Evidence map›Paper›PMID 10330475›Full record

ArticleThe Plant cell1999

Functional analysis of two maize cDNAs encoding T7-like RNA polymerases.

C C Chang, J Sheen, M Bligny, Y Niwa, S Lerbs-Mache, D B Stern

Abstract read
In one paragraph

Article in The Plant cell, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing 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

46 citing papers in PubMed.

  1. Article
  2. SlPPR138-mediated RNA editing ofHorticulture research · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. Plastid Gene Transcription: An Update on Promoters and RNA Polymerases.Methods in molecular biology (Clifton, N.J.) · 2021
    Article
  7. Bacteriophages and Bacterial Plant Diseases.Frontiers in microbiology · 2017
    Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Post-transcriptional control of chloroplast gene expression.Gene regulation and systems biology · 2009
    Article
  17. Intraplastidial trafficking of a phage-type RNA polymerase is mediated by a thylakoid RING-H2 protein.Proceedings of the National Academy of Sciences of the United States of America · 2008
    Article
  18. Article
  19. Article
  20. 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

6 authors.

C C ChangBoyce Thompson Institute for Plant Research, Tower Road, Cornell University, Ithaca, New York 14853-1801, USA.
J Sheen
M Bligny
Y Niwa
S Lerbs-Mache
D B Stern

Funding

IN VITRO ANALYSIS OF PLANT MITOCHONDRIAL TRANSCRIPTIONR01GM052560 · NIGMS · BOYCE THOMPSON INST FOR PLANT RESEARCH · PI STERN, DAVID B · 1995 to 1997
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NIGMS NIH HHS R01GM52560
6 · The paper itself

Abstract

We have characterized two maize cDNAs, rpoTm and rpoTp, that encode putative T7-like RNA polymerases. In vivo cellular localization experiments using transient expression of the green fluorescent protein suggest that their encoded proteins are targeted exclusively to mitochondria and plastids, respectively. An antibody raised against the C terminus of the rpoTp gene product identified mitochondrial polypeptides of approximately 100 kD. Their presence was correlated with RNA polymerase activity, and the antibody inhibited mitochondrial in vitro transcription activity. Together, these results strongly suggest that the product of rpoTm is involved in maize mitochondrial transcription. By contrast, immunoblot analysis and an antibody-linked polymerase assay indicated that rpoTp specifies a plastid RNA polymerase component. A quantitative reverse transcription-polymerase chain reaction assay was used to study the transcription of rpoTp and rpoTm in different tissues and under different environmental conditions. Although both genes were constitutively expressed, rpoTm transcripts were generally more prevalent in nonphotosynthetic tissues, whereas an increase in rpoTp transcripts paralleled chloroplast development. We suggest that these two genes encode constitutive components of the organelle transcription machinery but that their expression is nonetheless subject to modulation during plant development.

Indexed as

Amino Acid SequenceCell CompartmentationChloroplastsCloning, MolecularConserved SequenceDNA, ComplementaryDNA-Directed RNA PolymerasesGene DosageGreen Fluorescent ProteinsLuminescent ProteinsMitochondriaMolecular Sequence DataRecombinant Fusion ProteinsRNA, MessengerRNA, PlantSequence Homology, Amino Acidbacteriophage T7 RNA polymeraseDNA, ComplementaryDNA-Directed RNA PolymerasesGreen Fluorescent ProteinsLuminescent ProteinsRecombinant Fusion ProteinsRNA, MessengerRNA, PlantViral Proteins

Identifiers

PMID10330475
PMCPMC144232

What OpenQuestion holds

Textmetadata
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.