4.0 Article

Transgenic Analysis of the Physiological Functions of Mahogunin Ring Finger-1 Isoforms

Journal

GENESIS
Volume 47, Issue 8, Pages 524-534

Publisher

WILEY
DOI: 10.1002/dvg.20529

Keywords

Mahogunin ring finger-1; isoforms; spongiform neurodegeneration; pigmentation; craniofacial patterning; transgenesis

Funding

  1. NIA NIH HHS [R01 AG022058, R01 AG022058-05, R01 AG022058-04, R01 AG022058-01, R01 AG022058-02, R01 AG022058-03, R01AG022058] Funding Source: Medline

Ask authors/readers for more resources

Mahogunin Ring Finger-1 (Mgrn1) null mutant mice have a pleiotropic phenotype that includes the absence of yellow hair pigment, abnormal head shape, reduced viability, and adult-onset spongiform neurodegeneration. Mgm1 encodes a highly conserved E3 ubiquitin ligase with four different isoforms which are differentially expressed and predicted to localize to different subcellular compartments. To test whether loss of specific isoforms causes different aspects of the mutant phenotype, we generated transgenes for each isoform and bred them onto the null mutant background. Mice expressing only isoform I or III appeared completely normal. Isoform II rescued or partially rescued the mutant phenotypes, whereas isoform IV had little or no effect. Our data show that different Mgrn1 isoforms are not functionally equivalent in vivo and that the presence of only isoform I or III is sufficient for normal development, pigmentation, and neuronal integrity. genesis 47:524-534, 2009. (C) 2009 Wiley-Liss, Inc.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.0
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available