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Gene Deletion in Barley Mediated by LTR-retrotransposon BARE
Author(s) -
Yi Shang,
Fei Yang,
Alan H. Schulman,
Jinghuan Zhu,
Yong Jia,
Junmei Wang,
Xiaoqi Zhang,
Qiaojun Jia,
Wei Hua,
Jianming Yang,
Chengdao Li
Publication year - 2017
Publication title -
scientific reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.24
H-Index - 213
ISSN - 2045-2322
DOI - 10.1038/srep43766
Subject(s) - retrotransposon , genetics , biology , gene , long terminal repeat , transposable element , mutant , genomic dna , recombination , genome
A poly-row branched spike ( prbs ) barley mutant was obtained from soaking a two-rowed barley inflorescence in a solution of maize genomic DNA. Positional cloning and sequencing demonstrated that the prbs mutant resulted from a 28 kb deletion including the inflorescence architecture gene HvRA2 . Sequence annotation revealed that the HvRA2 gene is flanked by two LTR (long terminal repeat) retrotransposons ( BARE ) sharing 89% sequence identity. A recombination between the integrase (IN) gene regions of the two BARE copies resulted in the formation of an intact BARE and loss of HvRA2. No maize DNA was detected in the recombination region although the flanking sequences of HvRA2 gene showed over 73% of sequence identity with repetitive sequences on 10 maize chromosomes. It is still unknown whether the interaction of retrotransposons between barley and maize has resulted in the recombination observed in the present study.

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