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Year 2021, , 1 - 12, 30.06.2021
https://doi.org/10.53447/communc.820287

Abstract

References

  • Hillis, D.M., Dixon M. T., Ribosomal DNA: molecular evolution and phylogenetic inference, The Quarterly review of biology, 66 (4) (1991), 411-453.
  • Warwick, S.I., Mummenhoff, K., Sauder, C.A., Koch, M.A., Al-Shehbaz, I.A., Closing the gaps: phylogenetic relationships in the Brassicaceae based on DNA sequence data of nuclear ribosomal ITS region, Plant Systematics and Evolution, 285 (3-4) (2010), 209-232. https://doi.org/10.1007/s00606-010-0271-8.
  • Baldwin, B. G., Sanderson, M. J., Porter, J. M., Wojciechowski, M. F., Campbell, C. S., Donoghue, M. J., The ITS region of nuclear ribosomal DNA: a valuable source of evidence on angiosperm phylogeny, Annals of the Missouri Botanical Garden, (1995), 247-277.
  • Musters, W., Boon, K., Van der Sande, C. A., van Heerikhuizen, H., & Planta, R. J., Functional analysis of transcribed spacers of yeast ribosomal DNA, The EMBO journal, 9 (12) (1990), 3989-3996. https://doi.org/10.1002/j.1460-2075.1990.tb07620.x
  • Mai, J. C., Coleman, A. W., The internal transcribed spacer 2 exhibits a common secondary structure in green algae and flowering plants, Journal of Molecular Evolution, 44 (3) (1997), 258-271.
  • Coleman, A. W., Is there a molecular key to the level of “biological species” in eukaryotes? A DNA guide, Molecular phylogenetics and evolution, 50(1) (2009), 197-203. https://doi.org/10.1016/j.ympev.2008.10.008.
  • Wolf, M., Chen, S., Song, J., Ankenbrand, M., Müller, T., Compensatory base changes in ITS2 secondary structures correlate with the biological species concept despite intragenomic variability in ITS2 sequences–a proof of concept, PloS one,8(6) (2013), e66726. https://doi.org/10.1371/journal.pone.0066726.
  • Coleman, A. W., Vacquier, V. D., Exploring the phylogenetic utility of ITS sequences for animals: a test case for abalone (Haliotis), Journal of molecular evolution, 54(2) (2002), 246-257. https://doi.org/ 10.1007/s00239-001-0006-0.
  • Mullineux, T., Hausner, G., Evolution of rDNA ITS1 and ITS2 sequences and RNA secondary structures within members of the fungal genera Grosmannia and Leptographium, Fungal Genetics and Biology, 46(11) (2009), 855-867. https://doi.org/10.1016/j.fgb.2009.08.001.
  • Saha, P. S., Sengupta, M., Jha, S., Ribosomal DNA ITS1, 5.8 S and ITS2 secondary structure, nuclear DNA content and phytochemical analyses reveal distinctive characteristics of four subclades of Protasparagus, Journal of Systematics and Evolution, 55(1) (2017), 54-70. https://doi.org/10.1111/jse.12221.
  • Karpenko, N., Martyniuk, V., Tyshchenko, O., Tarieiev, A., Tekpınar, A., Didenko, V., Kostikov, I., Resolving the position of Astragalus borysthenicus Klokov within the Astragalus L. species, Turkish Journal of Botany, 42(5) (2018), 623-635. https://doi.org/10.3906/bot-1712-52.
  • Liu, J. S., Schardl, C. L., A conserved sequence in internal transcribed spacer 1 of plant nuclear rRNA genes, Plant molecular biology, 26(2) (1994), 775-778.
  • Nues, R. W., Rientjes, J. M., van der Sande, C. A., Zerp, S. F., Sluiter, C., Venema, J., Planta, R. J., RauØ, H. A., Separate structural elements within internal transcribed spacer 1 of Saccharomyces cerevisiae precursor ribosomal RNA direct the formation of 17S and 26S rRNA, Nucleic acids research, 22(6) (1994), 912-919. https://doi.org/10.1093/nar/22.6.912.
