Romano Maurizio, Bacalini Maria Giulia, Verschoor Ernst J, Crovella Sergio, Baralle Francisco E
International Centre for Genetic Engineering and Biotechnology, Padriciano 99, I-34012 Trieste, Italy.
FEBS Lett. 2008 Feb 6;582(3):423-6. doi: 10.1016/j.febslet.2007.12.038. Epub 2008 Jan 15.
The c.[833C; 844_845ins68] is a common haplotype of the human cystathionine beta-synthase gene among healthy individuals. This polymorphism (5-40% allelic frequency in different populations) consists of the c.844_845ins68 insertion that segregates in cis with the pathogenic c.833T>C substitution (p.I278T). Through genotyping of primates, we have found that gorillas, chimpanzees and bonobos are homozygous for the 68bp insertion, c.844_845ins68. In gorillas and bonobos, the c.844_845ins68 lesion segregates in cis with the wild-type c.833T variant, whilst chimpanzees present the human haplotype. These genetic evidences suggest that the origin of the 68bp insertion might be dated back to 6-8 million years ago, and that the c.833T>C substitution occurred within the allele carrying the insertion. The evolutionary conservation of this peculiar haplotype supports the hypothesis of its protective effects against cardiovascular diseases.
c.[833C; 844_845ins68]是健康个体中人类胱硫醚β-合酶基因的一种常见单倍型。这种多态性(在不同人群中等位基因频率为5 - 40%)由c.844_845ins68插入组成,该插入与致病性的c.833T>C替换(p.I278T)顺式分离。通过对灵长类动物进行基因分型,我们发现大猩猩、黑猩猩和倭黑猩猩对于68bp插入(c.844_845ins68)是纯合的。在大猩猩和倭黑猩猩中,c.844_845ins68损伤与野生型c.833T变体顺式分离,而黑猩猩呈现出人类单倍型。这些遗传学证据表明68bp插入的起源可能追溯到600 - 800万年前,并且c.833T>C替换发生在携带该插入的等位基因内。这种特殊单倍型的进化保守性支持了其对心血管疾病具有保护作用的假说。