Previous studies from this laboratory on hamster spermatozoa have demo
nstrated that rodent sperm DNA is packaged into the sperm nucleus in a
specific manner by nuclear structures. The entire genome is organized
into DNA loop domains attached at their bases to a sperm nuclear matr
ix, the skeletal structure of the nucleus. When nuclei are completely
decondensed, the nuclear matrix dissipates, and the entire genome rema
ins anchored to a single structure located at the base of the tail, te
rmed the nuclear annulus. Here, we have extended these studies to huma
n sperm nuclei, which were found to be similar to hamster. Human sperm
DNA was found to be organized into loop domains attached at their bas
es to a nuclear matrix. The average size of the human sperm halo of DN
A surrounding the extracted sperm nucleus (made up of DNA loop domains
) was about 50% smaller than those that have been reported for somatic
cells (this corresponds to an approximate loop domain size of 26.8 +/
- 2.1 kb). Human sperm DNA also remained anchored to the base of the t
ail when completely decondensed, indicating the existence of a nuclear
annulus-like structure in human spermatozoa; but, unlike the hamster
nuclear annulus, the human annulus could not be isolated because of it
s structural instability when separated from the tail. Using human cen
tromere repeats as a probe for in situ hybridization, we examined the
packaging of individual DNA sequences within the sperm nucleus. These
studies demonstrate that human sperm DNA is highly organized by nuclea
r structures.