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Abstract
The perinuclear theca (PT) is a unique cytoskeletal
structure that surrounds the nucleus of the sperm. The
posterior acrosome segment of the PT (postacrosomal PT) is
thought to play roles in shaping the nucleus during
differentiation of the spermatid and in activating the
oocyte during fertilization. We isolated a cDNA clone that
encoded a novel haploid germ cell-specific cysteine-rich
perinuclear theca protein, CYPT1. The transcripts were
expressed exclusively in testicular germ cells after
meiotic division. Sequence analysis revealed that CYPT1
comprised 168 amino acids and that the N-terminal was rich
in basic amino acids, including cysteine clusters.
Immunohistochemical and biochemical analyses localized
CYPT1 to the postacrosomal PT of elongated spermatids and
mature sperm. Cypt1 had three paralogs that were
expressed
in adult testis. A comparison of genomic structure
suggested that two of the three cypt1 paralogs were
generated by gene triplication on the X chromosome, while
one paralog was retrotransposed to an autosome.
Interestingly, the 5' flanking regions of these genes were
highly homologous with the promoter region of the
spermatid-specific gene Zfy-2. CYPT1 and the
proteins of
the paralogous genes constitute a novel, basic
cysteine-rich sperm protein family that contributes to the
function of the postacrosomal PT during nuclear shaping.
Key words:
Testis
Gametogenesis
Gene regulation
Sperm maturation
Spermatogenesis
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