首页> 外文期刊>Bone marrow transplantation >Comparison of short tandem repeat and variable number tandem repeat genetic markers for quantitative determination of allogeneic bone marrow transplant engraftment.
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Comparison of short tandem repeat and variable number tandem repeat genetic markers for quantitative determination of allogeneic bone marrow transplant engraftment.

机译:短串联重复序列和可变数目串联重复序列遗传标记的比较,用于定量测定同种异体骨髓移植的植入物。

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Variable number tandem repeats (VNTRs) were among the first genetic markers used to quantitate bone marrow transplant engraftment. The limitations of PCR-based VNTR markers in distinguishing some donor/recipient pairs has shown the need for additional genetic markers to analyze engraftment. Short tandem repeats (STRs) provide an excellent tool for this purpose because of their high degree of polymorphism and relatively short length. We compared STR analysis results with previous VNTR results for 16 post-transplantation samples from four allogeneic bone marrow transplant patients. Previously analyzed patient samples were chosen to cover the full range of engraftment. DNA samples from each patient were analyzed in a blinded fashion. Good quantitative correlation was found between STR and VNTR results in samples from all four patients. STR markers were informative in one patient for whom PCR-based VNTR markers were not available. Correlation of VNTR and STR methods helps to validate the use of STRs for the quantitative analysis of bone marrow transplant engraftment. This study demonstrates that STR-based human identity testing kits are well suited for engraftment analysis.
机译:可变数目的串联重复序列(VNTR)是用于定量骨髓移植植入的最早的遗传标记之一。基于PCR的VNTR标记在区分某些供体/受体对方面的局限性表明,需要更多的遗传标记来分析植入。短串联重复序列(STR)由于其高度的多态性和相对较短的长度而提供了出色的工具。我们将STR分析结果与先前的VNTR结果进行了比较,该结果来自4名同种异体骨髓移植患者的16个移植后样品。选择先前分析过的患者样本以覆盖整个植入范围。来自每个患者的DNA样品以盲法进行分析。在所有四名患者的样本中,STR和VNTR结果之间都存在良好的定量相关性。 STR标记物在没有基于PCR的VNTR标记物的一名患者中提供了很多信息。 VNTR和STR方法的相关性有助于验证将STR用于骨髓移植植入物定量分析的有效性。这项研究表明基于STR的人类身份测试套件非常适合植入分析。

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