Evidence map›Paper›PMID 10938131›Full record

ArticleMolecular and cellular biology2000

Divergent N-terminal sequences target an inducible testis deubiquitinating enzyme to distinct subcellular structures.

H Lin, A Keriel, C R Morales, N Bedard, Q Zhao, P Hingamp, S Lefrançois, L Combaret, S S Wing

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 20% 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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 73 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. USP2-Related Cellular Signaling and Consequent Pathophysiological Outcomes.International journal of molecular sciences · 2021
    Review
  9. Article
  10. Article
  11. Article
  12. The role of deubiquitinating enzymes in spermatogenesis.Cellular and molecular life sciences : CMLS · 2015
    Review
  13. Deubiquitinases in skeletal muscle atrophy.The international journal of biochemistry & cell biology · 2013
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. The role of deubiquitinating enzymes in apoptosis.Cellular and molecular life sciences : CMLS · 2011
    Review
  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

9 authors at 1 institution in 1 country.

H LinDepartment of Medicine, McGill University, Montreal, Canada.
A Keriel
C R Morales
N Bedard
Q Zhao
P Hingamp
S Lefrançois
L Combaret
S S Wing
McGill University · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ubiquitin-specific processing proteases (UBPs) presently form the largest enzyme family in the ubiquitin system, characterized by a core region containing conserved motifs surrounded by divergent sequences, most commonly at the N-terminal end. The functions of these divergent sequences remain unclear. We identified two isoforms of a novel testis-specific UBP, UBP-t1 and UBP-t2, which contain identical core regions but distinct N termini, thereby permitting dissection of the functions of these two regions. Both isoforms were germ cell specific and developmentally regulated. Immunocytochemistry revealed that UBP-t1 was induced in step 16 to 19 spermatids while UBP-t2 was expressed in step 18 to 19 spermatids. Immunoelectron microscopy showed that UBP-t1 was found in the nucleus while UBP-t2 was extranuclear and was found in residual bodies. For the first time, we show that the differential subcellular localization was due to the distinct N-terminal sequences. When transfected into COS-7 cells, the core region was expressed throughout the cell but the UBP-t1 and UBP-t2 isoforms were concentrated in the nucleus and the perinuclear region, respectively. Fusions of each N-terminal end with green fluorescent protein yielded the same subcellular localization as the native proteins, indicating that the N-terminal ends were sufficient for determining differential localization. Interestingly, UBP-t2 colocalized with anti-gamma-tubulin immunoreactivity, indicating that like several other components of the ubiquitin system, a deubiquitinating enzyme is associated with the centrosome. Regulated expression and alternative N termini can confer specificity of UBP function by restricting its temporal and spatial loci of action.

Indexed as

Age FactorsAmino Acid SequenceAnimalsBlotting, NorthernCell NucleusCentrosomeCOS CellsDNA, ComplementaryEndopeptidasesGreen Fluorescent ProteinsImmunohistochemistryIsoenzymesLuminescent ProteinsMaleMicroscopy, ImmunoelectronMolecular Sequence DataDNA, ComplementaryEndopeptidasesGreen Fluorescent ProteinsIsoenzymesLuminescent ProteinsMuscle ProteinsRecombinant Fusion ProteinsRNA, MessengerUbiquitin ThiolesteraseUsp2 protein, rat

Identifiers

PMID10938131
PMCPMC86134
OpenAlexW2113866575

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.