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Vol. 9, Issue 4, 733-747, April 1998
Department of Embryology, Carnegie Institution, Baltimore, Maryland
21210
We have examined the behavior of demembranated sperm heads when
injected into the germinal vesicle (GV) of amphibian oocytes. Xenopus sperm heads injected into Xenopus
GVs swelled immediately and within hours began to stain with an
antibody against RNA polymerase II (Pol II). Over time each sperm head
became a loose mass of chromosome-like threads, which by 24-48 h
resolved into individually recognizable lampbrush chromosomes (LBCs).
Although LBCs derived from sperm are unreplicated single chromatids,
their morphology and immunofluorescent staining properties were
strikingly similar to those of the endogenous lampbrush bivalents. They
displayed typical transcriptionally active loops extending from an axis of condensed chromomeres, as well as locus-specific "landmarks." Experiments with [3H]GTP and actinomycin D demonstrated
that transcription was not necessary for the initial swelling of the
sperm heads and acquisition of Pol II but was required for maintenance
of the lampbrush loops. Splicing was not required at any stage during
formation of sperm LBCs. When Xenopus sperm heads were
injected into GVs of the newt Notophthalmus, the
resulting sperm LBCs displayed very long loops with pronounced Pol II
axes, like those of the endogenous newt LBCs; as expected, they stained
with antibodies against newt-specific proteins. Other heterologous
injections, including sperm heads of the frog Rana
pipiens and the zebrafish Danio rerio in
Xenopus GVs, confirm that LBCs can be derived from
taxonomically distant organisms. The GV system should help identify
both cis- and trans-acting factors needed to convert condensed
chromatin into transcriptionally active LBCs. It may also be useful in
producing cytologically analyzable chromosomes from organisms whose
oocytes do not go through a typical lampbrush phase or cannot be
manipulated by current techniques.
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