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首页> 外文期刊>Animal Genetics >Chimaerism detection in bovine twins, triplets and quadruplets using sex chromosome-linked markers.
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Chimaerism detection in bovine twins, triplets and quadruplets using sex chromosome-linked markers.

机译:使用性染色体相关标记在双胞胎,三胞胎和四胞胎中进行嵌合体检测。

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摘要

The phenomenon of chimaerism occurs in the majority of cattle twin pregnancies. The objectives of this study were to develop a powerful diagnostic test for chimaerism in bovine male and female co-twins using X and Y chromosome-linked markers and to determine the extent of chimaerism in twins, triplets and quadruplets. We developed a multiplex PCR set of three polymorphic markers on chromosome X (DIK2865, DIK2283, AGLA257), where the presence of >1 and >2 alleles per marker is sufficient to prove chimaerism in males and females, respectively. In addition, a specific segment on chromosome Y (BOV97M) is included in the set to indicate chimaerism in females. Visualization of chimaeric alleles was best for DNA extracted from blood, fair for DNA from vaginal smears and failed for DNA extracted from hair. The power of chimaerism identification using this set of markers for DNA extracted from blood was calculated as 99% in males and virtually 100% in females. All females and males in heterosexual twins, triplets and quadruplets displayed evidence of a chimaeric allele in at least one and maximum of three of three X chromosome markers analysed. In addition, all females showed the presence of the BOV97M segment and were validated as chimaeric by the standard clinical diagnosis of impaired vaginal length. Quantitative PCR analysis of BOV97M copies in all twins vs. their sires showed a mean ratio of 45-68% in females and 39-49% in males, indicating a substantial symmetrical exchange of cells among all co-twins. The proposed analysis of X and Y chromosome-linked markers is advantageous to previous methods based on Y chromosome sequences only, because it detects chimaerism in both male and female co-twins.
机译:Chimaerism现象发生在大多数牛双胎妊娠中。这项研究的目的是使用X和Y染色体连锁的标记物对牛雄性和雌性双胞胎中的嵌合症进行强有力的诊断测试,并确定双胞胎,三胞胎和四胞胎中的嵌合症程度。我们在X染色体( DIK2865 , DIK2283 , AGLA257 )上建立了三个多态性标记的多重PCR组,其中存在> 1和>每个标记2个等位基因分别足以证明男性和女性的嵌合体。此外,Y染色体上的特定片段( BOV97M )也包含在该集合中,以指示女性的嵌合体。嵌合等位基因的可视化最适合于从血液中提取的DNA,对于阴道涂片中的DNA而言是公平的,而对于从头发中提取的DNA则失败。使用这组标记对从血液中提取的DNA进行化学手性鉴定的能力计算为,男性为99%,女性为100%。异性双胞胎,三胞胎和四胞胎中的所有雌性和雄性都显示出在至少三个分析的X染色体标记中至少有一个和最多三个中存在嵌合等位基因的证据。此外,所有女性均表现出 BOV97M 区段的存在,并通过标准的阴道长度受损临床诊断被确认为嵌合体。对所有双胞胎及其父亲的 BOV97M 拷贝进行的定量PCR分析表明,雌性的平均比率为45-68%,雄性的平均比率为39-49%,这表明所有共同双胞胎。建议的X和Y染色体连锁标记分析仅对以前基于Y染色体序列的方法有利,因为它可以检测男性和女性同卵双胞胎的嵌合现象。

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