Romo-Martínez Enrique Jhonatan, Martínez-Cortés Gabriela, Barajas-Torres Reyna Lucía, Rubi-Castellanos Rodrigo, Magaña-Torres María Teresa, Rangel-Villalobos Héctor, González-García Juan Ramón
Departamento de Ingeniería en Biotecnología, Universidad Politécnica de Sinaloa, CP: 82199, Mazatlán, Sinaloa, México.
J Genet. 2012;91(3):297-302. doi: 10.1007/s12041-012-0187-x.
Morphological variation of the Y chromosome has been observed in different populations. This variation is mostly related to the heteromorphic Yq12 band, which is composed of a variable block of constitutive heterochromatin. The Yqh+ heteromorphism has a worldwide frequency of 2.85% and is considered clinically innocuous. The aim of this study was to identify the ancestry of the Yqh+ heteromorphism present in individuals from western Mexico. For this purpose, 17 Y-chromosome single nucleotide polymorphisms were analysed by multiplex polymerase chain reaction and SNaPshot assays. In 28 Yqh+ males, only five haplogroups were observed; with a haplogroup diversity of 0.4841 ± 0.1094, which was less than that observed in a study of unselected Mexican mestizo population. Differences were specifically conferred by the high frequencies of haplogroups R1b1 and P*(xQ,R), and by the absence of the Amerindian haplogroup Q (Q*(xQ1a3a) plus Q1a3a) from the Yqh+ group. This study suggests a post-1492 incorporation for Yqh+ chromosomes into the Mexican northwestern population.
在不同人群中已观察到Y染色体的形态变异。这种变异大多与异态的Yq12带有关,该带由组成型异染色质的可变区域构成。Yqh +异态在全球的出现频率为2.85%,被认为在临床上无害。本研究的目的是确定墨西哥西部个体中存在的Yqh +异态的祖先来源。为此,通过多重聚合酶链反应和SNaPshot分析检测了17个Y染色体单核苷酸多态性。在28名Yqh +男性中,仅观察到五个单倍群;单倍群多样性为0.4841±0.1094,低于对未选择的墨西哥混血人群的研究中观察到的多样性。差异具体表现为单倍群R1b1和P*(xQ,R)的高频率,以及Yqh +组中不存在美洲印第安单倍群Q(Q*(xQ1a3a)加Q1a3a)。本研究表明,Yqh +染色体在1492年后融入了墨西哥西北部人群。