Evidence map›Paper›PMID 19706172›Full record

ArticleBMC genomics2009

Implications of high level pseudogene transcription in Mycobacterium leprae.

Diana L Williams, Richard A Slayden, Amol Amin, Alejandra N Martinez, Tana L Pittman, Alex Mira, Anirban Mitra, Valakunja Nagaraja, Norman E Morrison, Milton Moraes and 1 more

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

26 citing papers in PubMed, 48 citations in OpenAlex.

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  7. Adhesive Functions or Pseudogenization of Type Va Autotransporters inFrontiers in cellular and infection microbiology · 2021
    Article
  8. Frontiers in cellular and infection microbiology · 2021
    Article
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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

11 authors at 6 institutions in 3 countries.

Diana L WilliamsHRSA, BPHC, Division of National Hansen's Disease Programs, Laboratory Research Branch, Molecular Biology Research Department, School of Veterinary Medicine, Louisiana State University, Baton Rouge, LA, USA. dwill21@lsu.edu
Richard A Slayden
Amol Amin
Alejandra N Martinez
Tana L Pittman
Alex Mira
Anirban Mitra
Valakunja Nagaraja
Norman E Morrison
Milton Moraes
Thomas P Gillis
Louisiana State University · USColorado State University · USIndian Institute of Science Bangalore · INFundação Oswaldo Cruz · BRJohns Hopkins University · USNational Hansen's Disease Program · US

Funding

Regulation of Cellular division in M. tuberculosisR01AI055298 · NIAID · COLORADO STATE UNIVERSITY-FORT COLLINS · PI SLAYDEN, RICHARD A · 2003 to 2006
$915k
Leprosy Research Support-Post Genome -26625469N01AI025469 · NIAID · Colorado State University · 2004 to 2004
–
NIAID NIH HHS AI-55298NIAID NIH HHS N01 AI025469NIAID NIH HHS N01 AI040091NIAID NIH HHS N01 AI-25469NIAID NIH HHS N01 AI-40091NIAID NIH HHS R01 AI055298NIAID NIH HHS YI-AI-2646-01
6 · The paper itself

Abstract

backgroundThe Mycobacterium leprae genome has less than 50% coding capacity and 1,133 pseudogenes. Preliminary evidence suggests that some pseudogenes are expressed. Therefore, defining pseudogene transcriptional and translational potentials of this genome should increase our understanding of their impact on M. leprae physiology.

resultsGene expression analysis identified transcripts from 49% of all M. leprae genes including 57% of all ORFs and 43% of all pseudogenes in the genome. Transcribed pseudogenes were randomly distributed throughout the chromosome. Factors resulting in pseudogene transcription included: 1) co-orientation of transcribed pseudogenes with transcribed ORFs within or exclusive of operon-like structures; 2) the paucity of intrinsic stem-loop transcriptional terminators between transcribed ORFs and downstream pseudogenes; and 3) predicted pseudogene promoters. Mechanisms for translational "silencing" of pseudogene transcripts included the lack of both translational start codons and strong Shine-Dalgarno (SD) sequences. Transcribed pseudogenes also contained multiple "in-frame" stop codons and high Ka/Ks ratios, compared to that of homologs in M. tuberculosis and ORFs in M. leprae. A pseudogene transcript containing an active promoter, strong SD site, a start codon, but containing two in frame stop codons yielded a protein product when expressed in E. coli.

conclusionApproximately half of M. leprae's transcriptome consists of inactive gene products consuming energy and resources without potential benefit to M. leprae. Presently it is unclear what additional detrimental affect(s) this large number of inactive mRNAs has on the functional capability of this organism. Translation of these pseudogenes may play an important role in overall energy consumption and resultant pathophysiological characteristics of M. leprae. However, this study also demonstrated that multiple translational "silencing" mechanisms are present, reducing additional energy and resource expenditure required for protein production from the vast majority of these transcripts.

Indexed as

Gene Expression ProfilingGenome, BacterialPseudogenesBase SequenceCodon, InitiatorCodon, TerminatorGene Expression Regulation, BacterialGenes, BacterialGene SilencingMolecular Sequence DataMycobacterium lepraeOligonucleotide Array Sequence AnalysisOpen Reading FramesPromoter Regions, GeneticProtein BiosynthesisTranscription, GeneticCodon, InitiatorCodon, Terminator

Identifiers

PMID19706172
PMCPMC2753549
OpenAlexW2092233856

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.