Segregation distortion and linkage studies in microspore-derived double haploid lines of Hordeum vulgare L.

1992 ◽  
Vol 83-83 (6-7) ◽  
pp. 919-924 ◽  
Author(s):  
M. Zivy ◽  
P. Devaux ◽  
J. Blaisonneau ◽  
R. Jean ◽  
H. Thiellement
1971 ◽  
Vol 13 (3) ◽  
pp. 489-498
Author(s):  
R. W. Matchett ◽  
H. G. Nass ◽  
D. W. Robertson

This study was initiated to determine the chromosomal location of the grandpa (gp) gene within the barley genome. The gp gene was placed on the long arm of chromosome 2 as indicated by linkage association with liguleless (li).Tests of allelism showed the gp gene to the allelic with the gp-2 gene. Seven sources of "yellow" chlorophyll mutants when crossed to grandpa plants gave albino double recessive seedlings. Three other sources of "yellow" chlorophyll mutants in the double recessive combination with grandpa exhibited yellow and white bands on the leaves. Double recessive individuals carrying the mottled (mt2) and grandpa genes were also albino. This is evidence of gene interactions between chlorophyll mutant genes.


1992 ◽  
Vol 43 (1) ◽  
pp. 67 ◽  
Author(s):  
DJ Luckett ◽  
RA Smithard

Agarose-solidified media containing maltose and glutamine were used to produce double-haploid lines, by anther culture, from Australian spring barley (Hordeum vulgare L.) genotypes. Three sets of F1 and two sets of F2 breeder's hybrids were used. Genotype differences were significant for the proportion of anthers responding, and the number of green and albino regenerants per 100 anthers plated. It was confirmed that the environmental conditions experienced by the donor plants (time of year, and field or glasshouse) had a large impact upon explant performance in culture. A minimum level of anther culture efficiency was achieved to allow a breeding program to produce all its inbred lines by this method. The procedure has the potential to save research costs, and deliver improved genotypes to the grower up to four years earlier than conventional methods.


2010 ◽  
Vol 119 (1) ◽  
pp. 36-47 ◽  
Author(s):  
Gisela Borràs-Gelonch ◽  
Gustavo A. Slafer ◽  
Ana M. Casas ◽  
Fred van Eeuwijk ◽  
Ignacio Romagosa

Author(s):  
R.H.M. Cross ◽  
C.E.J. Botha ◽  
A.K. Cowan ◽  
B.J. Hartley

Senescence is an ordered degenerative process leading to death of individual cells, organs and organisms. The detection of a conditional lethal mutant (achloroplastic) of Hordeum vulgare has enabled us to investigate ultrastructural changes occurring in leaf tissue during foliar senescence.Examination of the tonoplast structure in six and 14 day-old mutant tissue revealed a progressive degeneration and disappearance of the membrane, apparently starting by day six in the vicinity of the mitochondria associated with the degenerating proplastid (Fig. 1.) where neither of the plastid membrane leaflets is evident (arrows, Fig. 1.). At this stage there was evidence that the mitochondrial membranes were undergoing retrogressive changes, coupled with disorganization of cristae (Fig. 2.). Proplastids (P) lack definitive prolamellar bodies. The cytoplasmic matrix is largely agranular, with few endoplasmic reticulum (ER) cisternae or polyribosomal aggregates. Interestingly, large numbers of actively-budding dictysomes, associated with pinocytotic vesicles, were observed in close proximity to the plasmalemma of mesophyll cells (Fig. 3.). By day 14 however, mesophyll cells showed almost complete breakdown of subcellular organelle structure (Fig. 4.), and further evidence for the breakdown of the tonoplast. The final stage of senescence is characterized by the solubilization of the cell wall due to expression and activity of polygalacturonase and/or cellulose. The presence of dictyosomes with associated pinocytotic vesicles formed from the mature face, in close proximity to both the plasmalemma and the cell wall, would appear to support the model proposed by Christopherson for the secretion of cellulase. This pathway of synthesis is typical for secretory glycoproteins.


Author(s):  
А.В. ЖЕЛЕЗНОВ ◽  
◽  
Н.Б. ЖЕЛЕЗНОВА ◽  
Т.В. КУКОЕВА ◽  
Н.В. БУРМАКИНА ◽  
...  

Author(s):  
А.В. ДИКАРЕВ ◽  
◽  
В.Г. ДИКАРЕВ ◽  
Н.С. ДИКАРЕВА ◽  
С.А. ГЕРАСЬКИН ◽  
...  

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