Evidence map›Paper›PMID 8016123›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1994

par-2, a gene required for blastomere asymmetry in Caenorhabditis elegans, encodes zinc-finger and ATP-binding motifs.

D J Levitan, L Boyd, C C Mello, K J Kemphues, D T Stinchcomb

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
0.7field-weighted citation impact, top 27% 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

22 citing papers in PubMed, 87 citations in OpenAlex.

  1. Article
  2. Mechanochemical Control of Symmetry Breaking in theFrontiers in cell and developmental biology · 2020
    Review
  3. Article
  4. Article
  5. Influence of cell polarity on early development of the sea urchin embryo.Developmental dynamics : an official publication of the American Association of Anatomists · 2015
    Article
  6. Article
  7. Article
  8. Signaling pathways in cell polarity.Cold Spring Harbor perspectives in biology · 2012
    Article
  9. Article
  10. Article
  11. Par proteins and neuronal polarity.Developmental neurobiology · 2011
    Review
  12. Article
  13. Article
  14. Widely conserved signaling pathways in the establishment of cell polarity.Cold Spring Harbor perspectives in biology · 2009
    Review
  15. Review
  16. Article
  17. 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

5 authors at 1 institution in 1 country.

D J LevitanDepartment of Cellular and Developmental Biology, Harvard University, Cambridge, MA 02138.
L Boyd
C C Mello
K J Kemphues
D T Stinchcomb
Harvard University · US

Funding

GENETIC ANALYSIS OF EARLY EMBRYOGENESIS IN C ELEGANSR01HD027689 · NICHD · CORNELL UNIVERSITY ITHACA · PI KEMPHUES, KENNETH J. · 1991 to 2005
$2.4M
MOLECULAR GENETICS OF EMBRYOGENESIS IN C. ELEGANSR01HD019039 · NICHD · HARVARD UNIVERSITY · PI STINCHCOMB, DAN THOMAS · 1985 to 1986
–
NICHD NIH HHS HD19039NICHD NIH HHS HD27689
6 · The paper itself

Abstract

The par-2 gene of Caenorhabditis elegans functions in early embryogenesis to ensure an asymmetric first cleavage and the segregation of cytoplasmic factors. Both processes appear to be required to generate daughter blastomeres with distinct developmental potential. We isolated an allele of par-2 by using a screen for maternal-effect lethal mutations in a strain known for its high frequency of transposition events. A transposable element was found to be linked to this allele. Sequences flanking the site of transposon insertion were cloned and found to rescue the par-2 mutant phenotype. DNA in the par-2 region hybridized to a 2.3-kb germ-line-enriched mRNA. The cDNA corresponding to this germ-line-enriched message was cloned, sequenced, and used to identify the molecular lesions associated with three par-2 alleles. Sequence analysis of the par-2 cDNA revealed that the predicted protein contained two distinct motifs found in other known proteins: an ATP-binding site and a cysteine-rich motif which identifies the par-2 gene product as a member of a growing class of putative zinc-binding proteins.

Indexed as

Caenorhabditis elegans ProteinsAdenosine TriphosphateAllelesAmino Acid SequenceAnimalsBase SequenceBinding SitesBlastomeresBlotting, NorthernBlotting, SouthernCaenorhabditis elegansChromosomes, Artificial, YeastCloning, MolecularConsensus SequenceDNADNA PrimersAdenosine TriphosphateCaenorhabditis elegans ProteinsDNADNA PrimersHelminth Proteinspar-2 protein, C elegansRNA, Messenger

Identifiers

PMID8016123
PMCPMC44147
OpenAlexW2055420305

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.