Shintani M, Minaguchi K, Isemura S, Saitoh E, Sanada K, Semba T
Department of Forensic Odontology, Tokyo Dental College, Chiba, Japan.
Hum Genet. 1994 Jul;94(1):45-9. doi: 10.1007/BF02272840.
A new genetic polymorphism of cystatin SA has been identified in human submandibular-sublingual saliva by means of basic gel electrophoresis and immunoblotting with anti-cystatin S. Two proteins, SA1 and SA2, are given by two alleles of CST2, viz., CST21 and CST2. Inheritance is controlled by two codominant alleles at an autosomal locus. This hypothesis is supported by studies of 16 families 32 children. Gene frequencies for CST21 and CST22 are 0.935 and 0.065, respectively (n = 341). Eighteen amino acids determined among 20 N-terminal residues of cystatin SA2 are identical with the sequence encoded by CST2. Three forms of cystatin S (mono-phosphorylated cystatin S, di-phosphorylated cystatin S, and non-phosphorylated cystatin S) are present in the 341 saliva samples tested.
通过碱性凝胶电泳和抗胱抑素S免疫印迹法,在人类颌下-舌下唾液中鉴定出一种新的胱抑素SA基因多态性。两种蛋白质SA1和SA2由CST2的两个等位基因即CST21和CST2产生。遗传由常染色体位点上的两个共显性等位基因控制。对16个家庭32名儿童的研究支持了这一假设。CST21和CST22的基因频率分别为0.935和0.065(n = 341)。在胱抑素SA2的20个N端残基中确定的18个氨基酸与CST2编码的序列相同。在测试的341份唾液样本中存在三种形式的胱抑素S(单磷酸化胱抑素S、双磷酸化胱抑素S和非磷酸化胱抑素S)。