The highly dynamic satellitomes of cultivated wheat species
Metadata
Show full item recordEditorial
Oxford University Press
Materia
Durum wheat satellite DNA satellitome
Date
2024-08-30Referencia bibliográfica
Gálvez Galván, A. & Garrido Ramos, M.A. & Prieto, P. Annals of Botany XX: 1–18, 2024. [https://doi.org/10.1093/aob/mcae132]
Sponsorship
Grant PID2019-103996RB-I00 from the MCIN/AEI/10.13039/501100011033 from Ministerio de Ciencia e Innovación; Qualifica Project QUAL21_023 IAS; Consejería de Transformación Económica, Industria, Conocimiento y Universidades/ Cofinanciación; Programa Operativo FEDER de Andalucía 2014-2020; Spanish MCIN for her PhD PRE2020-094798 grantAbstract
• Background and Aims Durum wheat, Triticum turgidum, and bread wheat, Triticum aestivum, are two allopolyploid
species of very recent origin that have been subjected to intense selection programmes during the thousands
of years they have been cultivated. In this paper, we study the durum wheat satellitome and establish a
comparative analysis with the previously published bread wheat satellitome.
• Methods We revealed the durum wheat satellitome using the satMiner protocol, which is based on consecutive
rounds of clustering of Illumina reads by RepeatExplorer2, and we estimated abundance and variation for each
identified satellite DNA (satDNA) with RepeatMasker v4.0.5. We also performed a deep satDNA family characterization
including chromosomal location by fluorescence in situ hybridization (FISH) in durum wheat and
its comparison with FISH patterns in bread wheat. BLAST was used for trailing each satDNA in the assembly
of durum wheat genome through NCBI’s Genome Data Viewer and the genome assemblies of both species were
compared. Sequence divergence and consensus turnover rate between homologous satDNA families of durum and
bread wheat were estimated using MEGA11.
• Key Results This study reveals that in an exceedingly short period, significant qualitative and quantitative
changes have occurred in the set of satDNAs of both species, with expansions/contractions of the number of
repeats and the loci per satellite, different in each species, and a high rate of sequence change for most of these
satellites, in addition to the emergence/loss of satDNAs not shared between the two species analysed. These evolutionary
changes in satDNA are common between species but what is truly remarkable and novel is that these
processes have taken place in less than the last ~8000 years separating the two species, indicating an accelerated
evolution of their satDNAs.
• Conclusions These results, together with the relationship of many of these satellites with transposable elements
and the polymorphisms they generate at the level of centromeres and subtelomeric regions of their chromosomes,
are analysed and discussed in the context of the evolutionary origin of these species and the selection pressure
exerted by humans throughout the history of their cultivation.