NDLI: DAX1 mutations map to putative structural domains in a deduced three-dimensional model.

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DAX1 mutations map to putative structural domains in a deduced three-dimensional model.

Content Provider	World Health Organization (WHO)-Global Index Medicus
Author	Huang, B. L. Wagner, R. L. Nakamoto, J. Vilain, E. Anyane-Yeboa, K. Pagon, R. A. Rosenthal, I. M. Baxter, J. D. Klingensmith, G. J. McCabe, E. R. Zhang, Y. H. Burris, T. P. Chitayat, D. Pappas, J. G. Chudley, A. E. Genel, M. Burghes, A. H. Gertner, J. M. Levine, S. N. McCabe, L. New, M. I. Quigley, C. A. Fletterick, R. J. Guo, W.
Description	Country affiliation: United States Author Affiliation: Zhang YH ( Department of Pediatrics, UCLA School of Medicine, Los Angeles, CA, USA.)
Abstract	The DAX1 protein is an orphan nuclear hormone receptor based on sequence similarity in the putative ligand-binding domain (LBD). DAX1 mutations result in X-linked adrenal hypoplasia congenita (AHC). Our objective was to identify DAX1 mutations in a series of families, to determine the types of mutations resulting in AHC and to locate single-amino-acid changes in a DAX1 structural model. The 14 new mutations identified among our 17 families with AHC brought the total number of families with AHC to 48 and the number of reported mutations to 42; 1 family showed gonadal mosaicism. These mutations included 23 frameshift, 12 nonsense, and six missense mutations and one single-codon deletion. We mapped the seven single-amino-acid changes to a homology model constructed by use of the three-dimensional crystal structures of the thyroid-hormone receptor and retinoid X receptor alpha. All single-amino-acid changes mapped to the C-terminal half of the DAX1 protein, in the conserved hydrophobic core of the putative LBD, and none affected residues expected to interact directly with a ligand. We conclude that most genetic alterations in DAX1 are frameshift or nonsense mutations and speculate that the codon deletion and missense mutations give insight into the structure and function of DAX1.
ISSN	00029297
e-ISSN	15376605
Journal	The American Journal of Human Genetics
Issue Number	4
Volume Number	62
Language	English
Publisher	Cell Press (on behalf of American Society of Human Genetics)
Publisher Date	1998-04-01
Publisher Place	United States
Access Restriction	Open
Subject Keyword	Dna-binding Proteins Chemistry Genetics Mutation Receptors, Retinoic Acid Repressor Proteins Transcription Factors X Chromosome Adrenal Glands Abnormalities Amino Acid Sequence Dax-1 Orphan Nuclear Receptor Genetic Linkage Hypogonadism Molecular Sequence Data Sequence Analysis Structure-activity Relationship Research Support, Non-u.s. Gov't Research Support, U.s. Gov't, P.h.s. Discipline Human Genetics
Content Type	Text
Resource Type	Article
Subject	Genetics Genetics (clinical)

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