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'''Astrids and eurosids share a paleohexaploidy'''
'''Astrids and eurosids share a paleohexaploidy'''
[[File:tomato-grape-synteny.png]]
[[File:grape-tomato-synteny.png]]
 
The image above shows a syntenic alignment between genomic regions of grape and tomato.  Nearly every gene in grape has a syntenic match to tomato (the tomato genomic region is not annotated).  This near-perfect one-to-one mapping of gene between fairly distantly related plant genomes (one from each of two major groups of eudicots -- eurosids and astrids) is the expected pattern if neither genome has undergone one or more independent whole genome duplication (WGD) events.  In plants, following WGD, each duplicated genomic region undergoes diploidization, which reduces the total gene content of the genome to one which is more similar to the pre-duplicated ancestor genome.  This process of gene loss is known as fractionation and results in distributing ancestral gene content over all genomic duplicates.  If such a process were at work, we would not expect to see the near-perfect one-to-one mapping of gene content.  Results can be regenerated and analysis resumed using http://tinyurl.com/qjpcvv.

Revision as of 04:55, 13 May 2009

Astrids and eurosids share a paleohexaploidy

The image above shows a syntenic alignment between genomic regions of grape and tomato. Nearly every gene in grape has a syntenic match to tomato (the tomato genomic region is not annotated). This near-perfect one-to-one mapping of gene between fairly distantly related plant genomes (one from each of two major groups of eudicots -- eurosids and astrids) is the expected pattern if neither genome has undergone one or more independent whole genome duplication (WGD) events. In plants, following WGD, each duplicated genomic region undergoes diploidization, which reduces the total gene content of the genome to one which is more similar to the pre-duplicated ancestor genome. This process of gene loss is known as fractionation and results in distributing ancestral gene content over all genomic duplicates. If such a process were at work, we would not expect to see the near-perfect one-to-one mapping of gene content. Results can be regenerated and analysis resumed using http://tinyurl.com/qjpcvv.