Abstract
The prevalence of obesity and diabetes changes dramatically with lifestyle and unequal risk among individuals have made scientists interested to understand how the environment interferes with genetic factors to make it so-called genetic predisposition. This study aimed to explore wherethe most variable region is in leptin gene and analyse microsatellite repeats with direct sequencing in Iraqis and compare our alleles with other populations as a risk for obesity and T2D predisposition. DNA was extracted from blood of 60 type 2 diabetics and 70 non diabetics individuals, LEP 5‛UTR, exon 2 and 3 were screened in 45 individuals (24 type 2 diabetes patients and 21 non- diabetics), LEP TTTC repeats region were amplified in all 130 participants from which 22 control samples were purified and sequenced, superimposed sequences were analyzed manually. Sequencing results showed G>A polymorphism (rs2167270) in 5‛UTR region. No polymorphisms detected in LEP exons 2 and 3. LEP microsatellites alleles were classified depending on sizes into class1 < (220bp) and class2 (> 220bp). Analysis of 22 control samples sequences of microsatellite region resulted in 6 type1 allele (unique sequence) and 5 type 3 allele (13 different isoforms) depending on TTTC arrangement separated by Ts bases. We concluded that LEP variations were in non- coding regions and no significant difference was observed in allele frequency between both groups, but there was a huge diversity in microsatellite repeat number and context among individuals. This may affects gene function thus prepare a predisposition for obesity and type 2 diabetes.