| Literature DB >> 34554437 |
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.Entities:
Keywords: Cleistogenes songorica; Identification; LTR retrotransposon; Molecular marker; Polymorphism; Transferability
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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