High-Resolution Profiling of a Synchronized Diurnal Transcriptome from Chlamydomonas reinhardtii Reveals Continuous Cell and Metabolic Differentiation

被引:194
作者
Zones, James Matt [1 ,2 ]
Blaby, Ian K. [3 ]
Merchant, Sabeeha S. [3 ,4 ]
Umen, James G. [1 ]
机构
[1] Donald Danforth Plant Sci Ctr, St Louis, MO 63132 USA
[2] Univ Calif San Diego, Div Biol Sci, La Jolla, CA 92093 USA
[3] Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
[4] Univ Calif Los Angeles, Inst Genom & Prote, Los Angeles, CA 90095 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
LIGHT-REPRESSED TRANSCRIPT; CIRCADIAN CLOCK; GENE-EXPRESSION; CHLOROPLAST DIVISION; RIBOSOMAL-PROTEIN; CO2-CONCENTRATING MECHANISM; BALANCED PRODUCTION; PROTEOMIC ANALYSIS; PLASTID DIVISION; GENOMIC ANALYSIS;
D O I
10.1105/tpc.15.00498
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The green alga Chlamydomonas reinhardtii is a useful model organism for investigating diverse biological processes, such as photosynthesis and chloroplast biogenesis, flagella and basal body structure/function, cell growth and division, and many others. We combined a highly synchronous photobioreactor culture system with frequent temporal sampling to characterize genome-wide diurnal gene expression in Chlamydomonas. Over 80% of the measured transcriptome was expressed with strong periodicity, forming 18 major clusters. Genes associated with complex structures and processes, including cell cycle control, flagella and basal bodies, ribosome biogenesis, and energy metabolism, all had distinct signatures of coexpression with strong predictive value for assigning and temporally ordering function. Importantly, the frequent sampling regime allowed us to discern meaningful fine-scale phase differences between and within subgroups of genes and enabled the identification of a transiently expressed cluster of light stress genes. Coexpression was further used both as a data-mining tool to classify and/or validate genes from other data sets related to the cell cycle and to flagella and basal bodies and to assign isoforms of duplicated enzymes to their cognate pathways of central carbon metabolism. Our diurnal coexpression data capture functional relationships established by dozens of prior studies and are a valuable new resource for investigating a variety of biological processes in Chlamydomonas and other eukaryotes.
引用
收藏
页码:2743 / 2769
页数:27
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