TL;DR: It is observed that human DAZL (deleted in azoospermia-like) functions in primordial germ-cell formation, whereas closely related genes DAZ and BOULE promote later stages of meiosis and development of haploid gametes.
Abstract: The leading cause of infertility in men and women is quantitative and qualitative defects in human germ-cell (oocyte and sperm) development. Yet, it has not been possible to examine the unique developmental genetics of human germ-cell formation and differentiation owing to inaccessibility of germ cells during fetal development. Although several studies have shown that germ cells can be differentiated from mouse and human embryonic stem cells, human germ cells differentiated in these studies generally did not develop beyond the earliest stages. Here we used a germ-cell reporter to quantify and isolate primordial germ cells derived from both male and female human embryonic stem cells. By silencing and overexpressing genes that encode germ-cell-specific cytoplasmic RNA-binding proteins (not transcription factors), we modulated human germ-cell formation and developmental progression. We observed that human DAZL (deleted in azoospermia-like) functions in primordial germ-cell formation, whereas closely related genes DAZ and BOULE (also called BOLL) promote later stages of meiosis and development of haploid gametes. These results are significant to the generation of gametes for future basic science and potential clinical applications.
TL;DR: Results suggest that Xdazl may be important for primordial germ cell specification in the early embryo and may play a role analogous to Boule in promoting meiotic cell division.
Abstract: We have identified a localized RNA component of Xenopus germ plasm. This RNA, Xdazl (Xenopus DAZ-like), encodes a protein homologous to human DAZ (Deleted in Azoospermia), vertebrate DAZL and Drosophila Boule proteins. Human males deficient in DAZ have few or no sperm and boule mutant flies exhibit complete azoospermia and male sterility. Xdazl RNA was detected in the mitochondrial cloud and vegetal cortex of oocytes. In early embryos, the RNA was localized exclusively in the germ plasm. Consistent with other organisms, Xdazl RNA was also expressed in the spermatogonia and spermatocytes of frog testis. Proteins in the DAZ-family contain a conserved RNP domain implying an RNA-binding function. We have shown that Xdazl can function in vitro as an RNA-binding protein. To determine if the function of Xdazl in spermatogenesis was conserved, we introduced the Xdazl cDNA into boule flies. This resulted in rescue of the boule meiotic entry phenotype, including formation of spindles, phosphorylation of histone H3 and completion of meiotic cell division. Overall, these results suggest that Xdazl may be important for primordial germ cell specification in the early embryo and may play a role analogous to Boule in promoting meiotic cell division.
TL;DR: In this article, a Group III-V nitride boule is formed by growing a group III-v nitride material on a corresponding native Group III V nitride seed crystal by vapor phase epitaxy at a growth rate above 20 micrometers per hour.
Abstract: A boule formed by high rate vapor phase growth of Group III-V nitride boules (ingots) on native nitride seeds (Figure 1), from which wafers may be derived for fabrication of microelectronic structures (Figure 5). The boule is of microelectronic device quality, e.g., having a transverse dimension greater than 1 centimeter, a length greater than 1 millimeter, and a top surface defect density of less than 107 defects cm-2. The Group III-V nitride boule may be formed by growing a Group III-V nitride material on a corresponding native Group III-V nitride seed crystal by vapor phase epitaxy at a growth rate above 20 micrometers per hour.
Abstract: The first section of the chapter is concerned with the
membership of the boule - the conditions of appointment and
service, the men who served in the boule, and the rewards and
risks to which they were exposed. In particular the evidence
is surveyed for the allocation to individual demes of specified
numbers of seats in the boule, a system which seems in fact to
have broken down in the second century B.C., though it continued
to influence the layout of lists of bouleutae. The subdivision
of the boule into tribal prytanies is next examined, and it is
suggested that this may be the work of Ephialtes rather than a
part of Cleisthenes' original organisation. In connection with
the further subdivision of the prytanies so that some men should
always be on duty, attention is given to a recently advanced
theory that the prytanies split according to a regular scheme
resembling but not identical with Cleisthenes' division of the
tribes into trittyes: the evidence supports the adoption of such
a convention by some tribes, but not a universally enforced rule.
Little can be added to older discussions of the proedri, who took
over the presidential duties of the prytanes in the fourth
century, but their institution seems to be at any rate a little
later than the democratic restoration of 403/2. The chapter ends
with a study of the boule's meetings and meeting-places: the
buildings occupied by the boule in the Agora are discussed, with
special reference to the internal arrangements of the bouleuterium
and the conditions in which members of the public were admitted
during meetings; other places where the boule met are listed;
procedure at meetings is examined; and the evidence for the
position of the generals vis-a-vis the boule is reconsidered,
with the suggestion that except at the time of the Peloponnesian
War the generals did not in the classical period possess extra-
ordinary privileges.
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TL;DR: Heterologous expression of Twine rescues the boule meiotic-entry defect, indicating that the essential function of Boule at the transition from G2 to M phase during meiosis is in the control ofTwine translation.
Abstract: Boule, a Drosophila orthologue of the vertebrate Dazl fertility factors, is a testis-specific regulator of meiotic entry and germline differentiation. Mutations inactivating either Boule, which is an RNA-binding protein, or Twine, which is a Cdc25-type phosphatase, block meiotic entry in males. Here we show that twine and boule interact genetically. We also find that protein expression from twine messenger RNA correlates with cytoplasmic accumulation of Boule and is markedly reduced by boule mutations. Remarkably, heterologous expression of Twine rescues the boule meiotic-entry defect, indicating that the essential function of Boule at the transition from G2 to M phase during meiosis is in the control of Twine translation.