Innovation to turn 'junk DNA' into genetic markers

Innovation to turn ‘junk DNAs’ into genetic markers
High-throughput sequencing of retrotransposon insertion sites and its applications.

A series of the Next-Generation Sequencer (NGS) applications are being developed to utilize 'junk DNA' as distinctive genetic analysis systems for crop species.

Many nucleic DNAs do not have any known biological functions. Such DNAs are referred to as 'junk DNAs'. Having accumulated genomic copies throughout evolution, retrotransposons constitute a major portion of junk DNAs. Although most copies have lost copy-making ability, small groups of the retrotransposons still remain competent. The copies of an active group are inserted at markedly different genomic positions, even among closely related varieties of the .

Identification of the active groups is, however, challenging as they are concealed by numerous non-active groups. Additionally, DNA sequences of the numerous positions where active groups are inserted must be efficiently determined for genetic population under study.

Yuki Monden and colleagues at Okayama University, National Institute of Genetics, and Tochigi and Fukuoka Prefectural Agricultural Research Stations have prepared the NGS (HiSeq2000) sequence library of strawberry, which exclusively contains terminal sequences of a major retrotransposon type (LTR: Long Terminal Repeat), and have successfully identified the active groups using novel NGS sequence analysis.

In another study, the insertion site library for two active groups was constructed over 38 sweet potato varieties. The NGS analysis determined 2024 inserted positions, of which 91.4% occurred in a single variety or varieties of different combination.

The series of NGS applications on active provide efficient genetic analysis systems, especially for variety fingerprinting, linkage map construction, and lineage analysis of the crop species.

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More information: Yuki Monden, Nobuyuki Fujii, Kentaro Yamaguchi, Kazuho Ikeo, Yoshiko Nakazawa, Takamitsu Waki, Keita Hirashima, Yosuke Uchimura, Makoto Tahara. "Efficient screening of long terminal repeat retrotransposons that show high insertion polymorphism via high-throughput sequencing of the primer binding site." Genome, (2014). (DOI): 10.1139/gen-2014-0031

Yuki Monden, Ayaka Yamamoto, Akiko Shindo, and Makoto Tahara. "Efficient DNA Fingerprinting Based on the Targeted Sequencing of Active Retrotransposon Insertion Sites Using a Bench-Top High-Throughput Sequencing Platform." DNA Research, (2014). (DOI): 10.1093/dnares/dsu015

Provided by Okayama University
Citation: Innovation to turn 'junk DNA' into genetic markers (2014, September 30) retrieved 27 January 2020 from
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