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Genome-wide identification, molecular evolution and expression analysis of the non-specific lipid transfer protein (nsLTP) family in Setaria italica.
Li, Feng; Fan, Kai; Guo, Xuhu; Liu, Jianxia; Zhang, Kun; Lu, Ping.
Afiliación
  • Li F; College of Agronomy and Life Sciences, Shanxi Datong University, Datong, 037009, China. LF_sxdtdx@163.com.
  • Fan K; Research and Development Center of Agricultural Facility Technology, Shanxi Datong University, Datong, 037009, China. LF_sxdtdx@163.com.
  • Guo X; Key Laboratory of Ministry of Education for Genetics, Breeding and Multiple Utilization of Crops, College of Crop Science, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.
  • Liu J; College of Agronomy and Life Sciences, Shanxi Datong University, Datong, 037009, China.
  • Zhang K; Research and Development Center of Agricultural Facility Technology, Shanxi Datong University, Datong, 037009, China.
  • Lu P; College of Agronomy and Life Sciences, Shanxi Datong University, Datong, 037009, China.
BMC Plant Biol ; 22(1): 547, 2022 Nov 28.
Article en En | MEDLINE | ID: mdl-36443672
ABSTRACT

BACKGROUND:

Foxtail millet (Setaria italica L.) is a millet species with high tolerance to stressful environments. Plant non-specific lipid transfer proteins (nsLTPs) are a kind of small, basic proteins involved in many biological processes. So far, the genome of S. italica has been fully sequenced, and a comprehensive understanding of the evolution and expression of the nsLTP family is still lacking in foxtail millet.

RESULTS:

Forty-five nsLTP genes were identified in S. italica and clustered into 5 subfamilies except three single genes (SinsLTP38, SinsLTP7, and SinsLTP44). The proportion of SinsLTPs was different in each subfamily, and members within the same subgroup shared conserved exon-intron structures. Besides, 5 SinsLTP duplication events were investigated. Both tandem and segmental duplication contributed to nsLTP expansion in S. italica, and the duplicated SinsLTPs had mainly undergone purifying selection pressure, which suggested that the function of the duplicated SinsLTPs might not diverge much. Moreover, we identified the nsLTP members in 5 other monocots, and 41, 13, 10, 4, and 1 orthologous gene pairs were identified between S. italica and S. viridis, S. bicolor, Z. mays, O. sativa, and B. distachyon, respectively. The functional divergence within the nsLTP orthologous genes might be limited. In addition, the tissue-specific expression patterns of the SinsLTPs were investigated, and the expression profiles of the SinsLTPs in response to abiotic stress were analyzed, all the 10 selected SinsLTPs were responsive to drought, salt, and cold stress. Among the selected SinsLTPs, 2 paired duplicated genes shared almost equivalent expression profiles, suggesting that these duplicated genes might retain some essential functions during subsequent evolution.

CONCLUSIONS:

The present study provided the first systematic analysis for the phylogenetic classification, conserved domain and gene structure, expansion pattern, and expression profile of the nsLTP family in S. italica. These findings could pave a way for further comparative genomic and evolution analysis of nsLTP family in foxtail millet and related monocots, and lay the foundation for the functional analysis of the nsLTPs in S. italica.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Setaria (Planta) Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Revista: BMC Plant Biol Asunto de la revista: BOTANICA Año: 2022 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Setaria (Planta) Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Revista: BMC Plant Biol Asunto de la revista: BOTANICA Año: 2022 Tipo del documento: Article País de afiliación: China
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