MOLECULAR ANALYSIS OF GUANIDINOACETATE-N-METHYLTRANSFERASE (GAMT) AND CREATINE TRANSPORTER (SLC6A8) GENE BY USING DENATURING HIGH PRESSURE LIQUID CHROMATOGRAPHY (DHPLC) AS A POSSIBLE SOURCE OF HUMAN MALE INFERTILITY

被引:0
作者
Iqbal, Furhan [1 ,2 ]
Item, Chike Bellarmine [2 ]
Ratschmann, Rene [2 ]
Ali, Muhammad [3 ]
Plas, Eugen [4 ]
Bodamer, Olaf [2 ,5 ]
机构
[1] Bahauddin Zakariya Univ, Inst Pure & Appl Biol, Div Zool, Multan, Pakistan
[2] Med Univ Vienna, Lab Inherited Metab Disorders, Dept Pediat & Adolescent Med, Vienna, Austria
[3] Bahauddin Zakariya Univ, Inst Biotechnol, Multan, Pakistan
[4] KH Heitzing Neurol Zentrum, Dept Urol, A-1130 Vienna, Austria
[5] Paracelsus Med Sch Salzburg, Inst Inherited Metab Dis, Salzburg, Austria
关键词
Male infertility; creatine transporter; GAMT; DHPLC; INBORN ERROR; DEFICIENCY; IDENTIFICATION; METABOLISM; MUTATIONS;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The creatine/phosphocreatine system is essential for cellular phosphate coupled energy storage and production, particularly in tissues subject to high metabolic demands. Male factor infertility is a common condition with unknown etiology in most of the cases. Sperm abnormalities could possibly lead to infertility. As sperm motility depends on intact mitochondrial function and energy levels. Thus reduced intracellular creatine stores may contribute to decreased sperm motility leading to male infertility as creatine /phosphocreatine system plays major role in making and breaking of ATP, thus in energy kinetics. We developed and validated a denaturing high performance liquid chromatograph (DHPLC) method for the molecular analysis of SLC6A8 and GAMT genes involve in creatine biosynthesis and transport as a possible source of human male infertility by analyzing DNA from 64, clinically confirmed, infertile men. No mutation/polymorphism was detected in the exonic regions of both genes in all the patients and in fertile healthy controls indicating that SLC6A8 and GAMT genes may not be directly involved in human male infertility.
引用
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页码:75 / 79
页数:5
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