1996 ◽  
Vol 121 (6) ◽  
pp. 1028-1031 ◽  
Author(s):  
Mark J. Bassett

The inheritance of hilum ring color in common bean (Phaseolus vulgaris L.) was investigated using various genetic tester stocks developed by backcrossing recessive alleles into a recurrent parent stock 5-593 with seedcoat genotype P [C r] D J G B V Rk, viz., mar BC2 5-593, mar BC3 5-593, mar v BC2 5-593, mar d BC2 5-593, and mar d BC3 5-593. The current hypothesis is that the margo character is controlled by mar and hilum ring color is controlled by d but expresses only with mar. The V locus controls flower and seedcoat color. The allelism test crosses `Citroen' (P C d j g b vlae) × mar BC3 5-593 and `Citroen' × mar d BC3 5-593 demonstrated that mar is allelic with j and that the putative d in mar d BC3 5-593 is allelic with the d in `Citroen'. Thus, the former genetic tester stocks mar BC3 5-593 and mar d BC3 5-593 are reclassified as j BC3 5-593 and d j BC3 5-593, respectively, because mar is a synonym for j. Similarly, the former genetic tester stock mar v BC2 5-593 is reclassified as j v BC2 5-593. The interaction of j with d expresses as loss of color in the hilum ring. The development of the white-seeded genetic tester stock P cu d j BC3 5-593 was described in detail, where the all-recessive tester `Prakken 75' was used as the source of the recessive alleles. The previously reported work showing that the partly colored seedcoat gene t interacts with mar to control seedcoat pattern is now interpreted to mean that the joker (J) locus interacts with t to produce partly colored seedcoat patterns. The genetic loci D and V were found to segregate independently. The common gene for dull seedcoats (asper, asp) is discussed and contrasted with j.


2009 ◽  
Vol 89 (5) ◽  
pp. 845-850 ◽  
Author(s):  
Z Wang ◽  
D Xu ◽  
J Ji ◽  
J Wang ◽  
M Wang ◽  
...  

Trigrain wheat normally produces up to three gynoecia in a single floret and forms three close-set grains. The gene conferring the multi grain phenotype was earlier designated Mg, the multiple gynoecia gene. Different genetic patterns controlling this trait have been reported. In the present work we studied the inheritance of the three grains trait and identified simple sequence repeats (SSR) markers linked to the Mg gene. Segregation analysis in the cross IGDB-TW (trigrain wheat)/Chinese Spring confirmed that a single dominant gene controlled the three grains trait. An allelism test showed that the same gene controlled the trigrain trait in line Trigrain-Yin 1. A total of 339 microsatellite markers were tested for polymorphism by bulked segregation analysis (BSA) in an F2 population. Six microsatellite markers, Xcfd233, Xgdm6, Xgdm87, Xgwm311, Xgwm349 and Xgwm539, on chromosome 2DL, were linked to Mg. Using the CS 2D deletion lines, Mg gene was localized to the distal region of chromosome 2DL. The microsatellite markers identified in this study have the potential for further mapping and map-based cloning of the gene.Key words: Simple sequence repeats, physical mapping, trigrain wheat


2009 ◽  
Vol 37 (1) ◽  
pp. 37-43 ◽  
Author(s):  
E. Khlestkina ◽  
E. Salina ◽  
T. Pshenichnikova ◽  
M. Röder ◽  
A. Börner

1998 ◽  
Vol 48 (1) ◽  
pp. 93-94
Author(s):  
Chikako Kiribuchi- Otobe ◽  
Takeshi Yasui ◽  
Takashi Yanagisawa ◽  
Hisashi Yoshida

2011 ◽  
Vol 47 (4) ◽  
pp. 483-488
Author(s):  
A. V. Smiryaev

Euphytica ◽  
2007 ◽  
Vol 157 (1-2) ◽  
pp. 267-279 ◽  
Author(s):  
K. Himabindu ◽  
R. M. Sundaram ◽  
C. N. Neeraja ◽  
B. Mishra ◽  
J. S. Bentur