  • Rampersad, S. N., ITS1, 5.8 S and ITS2 secondary structure modelling for intra-specific differentiation among species of the Colletotrichum gloeosporioides sensu lato species complex, Springer Plus 3(1) (2014), 684. https://doi.org/10.1186/2193-1801-3-684.
  • Meyer, F.K., Conspectus der “Thlaspi”-Arten Europas, Afrikas und Vorderasiens., Feddes Repertorium, 84 (1973) 449-469.
  • Meyer, F.K., Kritische Revision der Thlaspi ︁‐Arten Europas, Afrikas und Vorderasiens I. Geschichte, Morphologie und Chorologie, Feddes Repertorium, 90(3) (1979), 129-154.
  • Ali, T., Schmuker, A., Runge, F., Solovyeva, I., Nigrelli, L., Paule, J., Buch, A.N., Xia, X., Ploch, S., Orren, O., Kummer, V., Linde-Laursen, I., Ҫelik, A., Thines, M., Morphology, phylogeny, and taxonomy of Microthlaspi (Brassicaceae: Coluteocarpeae) and related genera., Taxon, 65(1) (2016), 79-98. http://dx.doi.org/ 10.12705/651.6.
  • https://brassibase.cos.uni-heidelberg.de/, accessed 02 November 2020.
  • Al-Shehbaz, I. A., A synopsis of the genus Noccaea (Coluteocarpeae, Brassicaceae), Harvard papers in Botany 19(1) (2014), 25-51. https://doi.org/10.3100/hpib.v19iss1. 2014.n3.
  • Özüdoğru, B., Özgişi, K., Tarıkahya-Hacıoğlu, B., Ocak, A., Mummenhoff, K., Al-Shehbaz, I. A., Phylogeny of the Genus Noccaea (Brassicaceae) and a Critical Review of Its Generic Circumscription1, 2, Annals of the Missouri Botanical Garden, 104(3) (2019), 339-354. https://doi.org/10.3417/2019347.
  • Greuter, W, Raus, T, Med-checklist notulae 7., Willdenowia (1983), 79-99.
  • Greuter, W., Burdet, H. M., Long, G., Med-checklist, Conservatoire et Jardin Botaniques de la Ville de Genève, Ginebra, vol. 3, (1986).
  • Al-Shehbaz, I.A., The genera of Lepidieae (cruciferae; Brassicaceae) in the southeastern United States., Journal of the Arnold Arboretum, 67(3) (1986), 265-311.
  • Özgişi, K. Structural characterization of ITS2 and CBC species concept applications in the tribe Coluteocarpeae (Brassicaceae), Turkish Journal of Botany, 44(3) (2020), 295-308. http://dx.doi.org/10.3906/bot-1911-4.
  • Meyer, F. K.. Kritische Revision der “Thlaspi”-Arten Europas, Afrikas und Vorderasiens, Spezieller Tiel, VIII. Raparia F.K.Mey, Haussknechtia 11(2006), 195–206.
  • White, T. J., Bruns, T., S. L., Taylor, J., Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics., PCR protocols: a guide to methods and applications, 18(1) (1990), 315-322.
  • Warwick, S. I., Al-Shehbaz, I. A., Sauder, C.A., Murray, D. F., Mummenhoff, K., Phylogeny of Smelowskia and related genera (Brassicaceae) based on nuclear ITS DNA and chloroplast trnL intron DNA sequences, Annals of the Missouri Botanical Garden, (2004), 99-123.
  • Edgar, R.C., MUSCLE: multiple sequence alignment with high accuracy and high throughput., Nucleic acids research, 32(5) (2004), 1792-1797. https://doi.org/10.1093/ nar/gkh340.
  • Zuker, M., Mfold web server for nucleic acid folding and hybridization prediction, Nucleic acids research, 31(13) (2003), 3406-3415. https://doi.org/10.1093/nar/gkg595.
  • Xia, T., Mathews, D.H., Turner, D.H., Thermodynamics of RNA secondary structure formation, RNA, (2001), 21-48.
  • Edger, P. P., Tang, M., Bird, K. A., Mayfield, D. R., Conant, G., Mummenhoff, K., Koch, M.A., Pires, J.C., Secondary structure analyses of the nuclear rRNA internal transcribed spacers and assessment of its phylogenetic utility across the Brassicaceae (Mustards)., PloS one 9(7) (2014), e101341. https://doi.org/10.1371/ journal.pone.010 1341.
  • Slotta, T.A.B., Phylogenetic analysis of Iliamna (Malvaceae) using the Internal Transcribed Spacer region. Virginia Polytechnic Institute and State University, Thesis, (2000).

