PGT-SR: A Comprehensive Overview and a Requiem for the Interchromosomal Effect

D. Griffin, C. Ogur
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Abstract

Preimplantation genetic testing for structural rearrangements (PGT-SR) was one of the first applications of PGT, with initial cases being worked up in the Delhanty lab. It is the least well-known of the various forms of PGT but nonetheless provides effective treatment for many carrier couples. Structural chromosomal rearrangements (SRs) lead to infertility, repeated implantation failure, pregnancy loss, and congenitally affected children, despite the balanced parent carrier having no obvious phenotype. A high risk of generating chromosomally unbalanced gametes and embryos is the rationale for PGT-SR, aiming to select for those that are chromosomally normal, or at least balanced like the carrier parent. PGT-SR largely uses the same technology as PGT-A, i.e., initially FISH, superseded by array CGH, SNP arrays, Karyomapping, and, most recently, next-generation sequencing (NGS). Trophectoderm biopsy is now the most widely used sampling approach of all PGT variants, though there are prospects for non-invasive methods. In PGT-SR, the most significant limiting factor is the availability of normal or balanced embryo(s) for transfer. Factors directly affecting this are rearrangement type, chromosomes involved, and sex of the carrier parent. De novo aneuploidy, especially for older mothers, is a common limiting factor. PGT-SR studies provide a wealth of information, much of which can be useful to genetic counselors and the patients they treat. It is applicable in the fundamental study of basic chromosomal biology, in particular the purported existence of an interchromosomal effect (ICE). An ICE means essentially that the existence of one chromosomal defect (e.g., brought about by malsegregation of translocation chromosomes) can perpetuate the existence of others (e.g., de novo aneuploidy). Recent large cohort studies of PGT-SR patients seem, however, to have laid this notion to rest, at least for human embryonic development. Unless new evidence comes to light, this comprehensive review should serve as a requiem.
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PGT-SR:染色体间效应的全面概述和安魂曲
植入前结构重排基因检测(PGT-SR)是PGT的首批应用之一,最初的病例在Delhanty实验室进行。它是各种形式的PGT中最不知名的,但仍然为许多携带者夫妇提供了有效的治疗。结构染色体重排(SRs)会导致不孕、重复植入失败、妊娠失败和先天性影响儿童,尽管平衡的父母携带者没有明显的表型。产生染色体不平衡配子和胚胎的高风险是PGT-SR的基本原理,旨在选择染色体正常的配子和胚胎,或者至少像载体亲本一样平衡的配子和胚。PGT-SR在很大程度上使用与PGT-A相同的技术,即最初的FISH,被阵列CGH、SNP阵列、Karyomapping以及最近的下一代测序(NGS)所取代。尽管有非侵入性方法的前景,但对流层活检现在是所有PGT变体中使用最广泛的采样方法。在PGT-SR中,最重要的限制因素是可用于移植的正常或平衡胚胎。直接影响这一点的因素是重排类型、所涉及的染色体和携带者父母的性别。新发的非整倍体,尤其是对于年龄较大的母亲来说,是一个常见的限制因素。PGT-SR研究提供了丰富的信息,其中大部分对遗传咨询师及其治疗的患者有用。它适用于基本染色体生物学的基础研究,特别是所谓的染色体间效应(ICE)的存在。ICE本质上意味着一种染色体缺陷的存在(例如,由易位染色体的不完全分离引起的)可以使其他染色体缺陷(例如,从头非整倍体)的存在永久化。然而,最近对PGT-SR患者的大型队列研究似乎已经打消了这一想法,至少对人类胚胎发育来说是这样。除非有新的证据曝光,否则这篇全面的综述应该是一首安魂曲。
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