Pathogenesis-related protein-4 (PR-4) gene family in Qingke (Hordeum vulgare L. var. nudum): genome-wide identification, structural analysis and expression profile under stresses
文献类型: 外文期刊
第一作者: Wang, Le
作者: Wang, Le;Shang, Qianhan;Yin, Wei;Sa, Wei;Liang, Jian;Wang, Le;Lu, Hailing;Zhan, Jiarong;Shang, Qianhan;Liang, Jian;Wang, Le;Shang, Qianhan;Wang, Li;Liang, Jian
作者机构:
关键词: Tibetan hulless barley; Plant immunity; PR-4 family gene; Expression profile
期刊名称:MOLECULAR BIOLOGY REPORTS ( 影响因子:2.742; 五年影响因子:2.702 )
ISSN: 0301-4851
年卷期: 2022 年 49 卷 10 期
页码:
收录情况: SCI
摘要: Background Pathogenesis-related (PR) proteins are active participants of plant defense against biotic and abiotic stresses. The PR-4 family features a Barwin domain at the C-terminus, which endows the host plant with disease resistance. However, comprehensive analysis of PR-4 genes is still lacking in Qingke (Hordeum vulgare L. var. nudum). Methods and results Herein, a total of four PR-4 genes were identified from the genome of Qingke through HMM profiling. Devoid of the chitin-binding domain, these 4 proteins were grouped as class II PR-4s. Phylogenic analysis revealed that 127 PR-4s from 47 species were clustered into 3 major groups, among which the four Qingke PR-4s were claded into group I. Analysis of gene structure demonstrated that no intron was found in 3 out of the 4 Qingke PR-4s, and HOVUSG0928500 was the only gene contained one intron. An array of cis-acting motifs were detected in promoters of Qingke PR-4 genes, including elements associated with hormone response, light response, stress response, growth and development processes and binding sites of transcription factors, implying their diverse role. Expression profiling confirmed that Qingke PR-4s were involved in defense response against drought, cold and powdery mildews infection, and transcription of HOVUSG1974300 and HOVUSG5705400 was differentially regulated by MeJA and SA. Conclusion Findings of the study provided insights into the genetic basis of the PR-4 family genes, and would promote further investigation on protein function and utilization.
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