Satellite DNA in Paphiopedilum subgenus Parvisepalum as revealed by high-throughput sequencing and fluorescent in situ hybridization

Background: Satellite DNA is a rapidly diverging, largely repetitive DNA component of many eukaryotic genomes. Here we analyse the evolutionary dynamics of a satellite DNA repeat in the genomes of a group of Asian subtropical lady slipper orchids (Paphiopedilum subgenus Parvisepalum and representati...

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Main Authors: Lee, Yung-I, Yap, Jing Wei, Ramlee, Shairul Izan, Leitch, Ilia J., Fay, Michael F., Lee, Yi-Ching, Hidalgo, Oriane, Dodsworth, Steven, Smulders, Marinus J. M., Gravendeel, Barbara, Leitch, Andrew R.
Format: Article
Language:English
Published: BioMed Central 2018
Online Access:http://psasir.upm.edu.my/id/eprint/73825/1/FISH.pdf
http://psasir.upm.edu.my/id/eprint/73825/
https://pubmed.ncbi.nlm.nih.gov/30068293/
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Institution: Universiti Putra Malaysia
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spelling my.upm.eprints.738252021-07-15T23:35:28Z http://psasir.upm.edu.my/id/eprint/73825/ Satellite DNA in Paphiopedilum subgenus Parvisepalum as revealed by high-throughput sequencing and fluorescent in situ hybridization Lee, Yung-I Yap, Jing Wei Ramlee, Shairul Izan Leitch, Ilia J. Fay, Michael F. Lee, Yi-Ching Hidalgo, Oriane Dodsworth, Steven Smulders, Marinus J. M. Gravendeel, Barbara Leitch, Andrew R. Background: Satellite DNA is a rapidly diverging, largely repetitive DNA component of many eukaryotic genomes. Here we analyse the evolutionary dynamics of a satellite DNA repeat in the genomes of a group of Asian subtropical lady slipper orchids (Paphiopedilum subgenus Parvisepalum and representative species in the other subgenera/sections across the genus). A new satellite repeat in Paphiopedilum subgenus Parvisepalum, SatA, was identified and characterized using the RepeatExplorer pipeline in HiSeq Illumina reads from P. armeniacum (2n = 26). Reconstructed monomers were used to design a satellite-specific fluorescent in situ hybridization (FISH) probe. The data were also analysed within a phylogenetic framework built using the internal transcribed spacer (ITS) sequences of 45S nuclear ribosomal DNA. Results: SatA comprises c. 14.5% of the P. armeniacum genome and is specific to subgenus Parvisepalum. It is composed of four primary monomers that range from 230 to 359 bp and contains multiple inverted repeat regions with hairpinloop motifs. A new karyotype of P. vietnamense (2n = 28) is presented and shows that the chromosome number in subgenus Parvisepalum is not conserved at 2n = 26, as previously reported. The physical locations of SatA sequences were visualised on the chromosomes of all seven Paphiopedilum species of subgenus Parvisepalum (2n = 26–28), together with the 5S and 45S rDNA loci using FISH. The SatA repeats were predominantly localisedin the centromeric, peri-centromeric and sub-telocentric chromosome regions, but the exact distribution pattern was species-specific. Conclusions: We conclude that the newly discovered, highly abundant and rapidly evolving satellite sequence SatA is specific to Paphiopedilum subgenus Parvisepalum. SatA and rDNA chromosomal distributions are characteristic of species, and comparisons between species reveal that the distribution patterns generate a strong phylogenetic signal. We also conclude that the ancestral chromosome number of subgenus Parvisepalum and indeed of all Paphiopedilum could be either 2n = 26 or 28, if P. vietnamense is sister to all species in the subgenus as suggested by the ITS data. BioMed Central 2018 Article PeerReviewed text en http://psasir.upm.edu.my/id/eprint/73825/1/FISH.pdf Lee, Yung-I and Yap, Jing Wei and Ramlee, Shairul Izan and Leitch, Ilia J. and Fay, Michael F. and Lee, Yi-Ching and Hidalgo, Oriane and Dodsworth, Steven and Smulders, Marinus J. M. and Gravendeel, Barbara and Leitch, Andrew R. (2018) Satellite DNA in Paphiopedilum subgenus Parvisepalum as revealed by high-throughput sequencing and fluorescent in situ hybridization. BMC Genomics, 19 (1). pp. 1-14. ISSN 1471-2164 https://pubmed.ncbi.nlm.nih.gov/30068293/ 10.1186/s12864-018-4956-7
institution Universiti Putra Malaysia
