Table of Contents  
LETTER TO THE EDITOR
Year : 2014  |  Volume : 16  |  Issue : 6  |  Page : 931-933

Association of PIWIL4 genetic variants with germ cell maturation arrest in infertile Spanish men


1 Human Molecular Genetics Group, Bellvitge Biomedical Research Institute, IDIBELL, L'Hospitalet de Llobregat, Barcelona, Spain
2 Laboratory of Seminology and Embryology, Andrology Service-Fundació Puigvert, Barcelona, Spain

Date of Submission25-Jan-2014
Date of Decision26-Feb-2014
Date of Acceptance15-Mar-2014
Date of Web Publication10-Jun-2014

Correspondence Address:
Sara Larriba
Human Molecular Genetics Group, Bellvitge Biomedical Research Institute, IDIBELL, L'Hospitalet de Llobregat, Barcelona
Spain
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/1008-682X.131069

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How to cite this article:
Munoz X, Navarro M, Mata A, Bassas L, Larriba S. Association of PIWIL4 genetic variants with germ cell maturation arrest in infertile Spanish men. Asian J Androl 2014;16:931-3

How to cite this URL:
Munoz X, Navarro M, Mata A, Bassas L, Larriba S. Association of PIWIL4 genetic variants with germ cell maturation arrest in infertile Spanish men. Asian J Androl [serial online] 2014 [cited 2019 Oct 24];16:931-3. Available from: http://www.ajandrology.com/text.asp?2014/16/6/931/131069 - DOI: 10.4103/1008-682X.131069

Dear Editor,

The PIWI proteins (originally P-element-induced wimpy testis in Drosophila) are predominantly present in the germ-line in diverse organisms and are involved in the processing of a class of small RNAs known as piRNAs (see Refs. [1]],[[2] for review). The human PIWI protein family consists of four members: PIWIL1-4. Of these, PIWIL4 is known to have essential roles in the first phases of spermatogenesis: its expression is restricted to gonocytes and it is required for transposon silencing. [3] The lack of this gene in mice causes meiotic arrest in spermatogenesis. [4] The goal of our study was to evaluate the frequency of several PIWIL4 genetic variants in our population to better define the relationship between PIWIL4 single nucleotide polymorphisms (SNPs) and both defective spermatogenesis and specific spermatogenic disorders.

We have genotyped four PIWIL4 SNPs (rs7110167 C/T, exon 7-synonimous; rs57607909 G/C, exon 9-missense; rs593690 T/C, exon 13-synonimous, and rs508485 C/T, 3'UTR) [Table 1], with a reported minor allele frequency (MAF) of >0.05 in the general Caucasian population (HapMap CEU), in genomic DNA from 79 nonobstructive infertile men (patients) with azoospermia (n = 61) or severe oligozoospermia (sperm counts <5 × 10 6 ml−1 ; n = 18), and 56 men diagnosed with obstructive azoospermia (as a consequence of congenital absence of the vas deferens or a previous vasectomy), who showed conserved spermatogenesis (controls). Patients underwent testicular biopsy, which showed a histological pattern with a total absence of germ cells (Sertoli cell-only syndrome, SCO; n = 40), >90% of maturation arrest, either in spermatogonia or in primary spermatocytes (MA; n = 22) and hypospermatogenesis (HS; n = 17). Men with a chromosomal aberration or with a Y-chromosome microdeletion had been previously excluded from the study. All the men included in this study were recruited from the Andrology Service of Fundaciσ Puigvert and gave their informed consent for the study, which was approved by the Institutional Ethical Committee. All of them were Caucasians of Spanish origin.
Table 1: Genetic description of PIWIL4 variants evaluated in our study

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The current method for SNP determination was allelic discrimination using a Real Time PCR System and SNP Genotyping Assays (Applied Biosystems, Foster City, CA, USA). The χ2 test using Fisher exact test to the 5% limit was employed to compare carrier and allele frequencies in the patients and controls. Hardy-Weinberg equilibrium was tested by the χ2 test. The significance level was established at P < 0.05. These statistical analyses were performed using the SPSS software version 12 (Lead Technologies, Chicago, USA). Pairwise linkage disequilibrium (LD) between SNPs, haplotype frequencies, and association analyses were performed with SNPassoc, genetics and haplo.stats in R package ( http://www.creal.cat/jrgonzalez/software.htm ).

Our results show that the SNPs rs7110167, rs57607909, and rs593690 were in LD [Figure 1] in our cohort of individuals (D' score >0.85), whereas rs508485 is independent of the other three (D' <0.12). No significant differences in frequencies of allele, allele carrier, and genotypes were observed between patients and controls at the rs7110167, rs57607909, and rs593690 loci. Interestingly, we found that the frequencies of allele T (61.4% vs. 40.2%; P = 0.021) and allele T carrier (CT + TT) (86.4% vs. 60.7%; P = 0.033) in MA patients were higher than they were in the controls at the rs508485 locus. When the genotype frequencies were compared between the groups, a difference in genotype distribution was found in MA versus controls, although it was not statistically significant (P = 0.06) [Table 2]. This SNP could have potential consequences for mRNA stability by altering the PIWIL4 3'UTR binding to miRNAs.
Figure 1: Linkage disequilibrium (LD) map of the PIWIL4 analyzed single nucleotide polymorphisms (SNPs), according to Haploview analysis (http://www.broadinstitute.org/scientific-community/software) of our population genotype data. Red boxes indicate strong evidence of LD according to D' (% values are indicated) while white ones indicate strong evidence of recombination.

