Kw. Wolf et Bm. Turner, THE PATTERN OF HISTONE H4 ACETYLATION ON THE X-CHROMOSOME DURING SPERMATOGENESIS OF THE DESERT LOCUST SCHISTOCERCA-GREGARIA, Genome, 39(5), 1996, pp. 854-865
We have used antibodies directed against histone H4 acetylated at lysi
ne residue 5, 8, 12, or 16 and indirect immunofluorescence microscopy
to probe chromosomes from spermatogonia and spermatocytes of the deser
t locust, Schistocerca gregaria. The autosomes showed bright overall f
luorescence, indicative of high levels of H4 acetylation. In contrast,
the X chromosome, which is facultatively heterochromatic during sperm
atogenesis of the locust, remained completely unstained in spermatogon
ia and secondary spermatocytes and showed only a small terminal fluore
scent band in primary spermatocytes. This band probably corresponds to
centromere- associated constitutive heterochromatin. Thus, underacety
lation is a cytogenetic marker for facultative heterochromatin, but no
t necessarily constitutive heterochromatin, during spermatogenesis of
the locust. Scanning electron microscopy of chromosomes from prophase
spermatogonia and prophase I spermatocytes revealed that underacetylat
ion of histone H4 in the X chromosome was not accompanied by a chromat
in organization visibly different from that of the autosomes. Transmis
sion electron microscopy of mitotic spermatogonia showed that the X ch
romosome is separated from the autosomes in a small nuclear compartmen
t of its own in prophase and telophase and associated with membranes i
n metaphase. In prophase I spermatocytes, autosomes and the sex unival
ent were in the same compartment. This compartmentalization may be res
ponsible for the underacetylation and (or) transcriptional silencing o
f the X chromosome in spermatogonial mitosis.