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DAZ4  -  deleted in azoospermia 4

Homo sapiens

Synonyms: Deleted in azoospermia protein 4, pDP1680, pDP1681
 
 
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Disease relevance of DAZ4

  • DAZLA is a new member of the DAZ family of genes, which is associated with spermatogenesis and male sterility [1].
  • The evolution of the deleted in azoospermia (DAZ) gene family supports prevalent theories on the origin and development of sex chromosomes and sexual dimorphism [2].
  • The DAZ gene, a contributing factor in infertility, lies on the human Y chromosome's AZFc region, whose deletion is a common cause of spermatogenic failure [3].
 

High impact information on DAZ4

  • Genetic evidence has indicated that the DAZ family genes are critical for successful male germ cell development in diverse animals as well as humans [4].
  • A large AZFc deletion removes DAZ3/DAZ4 and nearby genes from men in Y haplogroup N [5].
  • Evolution of the DAZ gene family suggests that Y-linked DAZ plays little, or a limited, role in spermatogenesis but underlines a recent African origin for human populations [6].
  • It was found that human DAZ exons and introns are evolving at the same rate, implying neutral genetic drift and the absence of any functional selective pressures [6].
  • A new probe mapping on the deleted in azoospermia (DAZ) repetitive region of the Yq chromosome was designed for an early assessment of fetal DNA concentration in maternal serum [7].
 

Biological context of DAZ4

  • The deleted-in-azoospermia (DAZ) gene family constitutes the major candidate for the AZFc (azoospermia factor c) phenotype of male infertility, being deleted in about 10% of azoospermic and severely oligozoospermic subjects [8].
  • DAZ haplotypes were defined using single-nucleotide variant (SNV)/sequence tagged-site (STS) markers to distinguish between the four copies of the gene [3].
  • BACKGROUND: DAZ gene family is crucial for human spermatogenesis that requires the precise co-ordination of cell cycle events [9].
  • Quantitation of fetal DNA in maternal serum during the first trimester of pregnancy by the use of a DAZ repetitive probe [7].
  • The variation of 10 Y chromosome short tandem repeat (STRs) was used to determine the coalescence age of DAZ haplotypes in a comparable time frame similar to that of SNP haplogroups [3].
 

Anatomical context of DAZ4

  • The aim of the present study was to analyze the expression of the DAZ gene in seminiferous tubules of six men with spermatogenic disorders (hypospermatogenesis and spermatogenic arrest) [10].
  • In the patients with spermatogenic arrest at the spermatocyte stage, the DAZ gene transcripts were also found in primary spermatocytes [10].
  • The results of our study showed that DAZ gene activity seems to correspond to the proliferative activity of stem cells of germinal epithelium [10].
  • A protein in RAW 264.7 macrophages, which became phosphorylated in response to LPS (lipopolysaccharide), was identified as the RNA-binding protein called DAZAP1 [DAZ (deleted in azoospermia)-associated protein 1] [11].
 

Associations of DAZ4 with chemical compounds

  • Since SFV showed clearly the presence of DAZ2, it may be hypothesized that C5 lacks DAZ4 [12].
  • The mutation of Thr(269) and Thr(315) to aspartate or the phosphorylation of these residues caused DAZAP1 to dissociate from its binding partner DAZ [11].
 

Analytical, diagnostic and therapeutic context of DAZ4

  • Southern blot analysis showed that DAZLA is autosomal in all mammals tested and that DAZ has been recently translocated to the Y chromosome, sometime after the divergence of Old World and New World primates [1].
  • Real-time PCR with the use of DAZ multilocus probe can efficiently quantitate free fetal DNA in the maternal serum at the beginning of pregnancy [7].
  • The results based on the RT-PCR IS technique demonstrated that the DAZ product was present only in some seminiferous tubules and the fluorescence intensity was different within individual tubules [10].
  • With each hearing aid prescription, the ability of the hearing aid circuitry to reduce the effects of noise was evaluated by a sentence-in-noise test in three conditions: (1) adaptive directional microphone (DAZ), (2) multichannel noise reduction system (FNC), and (3) a combination of FNC and DAZ (FNC + DAZ) [13].

