ArticleMolecular genetics and genomics : MGG2006
Characterization of a novel prospero-related homeobox gene, Prox2.
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.
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Who cites it
7 citing papers in PubMed, 19 citations in OpenAlex.
- Single cell transcriptomics of the developing zebrafish lens and identification of putative controllers of lens development.Experimental eye research · 2021Article
- Vertebrate Sensory Ganglia: Common and Divergent Features of the Transcriptional Programs Generating Their Functional Specialization.Frontiers in cell and developmental biology · 2020Review
- Identification of molecular signatures specific for distinct cranial sensory ganglia in the developing chick.Neural development · 2016Article
- Prospero-related homeobox 1 (Prox1) functions as a novel modulator of retinoic acid-related orphan receptors α- and γ-mediated transactivation.Nucleic acids research · 2013Article
- Classification and nomenclature of all human homeobox genes.BMC biology · 2007Article
- A brain-specific homeobox gene, Bsx, is essential for proper postnatal growth and nursing.Molecular and cellular biology · 2007Article
- Cloning and functional analysis of hypothalamic homeobox gene Bsx1a and its isoform, Bsx1b.Molecular and cellular biology · 2007Article
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Authors and funding
2 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
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.
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