作物学报 ›› 2023, Vol. 49 ›› Issue (2): 414-425.doi: 10.3724/SP.J.1006.2023.24022
潘洁明1(
), 田绍锐3, 梁艳兰2, 朱宇林1, 周定港4, 阙友雄2, 凌辉1,*(
), 黄宁1,*(
)
PAN Jie-Ming1(
), TIAN Shao-Rui3, LIANG Yan-Lan2, ZHU Yu-Lin1, ZHOU Ding-Gang4, QUE You-Xiong2, LING Hui1,*(
), HUANG Ning1,*(
)
摘要:
PILS (PIN-LIKES)是一类新发现的生长素输出载体, 协助生长素的极性运输。本研究立足甘蔗割手密基因组和栽培品种转录组数据, 利用生物信息学分析技术, 分别在割手密和栽培品种中鉴定到11个PILS (Saccharum spontaneum PIN-LIKES, SsPILS )基因和4个PILS (Saccharum spp. hybrid PIN-LIKES, ScPILS)基因。结果表明, 11个SsPILS基因家族成员分布于6条染色体上, 基因内含子数量介于5~11个。系统进化树分析发现, 割手密PILS与水稻PILS有较高同源性, 归属于3个不同的系统发育分支。转录组数据分析显示, SsPILS1c的同源基因ScPILS1c在受高粱花叶病毒和黑穗病菌胁迫甘蔗栽培种中差异表达。通过RT-PCR扩增技术, 克隆获得ScPILS1c基因序列(NCBI accession number: OM258732)。该基因全长cDNA为1332 bp, 包含一个1233 bp的完整开放阅读框, 编码410个氨基酸, 理论等电点(pI)为6.17, 不稳定系数为39.31, 平均疏水性值为0.689, 预测ScPILS1c为稳定酸性疏水蛋白。其编码蛋白的二级结构主要包括α-螺旋(48.54%)和无规则卷曲(35.37%), 这与三级结构预测结果相符。qRT-PCR表达分析揭示, ScPILS1c基因在甘蔗中的表达具有组织特异性, 在蔗髓中表达量最低、皮中的表达量最高, 同时该基因的表达受H2O2及黑穗病菌的显著性诱导。亚细胞定位表明, ScPILS1c基因的编码蛋白主要定位于细胞膜。以上结果为深入研究甘蔗PIN-LIKES基因的结构和功能积累了基础资料。
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