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1.
BMC Plant Biol ; 20(1): 508, 2020 Nov 05.
Article in English | MEDLINE | ID: mdl-33153428

ABSTRACT

BACKGROUND: Cunninghamia lanceolata (Chinese fir), a member of the conifer family Cupressaceae, is one of the most popular cultivated trees for wood production in China. Continuous research is being performed to improve C. lanceolata breeding values. Given the high rate of seed abortion (one of the reasons being the failure of ovule and pollen development) in C. lanceolata, the proper formation of female/male cones could theoretically increase the number of offspring in future generations. MIKC MADS-box genes are well-known for their roles in the flower/cone development and comprise the typical/atypical floral development model for both angiosperms and gymnosperms. RESULTS: We performed a transcriptomic analysis to find genes differentially expressed between female and male cones at a single, carefully determined developmental stage, focusing on the MIKC MADS-box genes. We finally obtained 47 unique MIKC MADS-box genes from C. lanceolata and divided these genes into separate branches. 27 out of the 47 MIKC MADS-box genes showed differential expression between female and male cones, and most of them were not expressed in leaves. Out of these 27 genes, most B-class genes (AP3/PI) were up-regulated in the male cone, while TM8 genes were up-regulated in the female cone. Then, with no obvious overall preference for AG (class C + D) genes in female/male cones, it seems likely that these genes are involved in the development of both cones. Finally, a small number of genes such as GGM7, SVP, AGL15, that were specifically expressed in female/male cones, making them candidate genes for sex-specific cone development. CONCLUSIONS: Our study identified a number of MIKC MADS-box genes showing differential expression between female and male cones in C. lanceolata, illustrating a potential link of these genes with C. lanceolata cone development. On the basis of this, we postulated a possible cone development model for C. lanceolata. The gene expression library showing differential expression between female and male cones shown here, can be used to discover unknown regulatory networks related to sex-specific cone development in the future.


Subject(s)
Cunninghamia/genetics , Genes, Plant/physiology , MADS Domain Proteins/physiology , Plant Components, Aerial/growth & development , Transcriptome/genetics , Cunninghamia/growth & development , Cunninghamia/ultrastructure , Gene Expression Profiling , Genes, Plant/genetics , MADS Domain Proteins/genetics , Microscopy, Electron, Scanning , Plant Components, Aerial/metabolism , Plant Components, Aerial/ultrastructure , Real-Time Polymerase Chain Reaction , Transcriptome/physiology
2.
Planta ; 250(1): 163-171, 2019 Jul.
Article in English | MEDLINE | ID: mdl-30953149

ABSTRACT

MAIN CONCLUSION: Glucomannan was more strongly oriented, in line with the orientation of cellulose, than the xylan in both compression wood and normal wood of Chinese fir. Lignin in compression wood was somewhat more oriented in the direction of the cellulose microfibrils than in normal wood. The structural organization in compression wood (CW) is quite different from that in normal wood (NW). To shed more light on the structural organization of the polymers in plant cell walls, Fourier Transform Infrared (FTIR) microscopy in transmission mode has been used to compare the S2-dominated mean orientation of wood polymers in CW with that in NW from Chinese fir (Cunninghamia lanceolata). Polarized FTIR measurements revealed that in both CW and NW samples, glucomannan and xylan showed a parallel orientation with respect to the cellulose microfibrils. In both wood samples, the glucomannan showed a much greater degree of orientation than the xylan, indicating that the glucomannan has established a stronger interaction with cellulose than xylan. For the lignin, the absorption peak also indicated an orientation along the direction of the cellulose microfibrils, but this orientation was more pronounced in CW than in NW, indicating that the lignin is affected by the orientation of the cellulose microfibrils more strongly in CW than it is in NW.


Subject(s)
Cunninghamia/ultrastructure , Polymers/metabolism , Cell Wall/metabolism , Cell Wall/ultrastructure , Cellulose/metabolism , Cunninghamia/metabolism , Lignin/metabolism , Mannans/metabolism , Microfibrils , Spectroscopy, Fourier Transform Infrared , Wood/metabolism , Wood/ultrastructure , Xylans/metabolism
3.
Plant Physiol ; 172(4): 2347-2362, 2016 12.
Article in English | MEDLINE | ID: mdl-27760880

ABSTRACT

Seeds with physiological dormancy usually experience primary and secondary dormancy in the nature; however, little is known about the differential regulation of primary and secondary dormancy. We combined multiple approaches to investigate cytological changes, hormonal levels, and gene expression dynamics in Cunninghamia lanceolata seeds during primary dormancy release and secondary dormancy induction. Light microscopy and transmission electron microscopy revealed that protein bodies in the embryo cells coalesced during primary dormancy release and then separated during secondary dormancy induction. Transcriptomic profiling demonstrated that expression of genes negatively regulating gibberellic acid (GA) sensitivity reduced specifically during primary dormancy release, whereas the expression of genes positively regulating abscisic acid (ABA) biosynthesis increased during secondary dormancy induction. Parallel analysis of RNA ends revealed uncapped transcripts for ∼55% of all unigenes. A negative correlation between fold changes in expression levels of uncapped versus capped mRNAs was observed during primary dormancy release. However, this correlation was loose during secondary dormancy induction. Our analyses suggest that the reversible changes in cytology and gene expression during dormancy release and induction are related to ABA/GA balance. Moreover, mRNA degradation functions as a critical posttranscriptional regulator during primary dormancy release. These findings provide a mechanistic framework for understanding physiological dormancy in seeds.


Subject(s)
Cunninghamia/genetics , Plant Dormancy/genetics , RNA Stability/genetics , Seeds/genetics , Transcriptome/genetics , Abscisic Acid/pharmacology , Cell Wall/drug effects , Cell Wall/metabolism , Cunninghamia/cytology , Cunninghamia/drug effects , Cunninghamia/ultrastructure , Gene Expression Profiling , Gene Expression Regulation, Plant/drug effects , Genes, Plant , Germination/drug effects , Germination/genetics , Gibberellins/pharmacology , MicroRNAs/genetics , MicroRNAs/metabolism , Molecular Sequence Annotation , Plant Dormancy/drug effects , Plant Growth Regulators/pharmacology , RNA Stability/drug effects , RNA, Messenger/genetics , RNA, Messenger/metabolism , Reproducibility of Results , Seeds/cytology , Seeds/drug effects , Seeds/ultrastructure , Sequence Analysis, RNA , Transcriptome/drug effects
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