The polymorphism of ACS1 and ACO1 genes in some Malus species

2019 ◽  
pp. 13-18
Author(s):  
S. Marić ◽  
S. Radičević ◽  
N. Milošević ◽  
M. Lukić ◽  
M. Đorđević
Keyword(s):  
2014 ◽  
Vol 61 (5) ◽  
pp. 943-964 ◽  
Author(s):  
Monika Höfer ◽  
Mohamed Ali Mohamed Saad Eldin Ali ◽  
Jörg Sellmann ◽  
Andreas Peil
Keyword(s):  

Genome ◽  
2009 ◽  
Vol 52 (2) ◽  
pp. 148-155 ◽  
Author(s):  
Schuyler S. Korban ◽  
Wannasiri Wannarat ◽  
Charlotte M. Rayburn ◽  
Tatiana C. Tatum ◽  
A. Lane Rayburn

The genus Malus has anywhere between 25 and 33 species along with several subspecies. Malus species as well as clones within the same species have varying ploidy levels, as these are more than likely collected from different trees and (or) from different locations. In recent years, large numbers of Malus germplasm accessions have been collected and maintained at the United States National Germplasm Clonal Repository; however, genome sizes of this material have not yet been determined. In this study, leaf tissues from young grafted trees of 100 Malus species and hybrids growing in a nursery at the University of Illinois were collected and immediately used for extracting nuclei. Leaf tissues from apple and maize line W-22, used as an internal standard, were co-chopped and prepared for flow cytometric analysis. Apple nuclei were stained with propidium iodide, an intercalating dye, and a minimum of 8000 nuclei per sample were analyzed. Mean fluorescence of apple nuclei was then determined. A total of four replications per sample was used. Among 100 Malus accessions analyzed, one tetraploid, three triploid, and 96 diploid genotypes were identified. Significant differences in genome size were identified among the three ploidy types observed and also within diploid genotypes. The 2C mean value for tetraploids was 3.13 pg and ranged from 2.27 to 2.41 pg for triploids, whereas 2C values for diploids ranged between 1.44 and 1.72 pg. In addition, leaf impressions of young, fully expanded leaves were collected from young trees of 10 selected genotypes based on their ploidy and flow cytometric analysis and used to measure the nucleotypic parameter stomatal length. Ten stomata were measured per slide, three slides were analyzed per leaf, and three leaves were analyzed per accession. Overall, mean length of stomata ranged between 19.47 μm (diploid) and 27.6 μm (tetraploid), indicating that stomatal length in a tetraploid Malus genotype was 1.4-fold higher than that of a diploid genotype. A positive correlation between genome size and the nucleotypic parameter stomatal length was observed.


2011 ◽  
Vol 30 (2) ◽  
pp. 453-461 ◽  
Author(s):  
Tianzhong Li ◽  
Shenshan Long ◽  
Maofu Li ◽  
Songling Bai ◽  
Wen Zhang
Keyword(s):  

2002 ◽  
pp. 369-372 ◽  
Author(s):  
H.S. Aldwinckle ◽  
H.L. Gustafson ◽  
P.L. Forsline ◽  
M.V. Bhaskara Reddy

2010 ◽  
Vol 2010 ◽  
pp. 1-8 ◽  
Author(s):  
Monika Höfer ◽  
Armin Meister

The nuclear DNA content for 256 different accessions belonging to 26 primary Malus species and 20 species hybrids was estimated by flow cytometry using propidium iodide. Diploids ranged from 1.245 (M. tschonoskii) to 1.653  pg per 2C nucleus (M. florentina). As our study covered complete phylogenetic and geographic representation, preliminary conclusions between nuclear DNA content and geographical and taxonomic features could be drawn. The data indicated that species found far from the centre of origin in Asia clustered into separate sections and series and possessed higher DNA content. These are M. trilobata and M. florentina the only two species existing in South-East Europe on one hand; M. ioensis and 3x and 4x species M. heterophylla, M. platycarpa, M. glaucescens, M. angustifolia, M. lancifolia and M. coronaria—in East and Central North America on the other hand. A significantly decreased 1Cx DNA content was observed with the increase in ploidy for six species.


1991 ◽  
Vol 116 (1) ◽  
pp. 100-106 ◽  
Author(s):  
Roberto Hauagge ◽  
James N. Cummins

The chilling requirements (CR) to break bud dormancy in a broad range of apple cultivars (Malus ×domestica Borkh.) and related Malus spp. were assessed by periodic sampling and forcing of field-grown shoots as a function of chill unit (CU) accumulation and/or by the total growing degree hours (GDH) accumulated from leaf fall until the time of budbreak under a simulated subtropical winter. The mean number of CU required to break dormancy of field overwintered shoots varied between 218 ± 113 for `Anna' and 1516 ± 113 for `Wright #1'. However, most genotypes had CR between 800 and 1200 CU. Much wider variation for the length of bud dormancy was observed in plants growing under simulated subtropic winter conditions. Genotypes that had shown the lowest CR values under Geneva, N.Y., winters generally had the highest year-to-year variation in CR estimates. Cultivar bud CR values obtained under cold winters are related to field-observed CR estimates in a subtropical environment, but absolute values may differ markedly. Furthermore, several genotypes that show reasonable adaptation to the subtropics have similar or higher CR than apple cultivars with standard CR under Geneva conditions. In addition, enough CU accumulated under the simulated subtropic winters to break dormancy of standard apple cultivars. However, complete dormancy removal was observed only in cultivars well-adapted to a subtropical environment. This result indicates that in addition to CU accumulation, there are important interactions among cultivars and environmental factors that are responsible for terminating bud dormancy. Several cultivars and wild species have shown resistance to delayed foliation. Among the species, M. brevipes, M. rockii, M. spectabilis, and M. turesii are more tolerant than M. baccata and its hybrids, which are recognized for their adaptation to the subtropic environment.


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