Breeding at the 2x level and sexual polyploidization

Author(s):  
S.A. Hermundstad ◽  
S.J. Peloquin
Euphytica ◽  
2007 ◽  
Vol 160 (2) ◽  
pp. 207-215 ◽  
Author(s):  
Shujun Zhou ◽  
M. S. Ramanna ◽  
Richard G. F. Visser ◽  
Jaap M. van Tuyl

Euphytica ◽  
1989 ◽  
Vol 43 (1-2) ◽  
pp. 1-6 ◽  
Author(s):  
C. A. Sala ◽  
E. L. Camadro ◽  
M. T. Salaberry ◽  
A. O. Mendiburu

2012 ◽  
pp. 107-112
Author(s):  
L. Augustin ◽  
S. Salazar ◽  
M.I. Baggio ◽  
M.F. Grando ◽  
M. Valiati ◽  
...  

Euphytica ◽  
2011 ◽  
Vol 186 (3) ◽  
pp. 731-739 ◽  
Author(s):  
Riccardo Aversano ◽  
Stefano Capomaccio ◽  
Domenico Carputo ◽  
Fabio Veronesi ◽  
Daniele Rosellini

Genome ◽  
1991 ◽  
Vol 34 (1) ◽  
pp. 28-34 ◽  
Author(s):  
Kazuo Watanabe ◽  
Stanley J. Peloquin ◽  
Masatoshi Endo

Computer simulation was undertaken to compare the genetic consequences of asexual (somatic doubling) and sexual (2n gametes) polyploidization. The coefficient of inbreeding at a locus, the number and frequency of genotypes at a locus, and the proportion of tri- and tetra-allelic genotypes were considered. The factors considered to estimate the genetic consequences were (i) mechanisms of sexual polyploidization, by first division restitution (FDR) × second division restitution (SDR), FDR × FDR, or SDR × SDR; (ii) position of the locus in relation to the centromere, which affects the gametic output in 2n gamete formation and thus the probability of single-exchange tetrads in meiosis during 2n gamete formation (p value); and (iii) allelic diversity at a locus. In comparing asexual and sexual polyploidization, regardless of the position of a locus in relation to the centromere, sexual polyploidization generally indicated less inbreeding, more genotypic diversity, and a higher proportion of tri- and tetra-allelic genotypes. When allelic diversity at a locus was increased, these characteristics were even more prominent. When only two alleles are possible at a locus, somatic doubling would not be inferior to sexual polyploidization. Overall results favored SDR × FDR and FDR × FDR as a mode and mechanisms of polyploidization. The genetic variations produced by 2n gametes could be attributed to "combining ability of 2n gametes."Key words: asexual polyploidization, sexual polyploidization, inbreeding, heterozygosity, combining ability of 2n gametes.


Genetics ◽  
2003 ◽  
Vol 163 (1) ◽  
pp. 287-294 ◽  
Author(s):  
Domenico Carputo ◽  
Luigi Frusciante ◽  
Stanley J Peloquin

Abstract Polyploidization has played a major role in the origin and evolution of polyploid species. In this article we outline the unique characteristics of 2n gametes and implications of their participation in the evolution of polyploid Solanum species. The genetic consequences of 2n gametes indicate that sexual polyploidization results in greater variability, fitness, and heterozygosity than does somatic doubling. Further, the mechanisms of 2n gamete formation and the frequency of 2n gamete-forming genes in present polyploids and their ancestral species provide additional evidence of their involvement. Equally important is the endosperm, via the endosperm balance number (EBN) incompatibility system, in complementing the role of 2n gametes. In fact, the EBN system acts as a screen for either 1n or 2n gametes, depending on the EBN and chromosome numbers of parental species. EBN in combination with 2n gametes maintains the ploidy integrity of diploid ancestral species, while providing the flexibility for either unilateral or bilateral sexual polyploidization.


1985 ◽  
Vol 27 (1) ◽  
pp. 64-68 ◽  
Author(s):  
W. A. Parrott ◽  
R. R. Smith ◽  
M. M. Smith

Twenty-four diploid red clover (Trifolium pratense L.) plants, from the cultivars 'Arlington', 'Florex', and 'Redman', and C760, a Wisconsin synthetic, were tested for 2n egg production by crossing them with tetraploid plants. Four plants were identified and selected as 2n egg producers. These plants were then crossed with a known producer of 2n pollen in an attempt to obtain tetraploid plants through bilateral sexual polyploidization. Thirteen percent of the seed obtained in one of the 2x–2x crosses were tetraploid. The female plant produced an estimated 0.14 2n eggs per 1000 flowers in the cross. In a second experiment, bilateral sexual polyploidization was attempted, using 14 plants which had not been previously tested for 2n egg production. Two of these plants produced one and two tetraploids each, representing 2n egg frequencies of 3.33 and 5.00 2n eggs per 1000 flowers, respectively. It seems likely that it will be possible to use bilateral sexual polyploidization to tetraploidize red clover germplasm in the future.Key words: tetraploid red clover, Trifolium pratense. 2n gametes.


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