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转录组分析表明,茶树(Camellia sinensis)的自交不亲和性可能受配子体控制。

Transcriptome analysis reveals self-incompatibility in the tea plant (Camellia sinensis) might be under gametophytic control.

作者信息

Zhang Cheng-Cai, Wang Li-Yuan, Wei Kang, Wu Li-Yun, Li Hai-Lin, Zhang Fen, Cheng Hao, Ni De-Jiang

机构信息

Key Laboratory of Tea Biology and Resources Utilization, Ministry of Agriculture, Tea Research Institute Chinese Academy of Agricultural Sciences, 9 Meiling South Road, Hangzhou, 310008, China.

College of Horticulture and Forestry Science, Huazhong Agricultural University, No.1, Shizishan Street, Hongshan District, Wuhan, Hubei Province, 430070, China.

出版信息

BMC Genomics. 2016 May 17;17:359. doi: 10.1186/s12864-016-2703-5.

Abstract

BACKGROUND

Self-incompatibility (SI) is under genetic control and prevents inbreeding depression in angiosperms. SI mechanisms are quite complicated and still poorly understood in many plants. Tea (Camellia sinensis L.) belonging to the family of Theaceae, exhibits high levels of SI and high heterozygosity. Uncovering the molecular basis of SI of the tea plant may enhance breeding and simplify genomics research for the whole family.

RESULTS

The growth of pollen tubes following selfing and crossing was observed using fluorescence microscopy. Self-pollen tubes grew slower than cross treatments from 24 h to 72 h after pollination. RNA-seq was employed to explore the molecular mechanisms of SI and to identify SI-related genes in C. sinensis. Self and cross-pollinated styles were collected at 24 h, 48 h and 72 h after pollination. Six RNA-seq libraries (SP24, SP48, SP72, CP24 CP48 and CP72; SP = self-pollinated, CP = cross-pollinated) were constructed and separately sequenced. In total, 299.327 million raw reads were generated. Following assembly, 63,762 unigenes were identified, and 27,264 (42.76 %) unigenes were annotated in five public databases: NR, KOG, KEGG, Swiss-Port and GO. To identify SI-related genes, the fragments per kb per million mapped reads (FPKM) values of each unigene were evaluated. Comparisons of CP24 vs. SP24, CP48 vs. SP48 and CP72 vs. SP72 revealed differential expression of 3,182, 3,575 and 3,709 genes, respectively. Consequently, several ubiquitin-mediated proteolysis, Ca(2+) signaling, apoptosis and defense-associated genes were obtained. The temporal expression pattern of genes following CP and SP was analyzed; 6 peroxidase, 1 polyphenol oxidase and 7 salicylic acid biosynthetic process-related genes were identified. The RNA-seq data were validated by qRT-PCR of 15 unigenes. Finally, a unigene (CL25983Contig1) with strong homology to the S-RNase was analyzed. It was mainly expressed in styles, with dramatically higher expression in self-pollinated versus cross-pollinated tissues at 24 h post-pollination.

CONCLUSIONS

The present study reports the transcriptome of styles after cross- and self-pollination in tea and offers novel insights into the molecular mechanism behind SI in C. sinensis. We believe that this RNA-seq dataset will be useful for improvement in C. sinensis as well as other plants in the Theaceae family.

摘要

背景

自交不亲和性(SI)受遗传控制,可防止被子植物的近亲繁殖衰退。SI机制相当复杂,在许多植物中仍未得到充分理解。茶树(Camellia sinensis L.)属于山茶科,表现出高度的自交不亲和性和高杂合性。揭示茶树自交不亲和性的分子基础可能会促进育种,并简化整个山茶科的基因组学研究。

结果

使用荧光显微镜观察了自交和杂交后花粉管的生长情况。授粉后24小时至72小时,自花花粉管的生长速度比杂交处理的花粉管慢。采用RNA测序技术探索茶树自交不亲和性的分子机制,并鉴定与自交不亲和性相关的基因。在授粉后24小时、48小时和72小时收集自花授粉和异花授粉的花柱。构建了六个RNA测序文库(SP24、SP48、SP72、CP24、CP48和CP72;SP = 自花授粉,CP = 异花授粉)并分别进行测序。总共产生了2.99327亿条原始读数。组装后,鉴定出63762个单基因,其中27264个(42.76%)单基因在五个公共数据库(NR、KOG、KEGG、Swiss-Port和GO)中得到注释。为了鉴定与自交不亲和性相关的基因,评估了每个单基因的每百万映射读数中每千碱基的片段数(FPKM)值。CP24与SP24、CP48与SP48以及CP72与SP72的比较分别揭示了3182、3575和3709个基因的差异表达。因此,获得了几个泛素介导的蛋白水解、Ca(2+)信号传导、细胞凋亡和防御相关基因。分析了CP和SP后基因的时间表达模式;鉴定出6个过氧化物酶、1个多酚氧化酶和7个水杨酸生物合成过程相关基因。通过对15个单基因的qRT-PCR验证了RNA测序数据。最后,分析了一个与S-RNase具有高度同源性的单基因(CL25983Contig1)。它主要在花柱中表达,在授粉后24小时,自花授粉组织中的表达明显高于异花授粉组织。

结论

本研究报告了茶树异花授粉和自花授粉后花柱的转录组,并为茶树自交不亲和性背后的分子机制提供了新的见解。我们相信,这个RNA测序数据集将有助于茶树以及山茶科其他植物的改良。

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