| Literature DB >> 11081182 |
O V Fofanova1, N Takamura, E Kinoshita, J S Parks, M R Brown, V A Peterkova, O V Evgrafov, N P Goncharov, A A Bulatov, I I Dedov, S Yamashita.
Abstract
Combined pituitary hormone deficiency (CPHD), including growth hormone (GH), prolactin (Prl) and thyroid-stimulating hormone (TSH) in children is now considered a heterogeneous syndrome. Recent findings on expression of mouse pituitary-specific homeodomain factors demonstrate dependence of adenopituitary ontogeny on interactive expression of these factors, suggesting their involvement in etiology of CPHD. Prophet of Pit-1 (Prop-1) gene, a novel pituitary-specific homeodomain factor, was analyzed in 14 Russian children with CPHD, in whom Pit-1 gene was intact. We found a mutational hot spot in three patients from two families in homeodomain part of the second exon of Prop-1 gene. The common 2-base pair deletion (GA296) in the homozygous state resulted in a Serine to Stop codon (S109X) substitution and generated a truncated Prop-1 protein. Parents were phenotypically normal and heterozygous for GA296 deletion, indicating an autosomal recessive inheritance. These results demonstrate a novel type of Prop-1 gene mutation as one of the causes of CPHD in Russian patients.Entities:
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Year: 1998 PMID: 11081182 DOI: 10.1023/a:1009918924945
Source DB: PubMed Journal: Pituitary ISSN: 1386-341X Impact factor: 4.107