Evidence map›Paper›PMID 16470382›Full record

ArticleMolecular genetics and genomics : MGG2006

Characterization of a novel prospero-related homeobox gene, Prox2.

Ichiko Nishijima, Akihira Ohtoshi

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Molecular genetics and genomics : MGG, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

7 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. 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

2 authors at 1 institution in 1 country.

Ichiko NishijimaCenter of Molecular and Human Genetics, Children's Research Institute, 700 Children's Drive, Columbus, OH 43205, USA.
Akihira Ohtoshi
Children’s Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prospero-related homeobox genes have been identified from various multi-cellular organisms and play important roles in development as a cell fate determinant. Mouse Prox1 is essential for embryogenesis and is required to differentiate horizontal cells in the retina. Here we describe a novel prospero family member, Prox2. Transcriptional reporter assays demonstrated that mouse Prox2 is a transcriptional activator and the N-terminal region has been identified as an activation domain. The expression of mouse Prox2 was detected in postnatal eyes and adult testes as well as embryos. To investigate the in vivo role of Prox2, we generated the Prox2 mutant allele, Prox2-, by homologous recombination in mouse ES cells. Prox2- lacks the first coding exon that encodes a translational start site and a part of homeodomain. In spite of the Prox2 expression during embryogenesis, Prox2- homozygous mutant mice were born at the expected Mendelian ratio without overt abnormalities. Histological analyses revealed that Prox2- homozygous eyes retained the organized layer structure including three nuclear layers and differentiated horizontal cells. Prox2- homozygous mutant males produced elongated spermatids and were fertile. These results demonstrate that mouse Prox2 is dispensable for embryonic development, horizontal cell generation and fertility in contrast to mouse Prox1.

Indexed as

Genes, HomeoboxAnimalsCell DifferentiationCells, CulturedDrosophila ProteinsFemaleFertilityFetal DevelopmentHomeodomain ProteinsMaleMiceMice, Inbred C57BLNerve Tissue ProteinsNuclear ProteinsProspero-Related Homeobox 1 ProteinTranscription FactorsDrosophila ProteinsHomeodomain ProteinsNerve Tissue ProteinsNuclear ProteinsProspero-Related Homeobox 1 Proteinpros protein, DrosophilaTranscription FactorsTumor Suppressor Proteins

Identifiers

PMID16470382
OpenAlexW2081185600

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.