plant hybridization
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2021 ◽  
pp. 1-17
Author(s):  
M. Arockia Dasan ◽  
E. Bementa ◽  
Florentin Smarandache ◽  
X. Tubax

2020 ◽  
Vol 34 (2) ◽  
pp. 229-242 ◽  
Author(s):  
Luiz Rezende ◽  
João Suzigan ◽  
Felipe W. Amorim ◽  
Ana Paula Moraes

2020 ◽  
Vol 71 (1) ◽  
pp. 517-546 ◽  
Author(s):  
Friederike Hater ◽  
Thomas Nakel ◽  
Rita Groß-Hardt

Fertilization of flowering plants requires the organization of complex tasks, many of which become integrated by the female gametophyte (FG). The FG is a few-celled haploid structure that orchestrates division of labor to coordinate successful interaction with the sperm cells and their transport vehicle, the pollen tube. As reproductive outcome is directly coupled to evolutionary success, the underlying mechanisms are under robust molecular control, including integrity check and repair mechanisms. Here, we review progress on understanding the development and function of the FG, starting with the functional megaspore, which represents the haploid founder cell of the FG. We highlight recent achievements that have greatly advanced our understanding of pollen tube attraction strategies and the mechanisms that regulate plant hybridization and gamete fusion. In addition, we discuss novel insights into plant polyploidization strategies that expand current concepts on the evolution of flowering plants.


2019 ◽  
Author(s):  
Kevin A. Bird ◽  
Chad Niederhuth ◽  
Shujun Ou ◽  
Malia Gehan ◽  
J. Chris Pires ◽  
...  

AbstractInterspecific hybridization and allopolyploidization merges evolutionarily distinct parental genomes (subgenomes) into a single nucleus. A frequent observation is that one subgenome is “dominant” over the other subgenome, having a greater number of reatined duplicate genes and being more highly expressed. Which subgenome becomes dominantly expressed in allopolyploids remains poorly understood. Here we “replayed the evolutionary tape” with six isogenic resynthesized Brassica napus (rapeseed) allopolyploid lines and investigated subgenome dominance patterns over the first ten generations. We found that the same subgenome was consistently more dominantly expressed in all lines and generations. Furthermore, DNA methylation differences between subgenomes mirrored the observed gene expression bias towards the Brassica oleracea derived ‘C’ subgenome in all lines and generations. These differences in gene expression and methylation were also found when comparing the progenitor genomes, suggesting subgenome dominance is related to inherited parental genome differences rather than a byproduct of allopolyploidization. Gene network analyses indicated an enrichment for network interactions and several biological functions for ‘C’ subgenome biased pairs, but no enrichment was observed for ‘A’ subgenome biased pairs. These findings demonstrate that “replaying the evolutionary tape” in allopolyploids results in repeatable and predictable subgenome expression dominance patterns based on preexisting genetic differences among the parental species. These findings have major implications regarding the genotypic and phenotypic diversity observed following plant hybridization in both ecological and agricultural contexts.


Author(s):  
Immaculate Mueni Mwangangi ◽  
Joshua Kiilu Muli ◽  
Johnstone Omukhulu Neondo

For ages, plant breeders have relied on the genetic variability that results from sexually crossing plants within the same species. However, the variability that exists within species populations is inadequate, hence the need to exploit desirable traits of interest in distantly related or even unrelated plants through hybridization techniques. Hybridization can be categorized into two; sexual and somatic. Sexual hybridization, also referred to as wide or distant hybridization involves combining two genomes from different parental taxa through pollination, either naturally or by induction. Somatic hybridization involves the fusion of somatic cells instead of gametes, which highly depends on the ability to obtain viable protoplasts and eventually differentiate them to whole plants in vitro. The impacts of hybrids can either be positive or negative. Among the positive attributes of hybrids that have been exploited is heterosis, which results either from dominance, over-dominance or epistasis. Negative ones include sterility, arrested growth of the pollen tube and embryo abortion. To overcome these problems, chromosome doubling, the use of hormones such as 2, 4-Dichlorophenoxyacetic acid (2, 4-D) and embryo rescue have been employed to overcome sterility, arrested growth of pollen tubes and embryo abortion respectively. After the development of hybrids, different hybrid identification techniques have been used to test them such as the use of molecular and morphological markers, cytogenetic analysis and fluorescent in situ hybridization. The use of hybridization techniques in plant improvement remains a vital tool to cross species barriers and utilization of important attributes in unrelated crop plants which could not have been achieved through conventional techniques of plant breeding.


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