TGF-BETA-1 GENE-MUTATIONS IN INSULIN-DEPENDENT DIABETES-MELLITUS AND DIABETIC NEPHROPATHY

Citation
F. Pociot et al., TGF-BETA-1 GENE-MUTATIONS IN INSULIN-DEPENDENT DIABETES-MELLITUS AND DIABETIC NEPHROPATHY, Journal of the American Society of Nephrology, 9(12), 1998, pp. 2302-2307
Citations number
30
Categorie Soggetti
Urology & Nephrology
ISSN journal
10466673
Volume
9
Issue
12
Year of publication
1998
Pages
2302 - 2307
Database
ISI
SICI code
1046-6673(1998)9:12<2302:TGIIDA>2.0.ZU;2-Y
Abstract
PCR assays were established for easy and fast analysis of two transfor ming growth factor-beta 1 (TGF-beta 1) gene mutations, a C to T transi tion at position 76 in exon 5 resulting in a change from threonine to isoleucine in position 263 (Thr263Ile) of the propeptide and a deletio n of a C in the intron sequence eight bases prior to exon 5 (713-8delC ). These mutations were evaluated in insulin-dependent diabetes mellit us (IDDM) patients (n = 137) and control subjects (n = 105) and in IDD M patients with (n = 170) and without (n = 99) nephropathy. After eval uating intra- and interindividual variation in TGF-beta 1 expression l evels, the TGF-beta 1 mRNA level in phorbol 12-myristate-13-acetate-st imulated (1 ng/ml) lymphocytes from individuals with different TGF-bet a 1 genotypes was also studied. No association of the two TGF-beta 1 s equence variations with IDDM in general was found. However, a weak but significant association of the Thr263Ile mutation with diabetic nephr opathy was found (P = 0.03). No correlation between TGF-beta 1 transcr iption level and genotype of any of the two studied polymorphisms was found. However, significant interindividual differences in TGF-beta 1 mRNA levels were observed between the tested individuals (P < 0.0001) compatible with a genetic control mechanism of TGF-beta 1 synthesis at the mRNA level.