Edward Heather L, Pisani Louis Almero Du, Rodriguez-Romero Walter E, Chaves-Villalobos Jorge, Garcia-Quesada Jonielle, Harris Neil S, Luo Hong-Yuan, Steinberg Martin H, Forget Bernard G, Chui David H K
Departments of Medicine, and Pathology and Laboratory Medicine, Division of Hematology/Oncology, Boston University School of Medicine , Boston, Massachusetts , USA .
Hemoglobin. 2014;38(6):381-4. doi: 10.3109/03630269.2014.971960. Epub 2014 Oct 27.
Hb Youngstown is a rare hemoglobin (Hb) variant caused by substitution of glutamic acid with alanine at amino acid residue 101 of the β-globin chain as a result of an A > C transversion on the β-globin gene nucleotide sequences [β101(G3)Glu → Ala; HBB: c.305A > C]. We now report three patients from two different families, one from South Africa and the other from Costa Rica, who are heterozygous for this Hb variant. All three carriers had marked hemolysis, consistent with Hb Youngstown being a highly unstable variant. The substitution of glutamic acid, a large and negatively charged amino acid, with alanine, a small and non polar amino acid, in the interface of the α1- and β2-globin subunits might interfere with the transition between the oxy- and deoxyHb, and lead to Hb instability and hemolytic anemia.
扬斯敦血红蛋白(Hb Youngstown)是一种罕见的血红蛋白(Hb)变体,它是由于β-珠蛋白基因核苷酸序列上发生A>C颠换,导致β-珠蛋白链第101位氨基酸残基处的谷氨酸被丙氨酸取代所致[β101(G3)Glu→Ala;HBB:c.305A>C]。我们现在报告来自两个不同家庭的三名患者,一名来自南非,另一名来自哥斯达黎加,他们都是这种Hb变体的杂合子。所有三名携带者都有明显的溶血现象,这与扬斯敦血红蛋白是一种高度不稳定的变体一致。在α1-和β2-珠蛋白亚基的界面处,大的带负电荷的氨基酸谷氨酸被小的非极性氨基酸丙氨酸取代,可能会干扰氧合血红蛋白和脱氧血红蛋白之间的转变,并导致血红蛋白不稳定和溶血性贫血。