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A multi-cell model for the C4 photosynthetic pathway in developing wheat grains based upon tissue-specific transcriptome data
被引:0
|作者:
Rangan, Parimalan
[1
,2
]
Furtado, Agnelo
[2
]
Chinnusamy, Viswanathan
[3
]
Henry, Robert
[2
]
机构:
[1] ICAR Natl Bur Plant Genet Resources, PUSA Campus, New Delhi 110012, India
[2] Univ Queensland, Queensland Alliance Agr & Food Innovat QAAFI, Brisbane, Qld 4072, Australia
[3] ICAR Indian Agr Res Inst, PUSA Campus, New Delhi 110012, India
来源:
关键词:
NAD-MEC4;
photosynthesis;
C4;
evolution;
Kranz anatomy;
Non-foliar photosynthesis;
BOP clade;
Tissue-specific expression;
Refixation;
ORTHO-PHOSPHATE DIKINASE;
ENZYME-ACTIVITIES;
KRANZ ANATOMY;
EXPRESSION;
PYRUVATE;
PERICARP;
GENE;
LEAF;
OXALOACETATE;
MITOCHONDRIA;
D O I:
10.1016/j.biosystems.2024.105195
中图分类号:
Q [生物科学];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
A non -Kranz C 4 photosynthesis of the NAD-ME subtype, specifically in developing wheat grains (14 dpa, days post-anthesis) was originally demonstrated using transcriptome-based RNA-seq. Here we present a reexamination of evidence for C 4 photosynthesis in the developing grains of wheat and, more broadly, the Pooideae and an investigation of the evolutionary processes and implications. The expression profiles for the genes associated with C 4 photosynthesis (C 4 - and C 3 -specific) were evaluated using published transcriptome data for the outer pericarp, inner pericarp, and endosperm tissues of the developing wheat grains. The expression of the C 4 -specific genes across these three tissues revealed the involvement of all three tissues in an orderly fashion to accomplish the non -Kranz NAD-ME-dependent C 4 photosynthesis. Based on their expression levels in RPKM (reads per kilobase per million mapped reads) values, a model involving multiple cell- and tissue -types is proposed for C 4 photosynthesis involved in the refixation of the respired CO 2 from the endosperm tissues in the developing wheat grains. This multi -cell C 4 model, proposed to involve more than two cell types, requires further biochemical validation.
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