2020 ◽  
Vol 47 (3) ◽  
pp. 135-138
Author(s):  
W. D. Branch ◽  
A. M. Perera ◽  
K. Narayanaswamy

ABSTRACT Crosses were made between High-O/L x High-O/L and between Very High-O/L x Very High-O/L peanut genotypes. The High-O/L parental genotypes were F435-OL-2 and ‘Flavor Runner 458’ and ranged between 20 and 40:1 oleic (O) to linoleic (L) fatty acid methyl ester ratio. The Very High-O/L parental cultivars were ‘Georgia Hi-O/L' and ‘Georgia-11J' and consistently had O/L ratios ≥40:1 over four years at the Tifton, Georgia location when grown under maximum-input production practices with irrigation. F1 plants from the High-O/L x High-O/L cross combination had an average O/L ratio of 32.5:1; whereas, the F1 plants from the Very High-O/L x Very High-O/L crosses had an average O/L ratio of 50:1. Average O/L ratios of both F2 and F3 generation progeny also had similar O/L ratios within High-O/L x High-O/L and Very High-O/L x Very High-O/L crosses. The results from these test crosses suggest that there are at least two different high-oleic genotypes possibly associated with either multiple alleles or modifier genes.


1995 ◽  
Vol 90 (7-8) ◽  
pp. 1188-1197 ◽  
Author(s):  
B.-S. Seo ◽  
P. A. Peterson

2000 ◽  
Vol 125 (3) ◽  
pp. 340-343 ◽  
Author(s):  
Mark J. Bassett ◽  
Kirk Hartel ◽  
Phil McClean

Inheritance of Anasazi pattern of partly colored seedcoats in common bean (Phaseolus vulgaris L.) was studied in a genetic stock t ana B V Anasazi BC3 5-593, whose Anasazi pattern is derived from Plant Introduction (PI) 451802. Line 5-593 is a determinate, Florida dry bean breeding line (with small black seeds) used as the recurrent parent in the development of many genetic stocks. The F2 from the cross t ana B V Anasazi BC3 5-593 × t z virgarcus BC3 5-593 segregated for two nonparental phenotypic classes and was consistent with the hypothesis that a single recessive gene, with tentative symbol ana, produces the Anasazi pattern with t Z ana and a new partly colored pattern Anabip with t z ana. Thus, the Anasazi factor is not an allele at the Z locus. Analysis of 57 random F3 progenies from the cross t ana B V Anasazi BC3 5-593 × t z virgarcus BC3 5-593 supported a genetic model where: 1) with t Z the Anasazi phenotype is controlled by a single recessive gene ana, i.e., genotype t Z ana, 2) the Anabip phenotype has the genotype t z ana, and 3) t Z/z ana produces a restricted Anasazi pattern. The allelism test cross t z ana Anabip BC3 5-593 × t z lers white BC3 5-593 produced complementation in the F2, demonstrating nonallelism of Ana (actually Bip) with the L locus. The allelism test cross t z ana Anabip BC3 5-593 × t z bip bipunctata BC3 5-593 failed to show complementation in F1 and F2, demonstrating allelism of Ana with the Bip locus. Using bulk segregant analysis, molecular markers linked in coupling to the Ana (OM9200, 5.4 cM) and Bip (OJ17700, 6.0 cM) genes were discovered. Allelism was also suggested by the result that the same linkage distance and recombination pattern were observed when the Ana marker was used to score the bipunctata population. We propose the gene symbol bipana for the recessive allele at the Bip locus that produces Anasazi pattern with genotype t Z bipana and the Anabip pattern with genotype t z bipana. Although bipana and bip are both recessive to Bip, their interactions with the Z locus are extraordinarily different. The pattern restrictive power of bipana expresses partly colored pattern with t Z, whereas bip requires t z to express partly colored pattern.


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