Table of Contents  
LETTER TO THE EDITOR
Year : 2015  |  Volume : 17  |  Issue : 5  |  Page : 857-858

An insertion mutation in the androgen receptor gene in a patient with azoospermia


1 Department of Surgery, Zhejiang Provincial Top Key Discipline in Surgery, Wenzhou Key Laboratory of Surgery, The First Affiliated Hospital, Wenzhou Medical University, Wenzhou 325000, China
2 Department of Urology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325000, China

Date of Submission21-Oct-2014
Date of Decision09-Dec-2014
Date of Acceptance30-Dec-2014
Date of Web Publication06-Feb-2015

Correspondence Address:
Zhi-Gang Wu
Department of Urology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325000
China
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/1008-682X.148724

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How to cite this article:
Chen YH, Xu HY, Wang ZY, Zhu ZH, Li CD, Wu ZG, Chen BC. An insertion mutation in the androgen receptor gene in a patient with azoospermia. Asian J Androl 2015;17:857-8

How to cite this URL:
Chen YH, Xu HY, Wang ZY, Zhu ZH, Li CD, Wu ZG, Chen BC. An insertion mutation in the androgen receptor gene in a patient with azoospermia. Asian J Androl [serial online] 2015 [cited 2019 Sep 19];17:857-8. Available from: http://www.ajandrology.com/text.asp?2015/17/5/857/148724 - DOI: 10.4103/1008-682X.148724

Dear Editor,

We present here a case of an infertile man with azoospermia, from whom an insertion mutation (g. 1283_1284insAGTTTGCTG) near the beginning of the CAG repeat in the exon 1 of androgen receptor (AR) gene is demonstrated.

The human AR is a ligand-activated transcription factor. Encoded by a single-copy gene located on Xq11-12, it is composed of 8 exons. [1] There are four domains in the protein structure, including the N-terminal transactivation domain (TAD) encoded by exon 1, DNA-binding domain encoded by exons 2 and 3, hinge region encoded by part of exon 4, and C-terminal ligand-binding domain encoded by exons 4-8. [2] The TAD consists of two polymorphic sites, characterized by different numbers of CAG and GGN repeats in exon 1, resulting in variable lengths of polyglutamine and polyglycine stretches. [3] Mutations in the AR gene may result in the androgen insensitivity syndrome (AIS) with various phenotypes in XY individuals. Males with Complete AIS (CAIS) show the female phenotype with female external genitalia. In partial AIS, the patients have genital ambiguity while males with mild AIS (MAIS) are phenotypically normal with or without normal spermatogenesis. [4]

More than 1000 mutations in the AR gene have been reported, most of which pertains to substitutions leading to transformations of proteins. Variations of insertions or duplications are rare, and the overwhelming majority of them are in regard to CAIS.

A 25-year-old infertile man presented to our department with a history of hypoplasia of testis. The scrotum was small and testes were palpable but decreased in size, with a one-sided testicular volume of 4 ml measured by an orchidometer. Routine examination of semen was conducted with the consequence indicating the volume and pH of semen was normal (2.2 ml and 7.2 ml, respectively), however, the total amount and concentration of spermatozoa were down to zero. In addition, no sperm could be detected even after centrifugation. Scrotum biopsy failed by the rejection of patient ([Table 1]). Hormonal evaluation revealed that total testosterone (T), free T and estradiol were in the physiological range (16.62 nmol l−1 , 43.06 pg l−1 and 111.0 pmol l−1 , respectively), whereas luteinizing hormone (LH, 17.00 IU l−1 ) and follicle stimulating hormone (FSH, 49.70 IU l−1 ) were in high levels ([Table 1]).
Table 1: Hormonal features and examination of semen in the patient


