Occurrence of Small, Round Vesicles in the Acrosome of Elongating Spermatids from a Mouse Mutant Line with Partial Deletion of the Y Chromosome

To elucidate abnormality of acrosome formation in germ cells of the B10.BR-Ydel (Ydel) mutant mouse, male mouse lines were produced by crossing the Ydel males with females from a transgenic mouse line, Acr-EGFP, carrying a transgene encoding a fusion protein of mouse pre-proacrosin and jellyfish enhanced green fluorescence protein (EGFP) under the control of the promoter of the mouse acrosin gene. Morphological analysis indicated that green fluorescence due to EGFP was non-uniformly localized in the acrosomal cap regions of cauda epididymal sperm in Ydel/Acr-EGFP mouse sperm. When spermatogenic cells at twelve stages of the seminiferous epithelial cycle were examined, no significant difference of the acrosome formation was observed between the wild-type and Ydel/Acr-EGFP mice, except that small, round vesicles without green fluorescence were frequently found in the acrosome of elongating spermatids at stage IX and later stages only in the mutant mouse. Some fluorescence-less vesicles were eliminated from the acrosome of elongating spermatids during late spermiogenesis. However, most of the fluorescence-less vesicles were retained in the acrosome. These results suggest that the occurrence of the small, round vesicles within the acrosome may correlate with the production of abnormal sperm with flat heads in the Ydel mutant mouse.

[1]  S. Conway,et al.  Y353/B: a candidate multiple-copy spermiogenesis gene on the mouse Y chromosome , 1994, Mammalian Genome.

[2]  M. Parvinen,et al.  Identification of living spermatogenic cells of the mouse by transillumination-phase contrast microscopic technique for ‘in situ’ analyses of DNA polymerase activities , 2004, Histochemistry.

[3]  M. Ikawa,et al.  Alkalinization of acrosome measured by GFP as a pH indicator and its relation to sperm capacitation. , 2001, Developmental biology.

[4]  A. Fukamizu,et al.  Identification of a novel isoform of poly(A) polymerase, TPAP, specifically present in the cytoplasm of spermatogenic cells. , 2000, Developmental biology.

[5]  S. Bhasin,et al.  The role of Y chromosome deletions in male infertility. , 2000, European journal of endocrinology.

[6]  M. Ikawa,et al.  Real‐time observation of acrosomal dispersal from mouse sperm using GFP as a marker protein , 1999, FEBS letters.

[7]  P. Reddi,et al.  Green fluorescent protein as a reporter for promoter analysis of testis-specific genes in transgenic mice. , 1999, Methods in enzymology.

[8]  H. Krzanowska,et al.  Sperm select penetration test reveals differences in sperm quality in strains with different Y chromosome genotype in mice. , 1995, Archives of andrology.

[9]  M. Sutcliffe,et al.  Fertility in mice requires X-Y pairing and a Y-chromosomal “Spermiogenesis” gene mapping to the long arm , 1992, Cell.

[10]  K. Naito,et al.  Effect of a partial deletion of Y chromosome on in vitro fertilizing ability of mouse spermatozoa. , 1992, Biology of reproduction.

[11]  J. Styrna,et al.  Influence of partial deletion of the Y chromosome on mouse sperm phenotype. , 1991, Journal of reproduction and fertility.

[12]  J. Styrna,et al.  An increased level of sperm abnormalities in mice with a partial deletion of the Y chromosome. , 1991, Genetical research.

[13]  H. Krzanowska The passage of abnormal spermatozoa through the uterotubal junction of the mouse. , 1974, Journal of reproduction and fertility.

[14]  Y. Toyoda Studies on fertilization of mouse eggs in vitro. I. In vitro fertilization of eggs by fresh epididymal sperm , 1971 .

[15]  E. Oakberg A description of spermiogenesis in the mouse and its use in analysis of the cycle of the seminiferous epithelium and germ cell renewal. , 1956, The American journal of anatomy.