References

  1. Gene sequence, localization, and evolutionary conservation of DAZLA, a candidate male sterility gene. Seboun, E., Barbaux, S., Bourgeron, T., Nishi, S., Agulnik, A., Egashira, M., Nikkawa, N., Bishop, C., Fellous, M., McElreavey, K., Kasahara, M., Algonik, A. Genomics (1997) [Pubmed]
  2. Single-nucleotide variant in multiple copies of a deleted in azoospermia (DAZ) sequence - a human Y chromosome quantitative polymorphism. Szmulewicz, M.N., Ruiz, L.M., Reategui, E.P., Hussini, S., Herrera, R.J. Hum. Hered. (2002) [Pubmed]
  3. DAZ gene copies: evidence of Y chromosome evolution. Fernandes, A.T., Fernandes, S., Gonçalves, R., Sá, R., Costa, P., Rosa, A., Ferrás, C., Sousa, M., Brehm, A., Barros, A. Mol. Hum. Reprod. (2006) [Pubmed]
  4. Dazl can bind to dynein motor complex and may play a role in transport of specific mRNAs. Lee, K.H., Lee, S., Kim, B., Chang, S., Kim, S.W., Paick, J.S., Rhee, K. EMBO J. (2006) [Pubmed]
  5. A large AZFc deletion removes DAZ3/DAZ4 and nearby genes from men in Y haplogroup N. Fernandes, S., Paracchini, S., Meyer, L.H., Floridia, G., Tyler-Smith, C., Vogt, P.H. Am. J. Hum. Genet. (2004) [Pubmed]
  6. Evolution of the DAZ gene family suggests that Y-linked DAZ plays little, or a limited, role in spermatogenesis but underlines a recent African origin for human populations. Agulnik, A.I., Zharkikh, A., Boettger-Tong, H., Bourgeron, T., McElreavey, K., Bishop, C.E. Hum. Mol. Genet. (1998) [Pubmed]
  7. Quantitation of fetal DNA in maternal serum during the first trimester of pregnancy by the use of a DAZ repetitive probe. Stanghellini, I., Bertorelli, R., Capone, L., Mazza, V., Neri, C., Percesepe, A., Forabosco, A. Mol. Hum. Reprod. (2006) [Pubmed]
  8. A novel approach for the analysis of DAZ gene copy number in severely idiopathic infertile men. Ferlin, A., Moro, E., Rossi, A., Foresta, C. J. Endocrinol. Invest. (2002) [Pubmed]
  9. Association of spermatogenic failure with decreased CDC25A expression in infertile men. Cheng, Y.S., Kuo, P.L., Teng, Y.N., Kuo, T.Y., Chung, C.L., Lin, Y.H., Liao, R.W., Lin, J.S., Lin, Y.M. Hum. Reprod. (2006) [Pubmed]
  10. Localization of the DAZ gene expression in seminiferous tubules of patients with spermatogenic disorders. Szczerba, A., Jankowska, A., Andrusiewicz, M., Warchoł, J.B. Folia Histochem. Cytobiol. (2006) [Pubmed]
  11. Phosphorylation of the ARE-binding protein DAZAP1 by ERK2 induces its dissociation from DAZ. Morton, S., Yang, H.T., Moleleki, N., Campbell, D.G., Cohen, P., Rousseau, S. Biochem. J. (2006) [Pubmed]
  12. Quantitative evaluation of partial deletions of the DAZ gene cluster. D'Amico, G.L., Di Benedetto, D., Pezzino, F.M., Giuffrida, V., Libra, M., Fichera, M., Mauceri, G., Rappazzo, G., D'Agata, R., Vicari, E., Travali, S., Calogero, A.E. Int. J. Mol. Med. (2006) [Pubmed]
  13. Comparative performance of an adaptive directional microphone system and a multichannel noise reduction system. Yuen, K.C., Kam, A.C., Lau, P.S. Journal of the American Academy of Audiology. (2006) [Pubmed]
 
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