Evidence map›Paper›PMID 30199528›Full record

ArticlePloS one2018

Propagation of cell death in dropdead1, a sorghum ortholog of the maize lls1 mutant.

Anoop Sindhu, Diane Janick-Buckner, Brent Buckner, John Gray, Usha Zehr, Brian P Dilkes, Gurmukh S Johal

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 34% of its field
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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Singlet Oxygen Generation and Signaling in Higher Plants.International journal of molecular sciences · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. International journal of molecular sciences · 2019
    Article
  6. AG3 (Bethesda, Md.) · 2019
    Article
  7. 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

7 authors at 3 institutions in 1 country.

Anoop SindhuDepartment of Botany and Plant Pathology, Purdue University, West Lafayette, Indiana, United States of America.
Diane Janick-BucknerDepartment of Biology, Truman State University, Kirksville, Missouri, United States of America.
Brent BucknerDepartment of Biology, Truman State University, Kirksville, Missouri, United States of America.
John GrayBiological Sciences Department, University of Toledo, Toledo, Ohio, United States of America.
Usha ZehrDepartment of Agronomy, Purdue University, West Lafayette, Indiana, United States of America.
Brian P DilkesDepartment of Biochemistry, Purdue University, West Lafayette, Indiana, United States of America.ORCID 0000-0003-2799-954X
Gurmukh S JohalDepartment of Botany and Plant Pathology, Purdue University, West Lafayette, Indiana, United States of America.
Purdue University West Lafayette · USTruman State University · USUniversity of Toledo · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We describe dropdead1-1 (ded1), an EMS-induced recessive lesion mimic mutant of sorghum. It is characterized by the formation of spreading necrotic lesions that share many attributes with those associated with the maize lethal leaf spot1 (lls1) and Arabidopsis accelerated cell death1 (acd1) mutation. We show that as in lls1, ded1 lesions are initiated by wounding and require light for continued propagation, and that loss of chloroplast integrity is responsible for ded1 cell death. Consistent with these parallels, we demonstrate that ded1 is an ortholog of lls1 and encodes pheophorbide a oxidase (PaO) with 93% identity at the protein level. The mutant ded1 allele resulted from a stop codon-inducing single base pair change in exon 6 of the sorghum ortholog of lls1. The ded1 transcript was rapidly and transiently induced after wounding and substantially elevated in leaves containing ded1 lesions. Given that PaO is a key enzyme of the chlorophyll degradation pathway, its dysfunction would result in the accumulation of pheophorbide, a potent photosensitizer that results in the production of singlet oxygen. Consistent with this, cell death associated with ded1 lesions is most likely caused by singlet oxygen as our results exclude superoxide and H2O2 from this role. We explore the signal responsible for the propagation of lesions affecting both ded1 and lls1 lesions and find that both developmental age and ethylene increase the rate of lesion expansion in both mutants.

Indexed as

MutationPlant ProteinsSorghumApoptosis Regulatory ProteinsCell DeathChlorophyllHydrogen PeroxideOxidoreductasesSuperoxidesZea maysApoptosis Regulatory ProteinsChlorophyllHydrogen PeroxideOxidoreductasesPlant ProteinsSuperoxides

Identifiers

PMID30199528
PMCPMC6130852
OpenAlexW2890447071

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.