cytoplasm type
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2016 ◽  
Vol 5 (1) ◽  
pp. 22-28 ◽  
Author(s):  
Jagesh Kumar Tiwari ◽  
Sapna Devi ◽  
Poonam Chandel ◽  
Nilofer Ali ◽  
Vinay Bhardwaj ◽  
...  

2014 ◽  
Vol 13 (3) ◽  
pp. 238-246 ◽  
Author(s):  
Eliana Monteverde ◽  
Guillermo A. Galván ◽  
Pablo Speranza

In Uruguay, onion (Allium cepa L.) germplasm is mainly derived from the genetic material introduced by several waves of European immigrants and subsequently multiplied by household farmers, resulting in a wealth of locally adapted populations. This study examined the genetic diversity in a collection of 27 local onion populations and two cultivars derived from them. A total of 843 onion plants were fingerprinted, and 83 inter-simple sequence repeat polymorphic bands were generated. Analysis of molecular variance showed high diversity within the populations (66% of the total variation). Some short-day populations from different geographical origins were grouped together by the unweighted pair-group method using arithmetic averages, principal coordinate analysis and cluster analysis, while the more extensively sampled long- and intermediate-day populations showed a widespread distribution, with no significant subgrouping among them. This weakly structured gene pool is probably the consequence of seed and bulb exchange between farmers and natural inter-pollination. Nevertheless, a Bayesian analysis allowed the distinction of four genetic backgrounds of alleles in the whole collection, and populations were predominately assigned to each genetic background. In addition, mitochondrial variants determining normal (N) pollen fertility or the sterile S or T types were analysed for the same set of plants using specific primers. Most accessions showed a proportion of male-sterile individuals. Cytoplasm type T was the most represented (26 out of 29 accessions), and cytoplasm type S was found in a low proportion of individuals in seven populations. Uruguayan onion germplasm maintains a low degree of genetic differentiation despite the small cultivated area and intense seed exchange, probably due in part to different market purposes based on the growing cycle.


Euphytica ◽  
2007 ◽  
Vol 162 (1) ◽  
pp. 69-80 ◽  
Author(s):  
Vivek P. Chimote ◽  
Swarup K. Chakrabarti ◽  
Debasis Pattanayak ◽  
Suman K. Pandey ◽  
Prakash S. Naik

Genetics ◽  
1985 ◽  
Vol 109 (2) ◽  
pp. 427-439
Author(s):  
M D Ross ◽  
H R Gregorius

ABSTRACT Gynodioecy is apparently frequently inherited through gene-cytoplasm interactions. General conditions for the protectedness of gene-cytoplasm polymorphisms for a biallelic model with two cytoplasm types were obtained previously, and these are applied to seven special cases of gene-cytoplasm interactions controlling gynodioecy and involving dominance. It is assumed that nuclear polymorphisms cannot be maintained in one cytoplasm type only. It is held that pure cytoplasmic inheritance of gynodioecy without nuclear interactions is unlikely, and it is shown that gynodioecy with gene-cytoplasm interactions is easier to establish than purely nuclear gynodioecy, for monogenic biallelic dominant or recessive inheritance. For three special cases, a resource-allocation model with simple assumptions always leads to conditions for protectedness of gynodioecy.


Genetics ◽  
1984 ◽  
Vol 107 (1) ◽  
pp. 165-178
Author(s):  
H R Gregorius ◽  
M D Ross

ABSTRACT General conditions for the protectedness of gene-cytoplasm polymorphisms are considered for a biallelic model with two cytoplasm types and under the assumption that nuclear polymorphisms cannot be maintained in the presence of only one cytoplasm type. Analytical results involving male fertilities, female fertilities, viabilities and selfing rates are obtained, and numerical results show spiral and cyclic behavior of population trajectories. It is shown that a maternally inherited cytoplasmic polymorphism cannot be maintained in the absence of a nuclear polymorphism, and that a gene-cytoplasm polymorphism can only be maintained if the population shows sexual asymmetry, i.e., if the ratio of male to female fertility varies among genotypes. Thus, the classical viability selection model does not allow gene-cytoplasm polymorphisms.


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