived from a cross between the gene donor parent 'Moro' and susceptible cultivar 'Mingxian 169'. The DNA fragment PT0502 was found closely linked to the Yr10 gene and cloned and sequenced. Based on the sequence specific primers for PCR were designed and synthesized. Genetic linkage analysis with 195 segregating F2 plants indicated that the genetic distance was 0.5 cM between the main product SC200 fragment produced by PCR with the primers and the Yr10 gene. The primers can be used to detect the Yr10 gene quickly, effectively and exactly.

中国小麦抗条锈病基因育种利用现状与策略

小麦条锈病是中国重要的流行性真菌病害,严重威胁国家粮食安全。通过持续应用抗病品种和植保措施,小麦条锈病在中国得到了较好的控制。然而,随着全球气候变化、栽培制度的变革、育种方法技术的改进、产量水平的提高及条锈菌群体结构和毒性频率的不断变异,有必要对新时期小麦抗条锈病基因育种利用现状进行科学评估,以期为广谱持久多抗小麦品种的培育提供依据。本文通过对近年来中国西南、西北和黄淮主产区小麦品种(系)的条锈病抗性进行系统的抗病鉴定、遗传分析和抗条锈病基因分子标记的定位和检测,总结了中国小麦育种中主要抗条锈病基因的利用情况,对中国小麦抗条锈病基因发掘与种质创新、小麦育种中利用的主要抗条锈病基因、新时期抗条锈病基因利用的策略、小麦育种中抗条锈病基因选择和鉴定等进行了论述,并对新时期小麦抗条锈病育种发展方向进行了展望。

重要抗源京核8811品系抗小麦条锈病主效基因的单体分析

采用单体分析技术 ,用中国小麦条锈菌优势小种 CY31和埃塞俄比亚菌系 35E134的单孢菌系对重要抗源京核 8811品系进行抗条锈基因分析及定位。结果表明 :京核 8811含有抗 35E134菌系、位于 2 A染色体上和抗 CY31菌系、位于 4 D染色体上的两对显性抗条锈基因 ,二者均控制 0 - 0 ;的侵染型。异同比较显示 ,定位基因不同于国际上已定名的抗条锈基因 ,谓之新基因 ,暂定名为 Yr Jh1和Yr Jh2。 Yr Jh2具有比 Yr Jh1更宽的抗性谱 ,二者同时存在 ,使京核 8811具有较强的抗条锈性 ,抗中国目前所有小种 。

80份国外春小麦种质资源抗条锈性评价

【目的】小麦条锈病是由小麦条锈菌(Puccinia striiformis f.sp.tritici,Pst)引起的世界范围内小麦重要病害之一,培育和种植抗病品种是控制该病害的最有效策略。评价80份国外春小麦种质资源对中国当前小麦条锈菌流行小种的抗条锈性,为中国小麦抗条锈病育种提供依据和抗源。【方法】应用中国流行小麦条锈菌生理小种CYR29、CYR31、CYR32、CYR33以及致病类型PST-HY8和PST-V26对80份国外小麦种质资源进行苗期温室抗病性鉴定,以铭贤169和Av S为感病对照品种;并于2013年和2014年分别在陕西省杨凌和甘肃省天水进行田间成株期抗病性鉴定。根据苗期和田间成株期的抗病性鉴定结果对其进行抗病类型分类和评价。【结果】80份小麦种质资源的抗病类型可分为3类。第1类为全生育期抗病类型,有8份。其中PI660067、PI660119和PI660122在苗期和田间成株期均表现较高水平的抗病性。其余5个品系PI660056、PI607839、PI591045、TA5602和PI660064在苗期则对个别小种表现感病,并且在不同年份和不同测试地点成株期也表现感病。第2类为成株抗病类型,有28份。其苗期对所有测试小种均表现感病,有23份在田间成株期均表现抗病。但PI660075、PI660083、PI660085、PI660097和PI660107在不同年份和不同测试地点成株期表现感病。第3类为兼具成株期和对部分中国小种失去抗性的全生育期抗病类型,有44份,其苗期至少对一个测试小种表现抗病。有37份在田间成株期均表现抗病。但PI660065、PI660076、PI660079、PI660080、PI660095、PI660096和PI610750在不同年份和不同测试地点成株期表现感病。【结论】80份国外小麦种质资源中大部分对中国小麦条锈菌流行小种表现优良的抗病性。这些种质资源可作为抗源在今后抗病育种中加以利用,将丰富中国小麦抗条锈病基因的多样性。可能由于不同年份田间流行小种不同,造成一些成株抗病品系在不同年份和不同测试地点表现感病,由此推测成株抗病性可能也具有小种专化性。

小麦热激蛋白基因TaHSP70克隆及其在植物防卫和抗逆反应中的表达分析

热激蛋白是一类结构非常保守的分子伴侣类型的应激蛋白,在调控动、植物代谢和信号传导等方面发挥重要作用。本研究利用同源克隆法,筛选非亲和条锈菌小种CYR32侵染诱导的cDNA文库,分离获得1个HSP70家族基因的全长cDNA序列TaHSP70。序列分析发现,该cDNA片段包含1个2 412 bp开放阅读框,推测其编码包含691个氨基酸残基的蛋白质,属于质体间质亚族蛋白。半定量RT-PCR方法分析发现,在小麦幼苗受到低温、干旱和植物激素ABA胁迫处理后,TaHSP70表达受到抑制。利用条锈菌非亲和小种CYR32和白粉菌亲和小种混合菌系接种后以及高温胁迫条件下,TaHSP70表达量增加。说明小麦HSP70家族基因TaHSP70可能参与调控小麦抗逆和防卫反应过程。