Transcriptome profiling of cold hardiness related genes in peach tree (Prunus persica) shoots

2020 ◽  
pp. 649-654
Author(s):  
J. Park ◽  
D.J. Yu ◽  
S. Chea ◽  
J.H. Kwon ◽  
H.J. Lee
Genes ◽  
2020 ◽  
Vol 11 (6) ◽  
pp. 611
Author(s):  
Duk Jun Yu ◽  
Sung Hoon Jun ◽  
Junhyung Park ◽  
Jung Hyun Kwon ◽  
Hee Jae Lee

We analyzed the transcriptomes in the shoots of five-year-old ‘Soomee’ peach trees (Prunus persica) during cold acclimation (CA), from early CA (end of October) to late CA (middle of January), and deacclimation (DA), from late CA to late DA (middle of March), to identify the genes involved in cold hardiness. Cold hardiness of the shoots increased from early to late CA, but decreased from late CA to late DA, as indicated by decreased and increased the median lethal temperature (LT50), respectively. Transcriptome analysis identified 17,208 assembled transcripts during all three stages. In total, 1891 and 3008 transcripts were differentially expressed with a |fold change| > 2 (p < 0.05) between early and late CA, and between late CA and late DA, respectively. Among them, 1522 and 2830, respectively, were functionally annotated with gene ontology (GO) terms having a greater proportion of differentially expressed genes (DEGs) associated with molecular function than biological process or cellular component categories. The biochemical pathways best represented both periods from early to late CA and from late CA to late DA were ‘metabolic pathway’ and ‘biosynthesis of secondary metabolites’. We validated these transcriptomic results by performing reverse transcription quantitative polymerase chain reaction on the selected DEGs showing significant fold changes. The relative expressions of the selected DEGs were closely related to the LT50 values of the peach tree shoots: ‘Soomee’ shoots exhibited higher relative expressions of the selected DEGs than shoots of the less cold-hardy ‘Odoroki’ peach trees. Irrespective of the cultivar, the relative expressions of the DEGs that were up- and then down-regulated during CA, from early to late CA, and DA, from late CA to late DA, were more closely correlated with cold hardiness than those of the DEGs that were down- and then up-regulated. Therefore, our results suggest that the significantly up- and then down-regulated DEGs are associated with cold hardiness in peach tree shoots. These DEGs, including early light-induced protein 1, chloroplastic, 14-kDa proline-rich protein DC2.15, glutamate dehydrogenase 2, and triacylglycerol lipase 2, could be candidate genes to determine cold hardiness.


HortScience ◽  
2001 ◽  
Vol 36 (1) ◽  
pp. 101-103 ◽  
Author(s):  
T.G. Beckman ◽  
P.L. Pusey

Armillaria root rot is the second leading cause of peach tree mortality (after peach tree short life) in the southeastern United States. Currently, there are no commercially available rootstocks for peach with proven resistance to this pathogen in the United States. Since 1983, we have been screening rootstock candidates for resistance to Armillaria utilizing naturally infected field sites. Inoculation of peach [Prunus persica (L.) Batsch], plum (P. cerasifera J.F. Ehrh., P. munsoniana F.W. Wight & Hedr., P. salicina Lindl. or P. angustifolia Marsh.) × peach and plum × plum hybrid rootstocks with infected plant tissue (such as acorns, Quercus sp.) prior to planting has provided a significantly increased infection and mortality of candidate rootstock lines in comparison with sole reliance on natural inoculum on an infested site.


HortScience ◽  
1998 ◽  
Vol 33 (6) ◽  
pp. 1062-1065 ◽  
Author(s):  
T.G. Beckman ◽  
W.R. Okie ◽  
A.P. Nyczepir ◽  
P.L. Pusey ◽  
C.C. Reilly

Nearly 5000 seedling trees representing more than 100 peach [Prunus persica (L.) Batsch.] and plum (Prunus spp.) lines were planted at a 4 × 0.6-m spacing in Jan. 1983, on a site with a known history of peach tree short life (PTSL) and Armillaria root rot (ARR). Trees were arranged in a randomized complete-block with eight replicates of six trees each. Beginning in Spring 1984 and each year thereafter the cause of tree death was determined. At the end of 9 years, 50% of the trees had succumbed to PTSL and 35% had been killed by ARR apparently caused by Armillaria tabescens. Analysis of the data for trees killed by ARR showed a wide range in mortality, some peach lines appeared significantly more tolerant to ARR than others. Plum lines derived from native North American species also appeared to be a potential source of improved tolerance. We did not establish whether ARR tolerance is affected by PTSL.


2019 ◽  
Vol 180 (3) ◽  
pp. 212-220 ◽  
Author(s):  
Laura Victorio Puche ◽  
Maria Luisa Somoza ◽  
José Damián López-Sánchez ◽  
María Garrido-Arandia ◽  
Araceli Díaz-Perales ◽  
...  

