Phylogeny and Molecular Evolution of miR820 and miR396 microRNA Families in Oryza AA Genomes
The phylogeny and evolution of the microRNA families, miR820 and miR396 , was analysed across the AA genomes of the Oryza species, the close relatives of domesticated rice. A highly dynamic evolution of the miR820 family was revealed. The number of copies of MIR820 genes, their chromosomal location...
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Veröffentlicht in: | Tropical plant biology 2018-06, Vol.11 (1-2), p.1-16 |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The phylogeny and evolution of the microRNA families, miR820 and miR396
,
was analysed across the AA genomes of the
Oryza
species, the close relatives of domesticated rice. A highly dynamic evolution of the miR820 family was revealed. The number of copies of
MIR820
genes, their chromosomal location and the mature microRNA sequence varied greatly with a total of 16 novel miR820 variants being identified. The phylogeny of pre-
MIR820
sequences revealed that
MIR820
genes of recently evolved
Oryza
AA genomes may have derived from sequence divergence of one or a few ancestral genes found in wild Australian perennial rice populations, Taxon B (jpn2)-
MIR820
genes. Genomic scale duplication played an important role in the evolution of some of the miR396 family genes in AA genome
Oryza
species. miR396 family contained a
MIR396
gene cluster (
MIR396a
and
MIR396c
) which was conserved across the cereal genomes. Nucleotide diversity analysis at these two
MIR396
loci revealed that domesticated rice has retained less than 10% of the total diversity present in wild species. In contrast, the nucleotide sequence of four
MIR396
loci remained almost conserved across domesticated and wild rices, indicating that they were under extreme functional constraint and may be involved in regulating some fundamental processes which are important both for wild and domesticated rices. Expression analysis demonstrated that miR820 variants were expressed in
O. glaberrima O. barthi
and
O. longistaminata
genome. These findings pose new challenges to explain the possible role of miR820 variants identified. |
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ISSN: | 1935-9756 1935-9764 |
DOI: | 10.1007/s12042-017-9197-4 |