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Table 2: Allele and genotype distributions of the four SNPs of PIWIL4 in infertile patients and controls

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To further investigate the relationship of the four SNP in PIWIL4 and defects in sperm production, we performed a haplotype analysis of these variants in patient and control groups. A total of six haplogroups were found in a frequency > 0.05 [Table 3]. The frequency of haplotype TGCT was higher in patients (29.4% vs. 18.9%; P = 0.036) and in SCO compared with controls (32.5% vs. 18.9%; P = 0.005), whereas a similar frequency of the haplotype TGCT was observed in HS and controls (17.6% vs. 18.9%). MA patients also presented a higher frequency of haplotype TGCT (33.4% vs. 18.9%; P = 0.24) and CGTT (14.3% vs. 7.6%; P = 0.24) than controls although the difference was not statistically significant, which is probably attributable to the low number of MA samples for the haplotype frequency estimation. Haplotypes CCTC (15.3% vs. 9.4%; P = 0.018) and CGTC (15.3% vs. 10.3%; P = 0.027) may also be risk factors for SCO infertility. A higher frequency of haplotype TGCT was also found in patients classified as azoospermic (29.3% vs. 18.9%; P = 0.036) and severely oligozoospermic (33.2% vs. 18.9%; P = 0.14), although the difference was not statistically significant for the oligozoospermic group; probably due to the lower number of samples.
Table 3: Haplotype frequencies of four SNPs of PIWIL4 and association with infertile phenotypes

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Our results bring additional information from different populations about the involvement of PIWIL4 genetic polymorphisms in spermatogenic failure. An association was previously observed in an infertile Chinese population: patients with at least one rs508485 variant allele had a statistically significant risk of oligozoospermia (sperm counts <20 × 10 6 ml−1 ), but not of azoospermia. [5] Our results contradict this as we have found this SNP to be associated with severe MA, a specific spermatogenic disorder leading to azoospermia. The cause of this discrepancy may be related to the influence of unknown ethnicity differences, but it could also be due to the absence of histological characterization of the infertile Chinese men. In fact, most of the testicular histological patterns in azoospermia correspond to SCO, which was not found to be associated with rs508485 SNP in the Spanish population. Under the assumption that genetic predisposition for spermatogenic impairment is most likely to be polygenic in nature, we conclude that genetic variants in PIWIL4 may contribute to the risk of spermatogenic deficiency in the Spanish population. We suggest that SNP rs508485, in the PIWIL4 gene is very likely to be relevant in genetic susceptibility to male infertility and specifically to premeiotic and meiotic maturation arrest, supporting the role of PIWI proteins in spermatogenesis and self-renewal of germ stem cells. [2] Our findings may help to increase the understanding of the PIWIL4 genetic contribution to male infertility by defining the testicular histological phenotype associated with the presence of specific SNPs in PIWIL4. Previous data have provided evidence that other members of the PIWI pathway are affected by epigenetic mechanisms in human spermatogenic failure. [6] Furthermore, the expression profile of transposon silencing genes (i.e. PIWIL2 and PIWIL4) was altered in azoospermia in cryptorchid boys. [7] These, together with our results suggest that genetic and epigenetic alterations that affect the PIWI pathway contribute to unsuccessful sperm production, which might explain a subset of male infertility disorders.


  Author Contributions Top


This study was conceived and designed by SL. Samples and clinical data were selected by AM and LB. Experiments were performed by MN and XM. Data were analyzed by XM, MN, LB, and SL. The manuscript was written by SL, and was critically revised by XM and LB. All authors read and approved the final manuscript.


  Competing Interests Top


The authors declare no competing interests.


  Acknowledgments Top


The authors are indebted to the patients that participated in this study. We thank Harvey Evans for the revision of the English text. This work was supported by grants from the Fondo de Investigaciones Sanitarias/Fondo Europeo de Desarrollo Regional (FIS/FEDER) (Nos. PI09/1727, PI12/00361) and the Generalitat de Catalunya (No. 2009SGR01490). SL is sponsored by the Researchers Stabilization Program from the Spanish National Health System (No. CES09/020).

 
  References Top

1.
Juliano C, Wang J, Lin H. Uniting germline and stem cells: the function of Piwi proteins and the piRNA pathway in diverse organisms. Annu Rev Genet 2011; 45: 447-69.  Back to cited text no. 1
    
2.
Bamezai S, Rawat VP, Buske C. Concise review: the Piwi-piRNA axis: pivotal beyond transposon silencing. Stem Cells 2012; 30: 2603-11.  Back to cited text no. 2
    
3.
Aravin AA, Sachidanandam R, Bourc'his D, Schaefer C, Pezic D, et al. A piRNA pathway primed by individual transposons is linked to de novo DNA methylation in mice. Mol Cell 2008; 31: 785-99.  Back to cited text no. 3
    
4.
Carmell MA, Girard A, van de Kant HJ, Bourc'his D, Bestor TH, et al. MIWI2 is essential for spermatogenesis and repression of transposons in the mouse male germline. Dev Cell 2007; 12: 503-14.  Back to cited text no. 4
    
5.
Gu A, Ji G, Shi X, Long Y, Xia Y, et al. Genetic variants in Piwi-interacting RNA pathway genes confer susceptibility to spermatogenic failure in a Chinese population. Hum Reprod 2010; 25: 2955-61.  Back to cited text no. 5
    
6.
Heyn H, Ferreira HJ, Bassas L, Bonache S, Sayols S, et al. Epigenetic disruption of the PIWI pathway in human spermatogenic disorders. PLoS One 2012; 7: e47892.  Back to cited text no. 6
    
7.
Hadziselimovic F, Hadziselimovic NO, Demougin P, Krey G, Oakeley EJ. Deficient expression of genes involved in the endogenous defense system against transposons in cryptorchid boys with impaired mini-puberty. Sex Dev 2011; 5: 287-93.  Back to cited text no. 7
    


    Figures

  [Figure 1]
 
 
    Tables

  [Table 1], [Table 2], [Table 3]


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