Paper · 2003 · The Plant Cell

Unique Architecture of the Plastid Ribosomal RNA Operon Promoter Recognized by the Multisubunit RNA Polymerase in Tobacco and Other Higher Plants

Jon Y. Suzuki; Priya Sriraman; Zora Svab; et al.

5
claims
10
verbatim quotes
63
citations
1
research areas
✓
Open access

Abstract

Expression of the plastid rRNA operon (rrn) during development is highly regulated at the level of transcription. The plastid rrn operon in most higher plants is transcribed by the plastid-encoded RNA polymerase (PEP), the multisubunit plastid RNA polymerase from PrrnP1, a sigma(70)-type promoter with conserved -10 and -35 core promoter elements. To identify functionally important sequences, the tobacco PrrnP1 was dissected in vivo and in vitro. Based on in vivo deletion analysis, sequences upstream of nucleotide -83 do not significantly contribute to promoter function. The in vitro analyses identified an essential hexameric sequence upstream of the -35 element (GTGGGA; the rRNA operon upstream activator [RUA]) that is conserved in monocot and dicot species and suggested that the -10 element plays only a limited role in PrrnP1 recognition. Mutations in the initial transcribed sequence (+9 to +14) enhanced transcription, the characteristic of strong promoters in prokaryotes. We propose that sigma interaction with the -10 element in PrrnP1 is replaced in part by direct PEP-RUA (protein-DNA) interaction or by protein-protein interaction between the PEP and an RUA binding transcription factor.

Abstract from the paper’s OpenAlex record, shown for indexing and research. Copyright remains with the authors or the publisher. Read at the source ↗

The text the model read, with the source record’s inline markup (italics, sub- and superscripts) rendered and its character entities decoded; quote offsets refer to the raw text.

Claims 5

Observationobservedoriginal resultnot significant (as stated)measured

Claim · model-written summary

Sequences upstream of -83 did not significantly contribute to promoter function.

Gene
promotere0
Outcome
promoter functione0
Direction
do not significantly contributee0

Organisms pictured · Representative pictures of the matched species, not figures from the paper.

Nicotiana tabacum
Nicotiana tabacum · TaxonJom / Joachim Müllerchen · CC BY 2.5 · Wikimedia Commons ↗

Verbatim

e0

“Based on in vivo deletion analysis, sequences upstream of nucleotide -83 do not significantly contribute to promoter function.”

✓ located verbatim in the source · abstract, characters 450–576 · show in text ↑
t0

“Tobacco”

✓ located verbatim in the source · title, characters 114–121 · show in text ↑
Observationobservedoriginal resultmeasured

Claim · model-written summary

An essential upstream hexameric RUA sequence was identified and conserved across monocots and dicots.

Gene
rRNA operon upstream activator [RUA]e0
Outcome
essential hexameric sequencee0
Value
GTGGGAe0
Qualifier
conserved in monocot and dicot speciese0

Organisms pictured · Representative pictures of the matched species, not figures from the paper.

Nicotiana tabacum
Nicotiana tabacum · TaxonJom / Joachim Müllerchen · CC BY 2.5 · Wikimedia Commons ↗

Verbatim

e0

“The in vitro analyses identified an essential hexameric sequence upstream of the -35 element (GTGGGA; the rRNA operon upstream activator [RUA]) that is conserved in monocot and dicot species and suggested that the -10 element plays only a limited role in PrrnP1 recognition.”

✓ located verbatim in the source · abstract, characters 577–851 · show in text ↑
t0

“Tobacco”

✓ located verbatim in the source · title, characters 114–121 · show in text ↑
Observationauthor interpretationoriginal resultmeasured

Claim · model-written summary

The -10 element played only a limited role in PrrnP1 recognition.

Gene
PrrnP1e0
Outcome
limited role in PrrnP1 recognitione0

Organisms pictured · Representative pictures of the matched species, not figures from the paper.

Nicotiana tabacum
Nicotiana tabacum · TaxonJom / Joachim Müllerchen · CC BY 2.5 · Wikimedia Commons ↗

Verbatim

e0

“The in vitro analyses identified an essential hexameric sequence upstream of the -35 element (GTGGGA; the rRNA operon upstream activator [RUA]) that is conserved in monocot and dicot species and suggested that the -10 element plays only a limited role in PrrnP1 recognition.”

✓ located verbatim in the source · abstract, characters 577–851 · show in text ↑
t0

“Tobacco”

✓ located verbatim in the source · title, characters 114–121 · show in text ↑
Intervention effectobservedoriginal resultpositivemeasured

Claim · model-written summary

Mutations at +9 to +14 enhanced transcription.

Treatment
Mutations in the initial transcribed sequence (+9 to +14)e0
Outcome
transcriptione0
Direction
enhancede0

Not reportedComparator

Organisms pictured · Representative pictures of the matched species, not figures from the paper.

Nicotiana tabacum
Nicotiana tabacum · TaxonJom / Joachim Müllerchen · CC BY 2.5 · Wikimedia Commons ↗

Verbatim

e0

“Mutations in the initial transcribed sequence (+9 to +14) enhanced transcription, the characteristic of strong promoters in prokaryotes.”

✓ located verbatim in the source · abstract, characters 852–988 · show in text ↑
t0

“Tobacco”

✓ located verbatim in the source · title, characters 114–121 · show in text ↑
Mechanismhypothesisoriginal resultbasis n/a

Claim · model-written summary

The authors propose PEP-RUA or PEP-factor interactions partly replace sigma interaction with the -10 element.

Gene
PrrnP1e0
Outcome
sigma interaction with the -10 element in PrrnP1e0
Qualifier
direct PEP-RUA (protein-DNA) interaction or by protein-protein interaction between the PEP and an RUA binding transcription factore0

Organisms pictured · Representative pictures of the matched species, not figures from the paper.

Nicotiana tabacum
Nicotiana tabacum · TaxonJom / Joachim Müllerchen · CC BY 2.5 · Wikimedia Commons ↗

Verbatim

e0

“We propose that sigma interaction with the -10 element in PrrnP1 is replaced in part by direct PEP-RUA (protein-DNA) interaction or by protein-protein interaction between the PEP and an RUA binding transcription factor.”

✓ located verbatim in the source · abstract, characters 989–1208 · show in text ↑
t0

“Tobacco”

✓ located verbatim in the source · title, characters 114–121 · show in text ↑

loss of function · molecular: expression · Nicotiana tabacum (tobacco)Positive and negative results

50 papers: 14 positive, 36 negative or no effect

13 papers in the same direction as this paper · 36 in the opposite direction

  1. negative
  2. negative
  3. negative

46 papers more in this group

See all 50 papers →

Claims are grouped by organism, treatment and what was measured or targeted. A paper counts as positive when any of its claims in the group is positive.