CHARACTERIZATION OF ITS1 SECONDARY STRUCTURE IN TEN SPECIES OF COLUTEOCARPEAE (BRASSICACEAE) AND ITS TAXONOMICAL UTILITY

Year 2021, , 1 - 12, 30.06.2021
https://doi.org/10.53447/communc.820287

Abstract

Utility of the internal transcribed spacers (ITSs) of ribosomal RNA sequences to infer phylogenetic relationships among organisms have been proven. Although ITS1 and ITS2 are highly variable in sequence, they have conserved structures that have a key function in the processing of rRNA gene transcripts. Determining of such a conserved motif can help to identify relationships between organisms. Since ITS2 has much more conserved secondary structure, structural properties of ITS1 are generally neglected by researchers. In this study, ITS1 secondary structures of ten representative species, which were once assigned under different genera, of tribe Coluteocarpeae were determined. Also taxonomical utility of ITS1 secondary structure was also tested. Analyses indicate that there are four different types (4-, 6-, 7- and 8 hairpin) of secondary structures. On the other hand, each sequences have a conserved region that is common among land plants. Since previous studies reveals other species, that belong different tribes or lineages of Brassicaceae show similar ITS1 secondary structure, it is not a useful delimitation tool for investigated species in terms of taxonomy.

References

  • Hillis, D.M., Dixon M. T., Ribosomal DNA: molecular evolution and phylogenetic inference, The Quarterly review of biology, 66 (4) (1991), 411-453.
  • Warwick, S.I., Mummenhoff, K., Sauder, C.A., Koch, M.A., Al-Shehbaz, I.A., Closing the gaps: phylogenetic relationships in the Brassicaceae based on DNA sequence data of nuclear ribosomal ITS region, Plant Systematics and Evolution, 285 (3-4) (2010), 209-232. https://doi.org/10.1007/s00606-010-0271-8.
  • Baldwin, B. G., Sanderson, M. J., Porter, J. M., Wojciechowski, M. F., Campbell, C. S., Donoghue, M. J., The ITS region of nuclear ribosomal DNA: a valuable source of evidence on angiosperm phylogeny, Annals of the Missouri Botanical Garden, (1995), 247-277.
  • Musters, W., Boon, K., Van der Sande, C. A., van Heerikhuizen, H., & Planta, R. J., Functional analysis of transcribed spacers of yeast ribosomal DNA, The EMBO journal, 9 (12) (1990), 3989-3996. https://doi.org/10.1002/j.1460-2075.1990.tb07620.x
  • Mai, J. C., Coleman, A. W., The internal transcribed spacer 2 exhibits a common secondary structure in green algae and flowering plants, Journal of Molecular Evolution, 44 (3) (1997), 258-271.
  • Coleman, A. W., Is there a molecular key to the level of “biological species” in eukaryotes? A DNA guide, Molecular phylogenetics and evolution, 50(1) (2009), 197-203. https://doi.org/10.1016/j.ympev.2008.10.008.
  • Wolf, M., Chen, S., Song, J., Ankenbrand, M., Müller, T., Compensatory base changes in ITS2 secondary structures correlate with the biological species concept despite intragenomic variability in ITS2 sequences–a proof of concept, PloS one,8(6) (2013), e66726. https://doi.org/10.1371/journal.pone.0066726.
  • Coleman, A. W., Vacquier, V. D., Exploring the phylogenetic utility of ITS sequences for animals: a test case for abalone (Haliotis), Journal of molecular evolution, 54(2) (2002), 246-257. https://doi.org/ 10.1007/s00239-001-0006-0.
  • Mullineux, T., Hausner, G., Evolution of rDNA ITS1 and ITS2 sequences and RNA secondary structures within members of the fungal genera Grosmannia and Leptographium, Fungal Genetics and Biology, 46(11) (2009), 855-867. https://doi.org/10.1016/j.fgb.2009.08.001.
  • Saha, P. S., Sengupta, M., Jha, S., Ribosomal DNA ITS1, 5.8 S and ITS2 secondary structure, nuclear DNA content and phytochemical analyses reveal distinctive characteristics of four subclades of Protasparagus, Journal of Systematics and Evolution, 55(1) (2017), 54-70. https://doi.org/10.1111/jse.12221.
  • Karpenko, N., Martyniuk, V., Tyshchenko, O., Tarieiev, A., Tekpınar, A., Didenko, V., Kostikov, I., Resolving the position of Astragalus borysthenicus Klokov within the Astragalus L. species, Turkish Journal of Botany, 42(5) (2018), 623-635. https://doi.org/10.3906/bot-1712-52.
  • Liu, J. S., Schardl, C. L., A conserved sequence in internal transcribed spacer 1 of plant nuclear rRNA genes, Plant molecular biology, 26(2) (1994), 775-778.
