DIFFERENTIAL BINDING OF OOCYTE-TYPE AND SOMATIC-TYPE 5S RIBOSOMAL-RNATO TFIIIA AND RIBOSOMAL-PROTEIN L5 IN XENOPUS OOCYTES - SPECIALIZATION FOR STORAGE VERSUS MOBILIZATION
La. Allison et al., DIFFERENTIAL BINDING OF OOCYTE-TYPE AND SOMATIC-TYPE 5S RIBOSOMAL-RNATO TFIIIA AND RIBOSOMAL-PROTEIN L5 IN XENOPUS OOCYTES - SPECIALIZATION FOR STORAGE VERSUS MOBILIZATION, Developmental biology, 168(2), 1995, pp. 284-295
We studied the pathway of 5S ribosomal RNA (rRNA) during oogenesis in
Xenopus from its storage in the cytoplasm to incorporation into riboso
mes in the nucleus. Ribonucleoprotein particle (RNP) assembly assays r
eveal striking differences in the behavior of oocyte-type and somatic-
type 5S rRNA after microinjection into stage II, III, or IV oocytes or
into the cytoplasm of stage V-VI oocytes. Microinjected oocyte-type 5
S rRNA predominantly interacts with the 5S rRNA gene-specific transcri
ption factor IIIA (TFIIIA) to form storage 75 RNPs. In contrast, micro
injected somatic-type 5S rRNA predominantly interacts with ribosomal p
rotein L5 to form 5S RNPs, which are precursors to ribosome assembly.
In addition, a greater amount of somatic-type 5S rRNA accumulates in t
he nucleus and is assembled into 60S ribosomal subunits. Thus, a sligh
t difference in nucleotide sequence results in differential binding of
5S rRNA to TFIIIA and L5, specializing oocyte-type for storage in the
oocyte cytoplasm and somatic-type for rapid mobilization and ribosome
assembly. When oocyte-type and somatic-type 5S rRNA molecules were mi
croinjected into the nucleus of stage V-VI oocytes in excess of other
ribosomal components, the nucleocytoplasmic distribution of both types
of RNA was similar, but the distinctive protein associations were mai
ntained. In contrast, the behavior of oocyte-type and somatic-type 5S
rRNA gradually synthesized in situ from microinjected cloned genes was
similar, suggesting that nascent RNA is rapidly and directly recruite
d into ribosomes, thus bypassing an excursion into the cytoplasm prior
to ribosome assembly. (C) 1995 Academic Press, Inc.