南美超级胎牛血清999尝鲜特惠
转染试剂低至5折
基质胶阶梯特惠
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南美超级胎牛血清999尝鲜特惠
转染试剂低至5折
基质胶阶梯特惠
积分商城,好礼送不停
分子生物学
IVD分子诊断
细胞培养与分析
蛋白研究
细胞因子
重组蛋白
抗体
高通量测序建库
病原检测UCF系列
生物医药
工具酶
抑制剂激活剂与常用试剂
仪器
耗材

染色体加倍与增强的自交相容性以及枸杞花粉与柱头相互作用的转录重塑有关。

Chromosome doubling is associated with enhanced self-compatibility and transcriptional remodeling of pollen–pistil interactions in Lycium chinense

Wang Zixuan, Qin Yingzhi, Qin Ken, Zhang Bo, Chen Jinhuan

Journal:PLANT CELL REPORTS

IF:5.3

DOI:10.1007/s00299-026-03991-7

PMID:

Published:2026-09-23

research field:药理学内分泌学生殖毒理学皮肤科衰老研究

Abstract

Key message Cytology and 72-sample pistil transcriptomes link chromosome doubling to self-compatibility in autotetraploid Lycium chinense through altered pollen–pistil responses and candidate S-RNase trafficking and detoxification pathways. Polyploidy can reshape plant reproductive traits and self-compatibility systems, yet the mechanisms underlying ploidy-associated transitions to self-compatibility remain poorly understood. In this study, diploid and autotetraploid Lycium chinense were compared using floral morphology, stigma receptivity, pollen viability, and pollen tube cytology, controlled pollination, seed vigor analysis, and transcriptome sequencing of 72 pistil samples spanning stigma, style, and ovary tissues at four pollination stages. Chromosome doubling enlarged reproductive organs, prolonged stigma receptivity, and increased pollen size, while also altering pollen performance and pollen tube growth. Diploid self-pollen tubes were arrested in the upper style, whereas autotetraploid self-pollen tubes continued through the style, accompanied by a marked increase in self-compatibility, with the compatibility index rising from 0.50 to 5.70 and fruit set from 8.33% to 73.33%. Spatiotemporal transcriptome analysis revealed extensive tissue- and time-dependent transcriptional remodeling between ploidy levels. Temporal clustering and ploidy × time interaction analyses showed particularly pronounced divergence in the stigma and style, with the style exhibiting the strongest interaction response. WGCNA further identified tissue-associated co-expression modules enriched in membrane trafficking, phosphatidylinositol signaling, endocytosis, SNARE-mediated vesicular transport, and ubiquitin-mediated protein turnover. Reported GSI-related homologs, including LcS - RNase , LcHT - B , Lc120K , LcStEP , LcSBP1 , and LcSKP1 , also displayed distinct spatiotemporal expression patterns. Integrating these observations, we propose a working model in which heteroall

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