Evidence map›Paper›PMID 39688921›Full record

ArticleAnnals of botany2025

Evolutionary diversification of C2 photosynthesis in the grass genus Homolepis (Arthropogoninae).

Joyce Pereira Alvarenga, Matt Stata, Rowan F Sage, Ria Patel, Ane Marcela das Chagas Mendonca, Felipe Della Torre, Hongbing Liu, Shifeng Cheng, Samantha Weake, Emile J Watanabe and 5 more

Abstract read
In one paragraph

Article in Annals of botany, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. CBiology · 2025
    Review
  3. Article
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Joyce Pereira AlvarengaLaboratory of Ecophysiology, Plant Physiology Sector, Department of Biology, Federal University of Lavras, Lavras, Minas Gerais, 37200-900, Brazil.
Matt StataDepartment of Ecology and Evolutionary Biology, University of Toronto, Ontario, M5S 3B2, Canada.
Rowan F SageDepartment of Ecology and Evolutionary Biology, University of Toronto, Ontario, M5S 3B2, Canada.
Ria PatelDepartment of Ecology and Evolutionary Biology, University of Toronto, Ontario, M5S 3B2, Canada.
Ane Marcela das Chagas MendoncaLaboratory of Ecophysiology, Plant Physiology Sector, Department of Biology, Federal University of Lavras, Lavras, Minas Gerais, 37200-900, Brazil.
Felipe Della TorreDepartment of Ecology and Evolutionary Biology, University of Toronto, Ontario, M5S 3B2, Canada.
Hongbing LiuShenzhen Branch, Guangdong Laboratory for Lingnan Modern Agriculture, Genome Analysis Laboratory of the Ministry of Agriculture, Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen, 518120, China.
Shifeng ChengShenzhen Branch, Guangdong Laboratory for Lingnan Modern Agriculture, Genome Analysis Laboratory of the Ministry of Agriculture, Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen, 518120, China.
Samantha WeakeDepartment of Ecology and Evolutionary Biology, University of Toronto, Ontario, M5S 3B2, Canada.
Emile J WatanabeDepartment of Ecology and Evolutionary Biology, University of Toronto, Ontario, M5S 3B2, Canada.
Pedro Lage VianaInstituto Nacional da Mata Atlantica, Santa Teresa, Espirito Santo, 29650-000, Brazil.
Iago Augusto de Castro ArrudaLaboratory of Ecophysiology, Plant Physiology Sector, Department of Biology, Federal University of Lavras, Lavras, Minas Gerais, 37200-900, Brazil.
Martha LudwigSchool of Molecular Sciences, University of Western Australia, Crawley, WA 6009, Australia.
João Paulo Rodrigues Alves Delfino BarbosaLaboratory of Ecophysiology, Plant Physiology Sector, Department of Biology, Federal University of Lavras, Lavras, Minas Gerais, 37200-900, Brazil.
Tammy L SageDepartment of Ecology and Evolutionary Biology, University of Toronto, Ontario, M5S 3B2, Canada.

Funding

Fundação de Amparo à Pesquisa do Estado de Minas Gerais, Brazil (FAPEMIG) project APQ-02653-18Natural Science and Engineering Research Council of Canada RGPIN-2020-05925
6 · The paper itself

Abstract

BACKGROUND AND

aimsTo better understand C4 evolution in monocots, we characterized C3-C4 intermediate phenotypes in the grass genus Homolepis (subtribe Arthropogoninae).

methodsCarbon isotope ratio (δ13C), leaf gas exchange, mesophyll (M) and bundle sheath (BS) tissue characteristics, organelle size and numbers in M and BS tissue, and tissue distribution of the P-subunit of glycine decarboxylase (GLDP) were determined for five Homolepis species and the C4 grass Mesosetum loliiforme from a phylogenetic sister clade. We generated a transcriptome-based phylogeny for Homolepis and Mesosetum species to interpret physiological and anatomical patterns in an evolutionary context, and to test for hybridization. KEY

resultsHomolepis contains two C3 species (H. glutinosa, H. villaricensis), one species with a weaker form of C2 termed sub-C2 (H. isocalycia), and two C2 species (H. longispicula, H. aturensis). Homolepis longispicula and H. aturensis express over 85 % of leaf glycine in centripetal mitochondria within the BS, and have increased fractions of leaf chloroplasts, mitochondria and peroxisomes within the BS relative to H. glutinosa. Analysis of leaf gas exchange, cell ultrastructure and transcript expression show M. loliiforme is a C4 plant of the NADP-malic enzyme subtype. Homolepis comprises two sister clades, one containing H. glutinosa and H. villaricensis and the second H. longispicula and H. aturensis. Homolepis isocalycia is of hybrid origin, its parents being H. aturensis and a common ancestor of the C3  Homolepis clade and H. longispicula.

conclusionsPhotosynthetic activation of BS tissue in the sub-C2 and C2 species of Homolepis is similar to patterns observed in C3-C4 intermediate eudicots, indicating common evolutionary pathways from C3 to C4 photosynthesis in these disparate clades. Hybridization can diversify the C3-C4 intermediate character state and should be considered in reconstructing putative ancestral states using phylogenetic analyses.

Indexed as

Biological EvolutionPhotosynthesisPoaceaeCarbon IsotopesGlycine Dehydrogenase (Decarboxylating)PhylogenyPlant LeavesPlant ProteinsTranscriptomeCarbon IsotopesGlycine Dehydrogenase (Decarboxylating)Plant ProteinsC2 photosynthesisC3–C4 intermediateC4 photosynthesisCarbon concentrating mechanismglycine decarboxylaseleaf anatomyphotosynthetic evolution

Identifiers

PMID39688921
PMCPMC11904902

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