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Eight AR exons were sequenced from the patient, and molecular genetic testing of the AR gene revealed a mutation in exon 1, which resulted in a glutamine to leucine substitution at codon 58, caused by a CAG to CTG transversion. Besides, a more remarkable variation (g. 1283_1284insAGTTTGCTG) was found between codon 56 and codon 57, which meant three proteins (serine-leucine-leucine) were added in [Figure 1]a. The point mutation was at the beginning of CAG repeat, and the insertion was close to it in the meanwhile. To predict how the mutation affected protein function and stability, SOPMA (http:@www.ibcp.fr/predict.html) prediction tool was performed. The results, to be specific, the ratio of four main spatial structures in normal and variant sequences were as follows: alpha helix 27.56%-25.10%, extended strand 9.06%-8.37%, beta-turn 1.57%-3.19%, and random coil 61.81%-63.35% ([Figure 1]b).
Figure 1: Results of sequencing and structure prediction. (a) ">0" and ">1" stand for sequences from the normal and the patient, respectively. Alignments of them revealed the insertion of three proteins including serine-leucine-leucine at codon 57 in yellow block, along with the point mutation at codon 58 in green block. (b) The ratio of four main spatial structures in normal and variant sequences was described with various colors: blue, red, green, and purple line represents alpha helix, extended strand, beta-turn, and random coil, respectively.

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The number of CAG and GGC triplets was determined during analysis of exon 1. The triplet number (21 CAG and 17 GGC) was within the normal range (10-35 and 4-24, respectively), [3] therefore, the possibility that the length of the CAG repeat contributed to infertility in this patient could be excluded, especially Kennedy's disease in which the number of CAG repeats exceeds 40. [5]

Routine examination of semen delivered signs that spermatogenesis may be impaired with no sperm being detected, which could be considered as azoospermia. It was reported that an elevated level of serum FSH, together with either normal or low serum T levels, was associated with primary testicular failure. In contrast, elevated serum LH levels with normal or elevated T levels indicated androgen resistance at the hypothalamic-pituitary level. [6] In this case, the elevation of LH was the consequence of an impaired negative feedback control of T on LH secretion due to insensibility of the AR. Then the deficiency of spermatozoa in patient might be responsible for the inverse feedback toward FSH. Consistent with the previous study, the T was within the normal level.

Exon 1, as the longest coding region of the AR gene, plays a significant role in regulating AR activity and encodes roughly 58% of the protein. [7] According to the AR gene mutations database (http://www.androgendb.mcgill.ca, last updated 2013), approximately 20.7% of entire mutations have been reported in exon 1, among which only 9.6% (mainly point mutations) result in the MAIS phenotype. Of the total, just 24 insertion mutations (about 2.2%) are covered, the majority of which occur in CAIS patients. Our finding differed from them with the insertion of nine nucleotides, which avoided causing a frame shift and stopping in advance. It meant the length and structure of proteins did not change violently, without contributing to CAIS. But obviously, it varied a lot from alterations caused merely by point mutations.

The p.Gln58Leu substitution presented in this study has been previously reported. [8] In accordance with the study, an extra leucine is located immediately upstream of the polyglutamine tract and is likely to slightly change the conformation of this domain, thereby perhaps altering interaction with other co-activators and/or repressors. Furthermore, together with notable changes that three proteins, Ser-Leu-Leu, inserted near the point mutation, the final result was that a chain of proteins involving five ones altered around the beginning of polyglutamine tract, from "LQ" to "SLLLL" ([Figure 1]a). With the help of SOPMA, we identified that the specific gravity of the alpha helix and extended strand reduced while beta turn and random coil structure increased. It demonstrated the variation induced a moderate change of the predicted protein structure in the TAD of the AR, where was known to interact with co-factors. [9],[10]

To testify the prevalence of insertion mutations associated with MAIS and damaged spermatogenesis, we analyzed relevant studies in exon 1 by AR database. Ferlin et al. [4] covered infertility in a subject with a mutation at codon 57 of the AR gene, with one leucine duplicated, the position of which was definitely identical to our finding. Our present case showed two more amino acids (serine and leucine) compared to them. Moreover, as the polyglutamine tract coded by the CAG repeat is involved in regulating the AR transactivation function, it is crucial to spermatogenesis. [8] Therefore, we believed that the protein function may be affected, for the variation was located near the beginning of polyglutamine, where was conserved region for the correct folding of AR protein and resemble outcomes could be referred.