2017 ◽  
Vol 219 ◽  
pp. 45-52 ◽  
Author(s):  
Duk Jun Yu ◽  
Ju Young Hwang ◽  
Sun Woo Chung ◽  
Hee Duk Oh ◽  
Seok Kyu Yun ◽  
...  

2017 ◽  
Vol 39 (2) ◽  
pp. 218-228 ◽  
Author(s):  
Rana Samara ◽  
David M. Hunter ◽  
Lorne W. Stobbs ◽  
Neva Greig ◽  
D. Thomas Lowery ◽  
...  

2009 ◽  
Vol 134 (2) ◽  
pp. 236-243 ◽  
Author(s):  
Dongyan Hu ◽  
Ralph Scorza

Since the first report of the ‘A72’ semidwarf peach [Prunus persica (L.) Batsch] tree in 1975, no new information has become available on this genotype. We evaluated the growth habit and verified the inheritance of ‘A72’ in a population of 220 progeny derived from self-pollination. Detailed tree and branch measurements revealed a unique forked-branch (FBR) character of the ‘A72’ (Nn) phenotype. The progeny segregated into 1 NN:2 Nn:1 nn. NN trees were indistinguishable from standard peach trees, Nn were FBR, and nn were dwarf. Hybrids between ‘A72’ and columnar (brbr) peach trees confirmed that FBR is inherited as a monogenic trait that appears to express incomplete dominance. ‘A72’ (Nn) trees were later blooming than sibling NN trees. The relationship (linkage or pleiotropy) between the growth habit of ‘A72’ and late bloom is not known. The structure of ‘A72’ trees presents new opportunities to breeder/geneticists, physiologists, and horticulturists to further explore the plasticity of peach tree growth and architecture that can be achieved through breeding. Applications of the ‘A72’ growth habit for commercial fruit production and as an ornamental, particularly in the dwarf form (nn) and in combination with the columnar tree (brbr) form, present opportunities that await exploration.


HortScience ◽  
1997 ◽  
Vol 32 (5) ◽  
pp. 840-843 ◽  
Author(s):  
S.K. Kang ◽  
H. Motosugi ◽  
K. Yonemori ◽  
A. Sugiura

Microcomputer-based thermal analysis (TA) was conducted on dormant mixed buds of Japanese persimmon (`Hiratanenashi'). The exotherms of buds were detected by thermoelectric modules. Flower buds of peach (Prunus persica Batsch cv. Shimizuhakuto) were also analyzed. When TA was used on a whole excised bud, including bud scales, the persimmon buds had only one exotherm at –14.3 °C, while the peach buds had high and low exotherms at –8.4 °C and –14.1 °C, respectively. However, when the exotherm was measured for the primordium, with the bud scales and transitional leaves removed, each primordium showed only one exotherm at –20.7 °C in persimmon and –11 °C in peach. Determination of killing temperature by visual observation, electrolyte leakage method, and triphenyltetrazolium chloride test revealed that the primordium of the persimmon bud was killed at about –14 °C as the excised whole bud or as the whole bud attached to the branch segment. Using the same method, the naked primordium was killed between –22 °C and –25 °C as the primordium was cooled. The peach primordium was killed at –14 °C when examined as a whole bud and at –11 °C as a naked primordium. Furthermore, the exotherm temperatures of persimmon buds and stem segments were measured at appropriate intervals during the two winter seasons 1993–95. Exotherm temperatures of persimmon buds were always higher than the low-temperature exotherm (LTE) temperatures of the stem segments and lower than the high-temperature exotherm (HTE) temperatures of the stem segments. LT50 of persimmon buds almost coincided with the exotherm temperatures of buds. A postulated role of bud scales in supercooling is discussed.


HortScience ◽  
1997 ◽  
Vol 32 (3) ◽  
pp. 514B-514
Author(s):  
Michael Wisniewski ◽  
Tim Artlip ◽  
Carole Bassett ◽  
Ann Callahan

Cold acclimation in temperate, woody plants involves distinct changes in gene activity and protein expression. We have been identifying proteins and genes that are associated with seasonal changes in cold hardiness. Seasonal changes in a 60-kDa dehydrin and its corresponding transcript have been identified, as well as seasonal changes in 16- and 19-kDa storage proteins. Further screening of a cDNA library, constructed from cold-acclimated bark tissues collected in December, identified a 700–800-bp clone that was seasonally expressed in Northern blots. The transcript began to accumulate in October, reached a peak in November–December, and then began to decline. By April, the transcript was no longer present in bark tissues. The transcript size indicates that this gene my be related to either the 16- or 19-kDa storage proteins previously identified; however, an amino acid sequence of the protein for comparison has not yet been obtained. Interestingly, the transcript is also expressed during the early stages of peach fruit development. A similar pattern between seasonal expression and fruit development has been observed for a peach dehydrin transcript. Analysis of a partial sequence of the clone has indicated a similarity to genes encoding proteinase inhibitors and thionins (a class of biocidal proteins). More definitive characterization of the gene and identification of its corresponding protein are in progress.


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