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
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.