# Using quantitative PCR with retrotransposon-based insertion polymorphisms as markers in sugarcane

**Authors:** Cushla J. Metcalfe, Sarah G. Oliveira, Jonas W. Gaiarsa, Karen S. Aitken, Monalisa S. Carneiro, Fernanda Zatti, Marie-Anne Van Sluys

PMC · DOI: 10.1093/jxb/erv283 · Journal of Experimental Botany · 2015-06-19

## TL;DR

Researchers developed a new method using qPCR and transposable elements to study sugarcane genetics and evolution.

## Contribution

A novel genotyping method using transposable elements was developed for sugarcane and related species.

## Key findings

- The qPCR-RBIP method can be used as part of a genotyping system for sugarcane.
- Three transposable elements were found only in one lineage of modern sugarcane cultivars.
- The transposable elements support the current understanding of sugarcane evolution.

## Abstract

qPCR-RBIP was used to examine the dosage of particular markers and evolutionary history in Saccharum and the related genera, Erianthus and Miscanthus. It also differentiated between S. spontaneum and S. officinarum.

Sugarcane is the main source of the world’s sugar and is becoming increasingly important as a source of biofuel. The highly polyploid and heterozygous nature of the sugarcane genome has meant that characterization of the genome has lagged behind that of other important crops. Here we developed a method using a combination of quantitative PCR with a transposable marker system to score the relative number of alleles with a transposable element (TE) present at a particular locus. We screened two genera closely related to Saccharum (Miscanthus and Erianthus), wild Saccharum, traditional cultivars, and 127 modern cultivars from Brazilian and Australian breeding programmes. We showed how this method could be used in various ways. First, we showed that the method could be extended to be used as part of a genotyping system. Secondly, the history of insertion and timing of the three TEs examined supports our current understanding of the evolution of the Saccharum complex. Thirdly, all three TEs were found in only one of the two main lineages leading to the modern sugarcane cultivars and are therefore the first TEs identified that could potentially be used as markers for Saccharum spontaneum.

## Linked entities

- **Species:** Saccharum (taxon 4546), Erianthus (taxon 323203), Miscanthus (taxon 62336)

## Full-text entities

- **Genes:** tga1 [NCBI Gene 103653213]
- **Diseases:** TSD (MESH:D009371), LTR-RT (MESH:C563738), TE (MESH:C565217)
- **Chemicals:** CTAB (MESH:D000077286), SP (MESH:C000604007), sucrose (MESH:D013395), sugar (MESH:D000073893), lipids (MESH:D008055), starch (MESH:D013213), halogen (MESH:D006219), Bioethanol (-),  (MESH:D005819)
- **Species:** Saccharum barberi (Indian cane, species) [taxon 152679], Zea mays (maize, species) [taxon 4577], Erianthus (genus) [taxon 323203], S. bicolor [taxon 381118], Saccharum sinense (species) [taxon 154766], Saccharum spontaneum (fodder cane, species) [taxon 62335], Saccharum officinarum (noble cane, species) [taxon 4547], Saccharum robustum (species) [taxon 62334], Oryza sativa (Asian cultivated rice, species) [taxon 4530], Sorghum bicolor (broomcorn, species) [taxon 4558], Miscanthus (silver grass, genus) [taxon 62336]
- **Cell lines:** SCHRBa_011_K15 — Homo sapiens (Human), Induced pluripotent stem cell (CVCL_A7JR), S2 — Drosophila melanogaster (Fruit fly), Spontaneously immortalized cell line (CVCL_Z232), SCHRBa_044_D02 — Homo sapiens (Human), Finite cell line (CVCL_H953)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC4493790/full.md

## References

69 references — full list in the complete paper: https://tomesphere.com/paper/PMC4493790/full.md

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Source: https://tomesphere.com/paper/PMC4493790