building UPM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Putra Malaysia
content_source UPM Institutional Repository
url_provider http://psasir.upm.edu.my/
language English
description Background: Satellite DNA is a rapidly diverging, largely repetitive DNA component of many eukaryotic genomes. Here we analyse the evolutionary dynamics of a satellite DNA repeat in the genomes of a group of Asian subtropical lady slipper orchids (Paphiopedilum subgenus Parvisepalum and representative species in the other subgenera/sections across the genus). A new satellite repeat in Paphiopedilum subgenus Parvisepalum, SatA, was identified and characterized using the RepeatExplorer pipeline in HiSeq Illumina reads from P. armeniacum (2n = 26). Reconstructed monomers were used to design a satellite-specific fluorescent in situ hybridization (FISH) probe. The data were also analysed within a phylogenetic framework built using the internal transcribed spacer (ITS) sequences of 45S nuclear ribosomal DNA. Results: SatA comprises c. 14.5% of the P. armeniacum genome and is specific to subgenus Parvisepalum. It is composed of four primary monomers that range from 230 to 359 bp and contains multiple inverted repeat regions with hairpinloop motifs. A new karyotype of P. vietnamense (2n = 28) is presented and shows that the chromosome number in subgenus Parvisepalum is not conserved at 2n = 26, as previously reported. The physical locations of SatA sequences were visualised on the chromosomes of all seven Paphiopedilum species of subgenus Parvisepalum (2n = 26–28), together with the 5S and 45S rDNA loci using FISH. The SatA repeats were predominantly localisedin the centromeric, peri-centromeric and sub-telocentric chromosome regions, but the exact distribution pattern was species-specific. Conclusions: We conclude that the newly discovered, highly abundant and rapidly evolving satellite sequence SatA is specific to Paphiopedilum subgenus Parvisepalum. SatA and rDNA chromosomal distributions are characteristic of species, and comparisons between species reveal that the distribution patterns generate a strong phylogenetic signal. We also conclude that the ancestral chromosome number of subgenus Parvisepalum and indeed of all Paphiopedilum could be either 2n = 26 or 28, if P. vietnamense is sister to all species in the subgenus as suggested by the ITS data.
format Article
author Lee, Yung-I
Yap, Jing Wei
Ramlee, Shairul Izan
Leitch, Ilia J.
Fay, Michael F.
Lee, Yi-Ching
Hidalgo, Oriane
Dodsworth, Steven
Smulders, Marinus J. M.
Gravendeel, Barbara
Leitch, Andrew R.
spellingShingle Lee, Yung-I
Yap, Jing Wei
Ramlee, Shairul Izan
Leitch, Ilia J.
Fay, Michael F.
Lee, Yi-Ching
Hidalgo, Oriane
Dodsworth, Steven
Smulders, Marinus J. M.
Gravendeel, Barbara
Leitch, Andrew R.
Satellite DNA in Paphiopedilum subgenus Parvisepalum as revealed by high-throughput sequencing and fluorescent in situ hybridization
author_facet Lee, Yung-I
Yap, Jing Wei
Ramlee, Shairul Izan
Leitch, Ilia J.
Fay, Michael F.
Lee, Yi-Ching
Hidalgo, Oriane
Dodsworth, Steven
Smulders, Marinus J. M.
Gravendeel, Barbara
Leitch, Andrew R.
author_sort Lee, Yung-I
title Satellite DNA in Paphiopedilum subgenus Parvisepalum as revealed by high-throughput sequencing and fluorescent in situ hybridization
title_short Satellite DNA in Paphiopedilum subgenus Parvisepalum as revealed by high-throughput sequencing and fluorescent in situ hybridization
title_full Satellite DNA in Paphiopedilum subgenus Parvisepalum as revealed by high-throughput sequencing and fluorescent in situ hybridization
title_fullStr Satellite DNA in Paphiopedilum subgenus Parvisepalum as revealed by high-throughput sequencing and fluorescent in situ hybridization
title_full_unstemmed Satellite DNA in Paphiopedilum subgenus Parvisepalum as revealed by high-throughput sequencing and fluorescent in situ hybridization
title_sort satellite dna in paphiopedilum subgenus parvisepalum as revealed by high-throughput sequencing and fluorescent in situ hybridization
publisher BioMed Central
publishDate 2018
url http://psasir.upm.edu.my/id/eprint/73825/1/FISH.pdf
http://psasir.upm.edu.my/id/eprint/73825/
https://pubmed.ncbi.nlm.nih.gov/30068293/
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