  • Nues, R. W., Rientjes, J. M., van der Sande, C. A., Zerp, S. F., Sluiter, C., Venema, J., Planta, R. J., RauØ, H. A., Separate structural elements within internal transcribed spacer 1 of Saccharomyces cerevisiae precursor ribosomal RNA direct the formation of 17S and 26S rRNA, Nucleic acids research, 22(6) (1994), 912-919. https://doi.org/10.1093/nar/22.6.912.
  • Rampersad, S. N., ITS1, 5.8 S and ITS2 secondary structure modelling for intra-specific differentiation among species of the Colletotrichum gloeosporioides sensu lato species complex, Springer Plus 3(1) (2014), 684. https://doi.org/10.1186/2193-1801-3-684.
  • Meyer, F.K., Conspectus der “Thlaspi”-Arten Europas, Afrikas und Vorderasiens., Feddes Repertorium, 84 (1973) 449-469.
  • Meyer, F.K., Kritische Revision der Thlaspi ︁‐Arten Europas, Afrikas und Vorderasiens I. Geschichte, Morphologie und Chorologie, Feddes Repertorium, 90(3) (1979), 129-154.
  • Ali, T., Schmuker, A., Runge, F., Solovyeva, I., Nigrelli, L., Paule, J., Buch, A.N., Xia, X., Ploch, S., Orren, O., Kummer, V., Linde-Laursen, I., Ҫelik, A., Thines, M., Morphology, phylogeny, and taxonomy of Microthlaspi (Brassicaceae: Coluteocarpeae) and related genera., Taxon, 65(1) (2016), 79-98. http://dx.doi.org/ 10.12705/651.6.
  • https://brassibase.cos.uni-heidelberg.de/, accessed 02 November 2020.
  • Al-Shehbaz, I. A., A synopsis of the genus Noccaea (Coluteocarpeae, Brassicaceae), Harvard papers in Botany 19(1) (2014), 25-51. https://doi.org/10.3100/hpib.v19iss1. 2014.n3.
  • Özüdoğru, B., Özgişi, K., Tarıkahya-Hacıoğlu, B., Ocak, A., Mummenhoff, K., Al-Shehbaz, I. A., Phylogeny of the Genus Noccaea (Brassicaceae) and a Critical Review of Its Generic Circumscription1, 2, Annals of the Missouri Botanical Garden, 104(3) (2019), 339-354. https://doi.org/10.3417/2019347.
  • Greuter, W, Raus, T, Med-checklist notulae 7., Willdenowia (1983), 79-99.
  • Greuter, W., Burdet, H. M., Long, G., Med-checklist, Conservatoire et Jardin Botaniques de la Ville de Genève, Ginebra, vol. 3, (1986).
  • Al-Shehbaz, I.A., The genera of Lepidieae (cruciferae; Brassicaceae) in the southeastern United States., Journal of the Arnold Arboretum, 67(3) (1986), 265-311.
  • Özgişi, K. Structural characterization of ITS2 and CBC species concept applications in the tribe Coluteocarpeae (Brassicaceae), Turkish Journal of Botany, 44(3) (2020), 295-308. http://dx.doi.org/10.3906/bot-1911-4.
  • Meyer, F. K.. Kritische Revision der “Thlaspi”-Arten Europas, Afrikas und Vorderasiens, Spezieller Tiel, VIII. Raparia F.K.Mey, Haussknechtia 11(2006), 195–206.
  • White, T. J., Bruns, T., S. L., Taylor, J., Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics., PCR protocols: a guide to methods and applications, 18(1) (1990), 315-322.
  • Warwick, S. I., Al-Shehbaz, I. A., Sauder, C.A., Murray, D. F., Mummenhoff, K., Phylogeny of Smelowskia and related genera (Brassicaceae) based on nuclear ITS DNA and chloroplast trnL intron DNA sequences, Annals of the Missouri Botanical Garden, (2004), 99-123.
  • Edgar, R.C., MUSCLE: multiple sequence alignment with high accuracy and high throughput., Nucleic acids research, 32(5) (2004), 1792-1797. https://doi.org/10.1093/ nar/gkh340.
  • Zuker, M., Mfold web server for nucleic acid folding and hybridization prediction, Nucleic acids research, 31(13) (2003), 3406-3415. https://doi.org/10.1093/nar/gkg595.
  • Xia, T., Mathews, D.H., Turner, D.H., Thermodynamics of RNA secondary structure formation, RNA, (2001), 21-48.
  • Edger, P. P., Tang, M., Bird, K. A., Mayfield, D. R., Conant, G., Mummenhoff, K., Koch, M.A., Pires, J.C., Secondary structure analyses of the nuclear rRNA internal transcribed spacers and assessment of its phylogenetic utility across the Brassicaceae (Mustards)., PloS one 9(7) (2014), e101341. https://doi.org/10.1371/ journal.pone.010 1341.
  • Slotta, T.A.B., Phylogenetic analysis of Iliamna (Malvaceae) using the Internal Transcribed Spacer region. Virginia Polytechnic Institute and State University, Thesis, (2000).
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Details

Primary Language English
Subjects Structural Biology
Journal Section Research Articles
Authors

Kurtuluş Özgişi 0000-0002-7344-6666

Publication Date June 30, 2021
Acceptance Date December 8, 2020
Published in Issue Year 2021

Cite

Communications Faculty of Sciences University of Ankara Series C-Biology.

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