However, for our expose of variation includes a substitution and an insertion, further studies are needed to elucidate the detailed roles of these mutations in male infertility separately.

In summary, an insertion mutation together with a known point variation was described in the TAD of AR gene. They could be responsible for the impaired spermatogenesis, and this research would enrich the AR database and extend the current understanding of AR pathology.


  Author Contributions Top


YHC carried out the genetic studies, conducted the analysis of mutations and drafted the manuscript. HYX and CDL participated in the acquisition, analysis, and interpretation of data. ZYW and ZHZ took part in data acquisition and sequence alignment. ZGW and BCC conceived the study and assisted to modify the manuscript. All authors read and approved the final manuscript.


  Competing Interests Top


The authors declared no competing interests.


  Acknowledgments Top


This study was supported by grants from Undergraduate Innovation Project of Wenzhou Medical University (wyx 201401007), and Undergraduate Scientific and Technological Innovation Project for Talent Program from Zhejiang Province.

 
  References Top

1.
Brown CJ, Goss SJ, Lubahn DB, Joseph DR, Wilson EM, et al. Androgen receptor locus on the human X chromosome: regional localization to Xq11-12 and description of a DNA polymorphism. Am J Hum Genet 1989; 44: 264-9.  Back to cited text no. 1
    
2.
Gottlieb B, Beitel LK, Wu JH, Trifiro M. The androgen receptor gene mutations database (ARDB): 2004 update. Hum Mutat 2004; 23: 527-33.  Back to cited text no. 2
    
3.
Ferlin A, Bartoloni L, Rizzo G, Roverato A, Garolla A, et al. Androgen receptor gene CAG and GGC repeat lengths in idiopathic male infertility. Mol Hum Reprod 2004; 10: 417-21.  Back to cited text no. 3
    
4.
Ferlin A, Vinanzi C, Garolla A, Selice R, Zuccarello D, et al. Male infertility and androgen receptor gene mutations: clinical features and identification of seven novel mutations. Clin Endocrinol (Oxf) 2006; 65: 606-10.  Back to cited text no. 4
    
5.
Goglia U, Vinanzi C, Zuccarello D, Malpassi D, Ameri P, et al. Identification of a novel mutation in exon 1 of androgen receptor gene in an azoospermic patient with mild androgen insensitivity syndrome: case report and literature review. Fertil Steril 2011; 96: 1165-9.  Back to cited text no. 5
    
6.
Gottlieb B, Lombroso R, Beitel LK, Trifiro MA. Molecular pathology of the androgen receptor in male (in) fertility. Reprod Biomed Online 2005; 10: 42-8.  Back to cited text no. 6
    
7.
Philibert P, Audran F, Pienkowski C, Morange I, Kohler B, et al. Complete androgen insensitivity syndrome is frequently due to premature stop codons in exon 1 of the androgen receptor gene: an international collaborative report of 13 new mutations. Fertil Steril 2010; 94: 472-6.  Back to cited text no. 7
    
8.
Lund A, Juvonen V, Lähdetie J, Aittomäki K, Tapanainen JS, et al. A novel sequence variation in the transactivation regulating domain of the androgen receptor in two infertile Finnish men. Fertil Steril 2003; 79 Suppl 3: 1647-8.  Back to cited text no. 8
    
9.
Hsiao PW, Lin DL, Nakao R, Chang C. The linkage of Kennedy's neuron disease to ARA24, the first identified androgen receptor polyglutamine region-associated coactivator. J Biol Chem 1999; 274: 20229-34.  Back to cited text no. 9
    
10.
Yu X, Li P, Roeder RG, Wang Z. Inhibition of androgen receptor-mediated transcription by amino-terminal enhancer of split. Mol Cell Biol 2001; 21: 4614-25.  Back to cited text no. 10
    


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