Literature DB >> 34554437

Development of molecular markers based on LTR retrotransposon in the Cleistogenes songorica genome.

Tiantian Ma1, Xingyi Wei1, Yufei Zhang1, Jie Li1, Fan Wu1, Qi Yan1, Zhuanzhuan Yan1, Zhengshe Zhang1, Gisele Kanzana1, Yufeng Zhao1, Yingbo Yang1, Jiyu Zhang2.   

Abstract

Long terminal repeat retrotransposons (LTR-RTs) contribute a large fraction of many sequenced plant genomes and play important roles in genomic diversity and phenotypic variations. LTR-RTs are abundantly distributed in plant genomes, facilitating the development of markers based on LTR-RTs for a variety of genotyping purposes. Whole-genome analysis of LTR-RTs was performed in Cleistogenes songorica. A total of 299,079 LTR-RTs were identified and classified as Gypsy type, Copia type, or other type. LTR-RTs were widely distributed in the genome, enriched in the heterochromatic region of the chromosome, and negatively correlated with gene distribution. However, approximately one-fifth of genes were still interrupted by LTR-RTs, and these genes are annotated. Furthermore, four types of primer pairs (PPs) were designed, namely, retrotransposon-based insertion polymorphisms, inter-retrotransposon amplified polymorphisms, insertion site-based polymorphisms, and retrotransposon-microsatellite amplified polymorphisms. A total of 350 PPs were screened in 23 accessions of the genus Cleistogenes, of which 80 PPs showed polymorphism, and 72 PPs showed transferability among Gramineae and non-Gramineae species. In addition, a comparative analysis of homologous LTR-RTs was performed with other related grasses. Taken together, the study will serve as a valuable resource for genotyping applications for C. songorica and related grasses.
© 2021. Institute of Plant Genetics, Polish Academy of Sciences, Poznan.

Entities:  

Keywords:  Cleistogenes songorica; Identification; LTR retrotransposon; Molecular marker; Polymorphism; Transferability

Mesh:

Substances:

Year:  2021        PMID: 34554437     DOI: 10.1007/s13353-021-00658-9

Source DB:  PubMed          Journal:  J Appl Genet        ISSN: 1234-1983            Impact factor:   3.240


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