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对无精子症男性进行基因谱分析,以确定病因并预测生殖潜能。

Genetic profiling of azoospermic men to identify the etiology and predict reproductive potential.

机构信息

The Ronald O. Perelman and Claudia Cohen Center for Reproductive Medicine, Weill Cornell Medicine, 1305 York Avenue, Y720, New York, NY, 10021, USA.

Department of Urology, James Buchanan Brady Foundation and Cornell Reproductive Medicine Institute, Weill Cornell Medicine, New York, NY, USA.

出版信息

J Assist Reprod Genet. 2024 Apr;41(4):1111-1124. doi: 10.1007/s10815-024-03045-5. Epub 2024 Feb 26.

Abstract

PURPOSE

To identify germline mutations related to azoospermia etiology and reproductive potential of surgically retrieved spermatozoa, and to investigate the feasibility of predicting seminiferous tubule function of nonobstructive azoospermic men by transcriptomic profiling of ejaculates.

MATERIALS AND METHODS

Sperm specimens were obtained from 30 men (38.4 ± 6 years) undergoing epididymal sperm aspiration for obstructive azoospermia (OA, n = 19) acquired by vasectomy, or testicular biopsy for nonobstructive azoospermia (NOA, n = 11). To evaluate for a correlation with azoospermia etiology, DNAseq was performed on surgically retrieved spermatozoa, and cell-free RNAseq on seminal fluid (n = 23) was performed to predict spermatogenesis in the seminiferous tubule.

RESULTS

Overall, surgically retrieved sperm aneuploidy rates were 1.7% and 1.8% among OA and NOA cohorts, respectively. OA men carried housekeeping-related gene mutations, while NOA men displayed mutations on genes involved in crucial spermiogenic functions (AP1S2, AP1G2, APOE). We categorized couples within each cohort according to ICSI clinical outcomes to investigate genetic causes that may affect reproductive potential. All OA-fertile men (n = 9) carried mutations in ZNF749 (sperm production), whereas OA-infertile men (n = 10) harbored mutations in PRB1, which is essential for DNA replication. NOA-fertile men (n = 8) carried mutations in MPIG6B (stem cell lineage differentiation), whereas NOA-infertile individuals (n = 3) harbored mutations in genes involved in spermato/spermio-genesis (ADAM29, SPATA31E1, MAK, POLG, IFT43, ATG9B) and early embryonic development (MBD5, CCAR1, PMEPA1, POLK, REC8, REPIN1, MAPRE3, ARL4C). Transcriptomic assessment of cell-free RNAs in seminal fluid from NOA men allowed the prediction of residual spermatogenic foci.

CONCLUSIONS

Sperm genome profiling provides invaluable information on azoospermia etiology and identifies gene-related mechanistic links to reproductive performance. Moreover, RNAseq assessment of seminal fluid from NOA men can help predict sperm retrieval during testicular biopsies.

摘要

目的

鉴定与无精子症病因和手术获取精子的生殖潜能相关的种系突变,并通过对精液进行转录组分析来研究预测非梗阻性无精子症男性的生精小管功能的可行性。

材料与方法

对 30 名因梗阻性无精子症(OA,n=19,因输精管结扎术获得)或非梗阻性无精子症(NOA,n=11,因睾丸活检获得)而接受附睾精子抽吸术的男性的精子标本进行研究。对手术获取的精子进行 DNAseq 检测,对精液进行游离 RNAseq 检测(n=23),以预测生精小管中的生精情况。

结果

总体而言,OA 和 NOA 队列中手术获取的精子非整倍体率分别为 1.7%和 1.8%。OA 男性携带管家基因相关突变,而 NOA 男性则携带与关键精子发生功能相关的基因突变(AP1S2、AP1G2、APOE)。我们根据 ICSI 临床结局将每个队列中的夫妇进行分类,以研究可能影响生殖潜能的遗传原因。所有 OA 生育男性(n=9)均携带 ZNF749 突变(精子生成),而 OA 不育男性(n=10)携带 PRB1 突变,后者对于 DNA 复制至关重要。NOA 生育男性(n=8)携带 MPIG6B 突变(干细胞谱系分化),而 NOA 不育男性(n=3)携带与精子发生相关的基因突变(ADAM29、SPATA31E1、MAK、POLG、IFT43、ATG9B)和早期胚胎发育(MBD5、CCAR1、PMEPA1、POLK、REC8、REPIN1、MAPRE3、ARL4C)。对 NOA 男性精液中的游离 RNA 进行转录组分析,可预测残留的生精灶。

结论

精子基因组分析提供了有关无精子症病因的宝贵信息,并确定了与生殖性能相关的基因机制联系。此外,对非梗阻性无精子症男性的精液进行 RNAseq 评估有助于预测睾丸活检时的精子获取。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57b5/11052749/2402dec82928/10815_2024_3045_Fig1_HTML.jpg

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