scholarly journals Paternal Chromosome Incorporation into the Zygote Nucleus Is Controlled by maternal haploid in Drosophila

2001 ◽  
Vol 231 (2) ◽  
pp. 383-396 ◽  
Author(s):  
Benjamin Loppin ◽  
Frédéric Berger ◽  
Pierre Couble

Development ◽  
2001 ◽  
Vol 128 (19) ◽  
pp. 3809-3817 ◽  
Author(s):  
Silvia Bongiorni ◽  
Milena Mazzuoli ◽  
Stefania Masci ◽  
Giorgio Prantera

The behavior of chromosomes during development of the mealybug Planococcus citri provides one of the most dramatic examples of facultative heterochromatization. In male embryos, the entire haploid paternal chromosome set becomes heterochromatic at mid-cleavage. Male mealybugs are thus functionally haploid, owing to heterochromatization (parahaploidy). To understand the mechanisms underlying facultative heterochromatization in male mealybugs, we have investigated the possible involvement of an HP-1-like protein in this process. HP-1 is a conserved, nonhistone chromosomal protein with a proposed role in heterochromatinization in other species. It was first identified in Drosophila melanogaster as a protein enriched in the constitutive heterochromatin of polytene chromosome. Using a monoclonal antibody raised against the Drosophila HP-1 in immunoblot and immunocytological experiments, we provide evidence for the presence of an HP-1-like in Planococcus citri males and females. In males, the HP-1-like protein is preferentially associated with the male-specific heterochromatin. In the developing male embryos, its appearance precedes the onset of heterochromatization. In females, the HP-1-like protein displays a scattered but reproducible localization pattern along chromosomes. The results indicate a role for an HP-1-like protein in the facultative heterochromatization process.



Development ◽  
1988 ◽  
Vol 102 (2) ◽  
pp. 287-299 ◽  
Author(s):  
R.R. Franks ◽  
B.R. Hough-Evans ◽  
R.J. Britten ◽  
E.H. Davidson

A method is described for microinjection of cloned DNA into the zygote nucleus of Lytechinus variegatus. Eggs of this species are unusually transparent, facilitating visual monitoring of the injection process. The initial fate of injected DNA fragments appears similar to that observed earlier for exogenous DNA injected into unfertilized egg cytoplasm. Thus after end-to-end ligation, it is replicated after a lag of several hours to an extent indicating that it probably participates in most of the later rounds of DNA synthesis undergone by the host cell genomes during cleavage. The different consequences of nuclear versus cytoplasmic injection are evident at advanced larval stages. Larvae descendant from eggs in which exogenous DNA was injected into the nuclei are four times more likely (32% versus 8%) to retain this DNA in cell lineages that replicate very extensively during larval growth, i.e. the lineages contributing to the imaginal rudiment, and thus to display greatly enhanced contents of the exogenous DNA. Similarly, 36% of postmetamorphic juveniles from a nuclear injection sample retained the exogenous DNA sequences, compared to 12% of juveniles from a cytoplasmic injection sample. However, the number of copies of the exogenous DNA sequences retained per average genome in postmetamorphic juveniles was usually less than 0.1 (range 0.05-50), and genome blot hybridizations indicate that these sequences are organized as integrated, randomly oriented, end-to-end molecular concatenates. It follows that only a small fraction of the cells of the average juvenile usually retains the exogenous sequences. Thus, even when introduced by nuclear microinjection, the stable incorporation of exogenous DNA in the embryo occurs in a mosaic fashion, although in many recipients the DNA enters a wider range of cell lineages than is typical after cytoplasmic injection. Nuclear injection would probably be the route of choice for studies of exogenous DNA function in the postembryonic larval rudiment.



Development ◽  
1971 ◽  
Vol 25 (3) ◽  
pp. 277-299
Author(s):  
S. K. Moloo

The degree of determination of the young embryo of S. gregaria has been investigated using ligation, thermocautery and centrifugation techniques. From the overall results, it is suggested that the early development of the embryo is mediated by two physiological centres. The formation of the germ rudiment is controlled by an activation centre located in the periplasm round the posterior end of the egg. This centre is already present at the zygote nucleus stage and is essential during the very early cleavage period. The differentiation of the germ band is induced by the activity of a second centre, the differentiation centre, located in the presumptive thorax. It apparently becomes established at least by the late blastoderm stage and its activity continues during the period of germ-band formation. During the late cleavage and early blastoderm stages, the egg is labile and the embryo is therefore able to normalize its development after part or parts of the germinal Anlage have been cauterized, removed or displaced. The differentiation centre completes its functions by the beginning of gastrulation. Thereafter, the embryo is determined. The embryo can regulate its size at least up to the gastrulation stage provided that a certain minimum amount of usable yolk is available. The development of the serosa is not under the control of either centre. This structure seems to be capable of regeneration providing that a part of the extra-embryonic blastoderm remains intact.



1968 ◽  
Vol 16 (1) ◽  
pp. 101 ◽  
Author(s):  
MJD White

An individual of the large grasshopper Valanga irregularis (Walker) which exhibited bilateral gynandromorphism, is described. The entire right side was female, the left side being male. The colour pattern on the two sides was completely different, the male side corresponding to the concolorous phenotype, the female side to the contrasty one. The gonad was an undeveloped ovotestis, the testicular part being XO (2n = 23). There are two obvious explanations of this gynandromorph: (1) that a single XX zygote nucleus gave rise to XX and XO nuclei through loss of an X; in this case we would be dealing with a sex-linked pattern polymorphism, the gene for the contrasty morph being dominant to the concolorous allele; (2) that the gynandromorph arose from a binucleate egg, as a result of double fertilization. Data on the frequency of the morphs in the two sexes, in natural populations, do not support the first hypothesis, and it is concluded that the second one must be correct.





2016 ◽  
Vol 16 (3-4) ◽  
pp. 116-119
Author(s):  
Udayakumar Narasimhan ◽  
Vidya Krishna ◽  
Shruthi Mohan ◽  
Solomon F.D. Paul ◽  
Teena Koshy


1991 ◽  
Vol 114 (5) ◽  
pp. 929-940 ◽  
Author(s):  
M Terasaki ◽  
L A Jaffe

The ER of eggs of the sea urchin Lytechinus pictus was stained by microinjecting a saturated solution of the fluorescent dicarbocyanine DiIC18(3) (DiI) in soybean oil; the dye spread from the oil drop into ER membranes throughout the egg but not into other organelles. Confocal microscopy revealed large cisternae extending throughout the interior of the egg and a tubular membrane network at the cortex. Since diffusion of DiI is confined to continuous bilayers, the spread of the dye supports the concept that the ER is a cell-wide, interconnected compartment. In time lapse observations, the internal cisternae were seen to be in continuous motion, while the cortical ER was stationary. After fertilization, the internal ER appeared to become more finely divided, beginning as a wave apparently coincident with the calcium wave and becoming most marked by 2-3 min. By 5-8 min the ER returned to an organization similar to that of the unfertilized egg. The cortical network also changed at fertilization; it became disrupted and eventually recovered. DiI labeling allowed continuous observations of the ER during pronuclear migration and mitosis. DiI-stained membranes accumulated in the region of the microtubule array surrounding the sperm nucleus and centriole (the sperm aster) as it migrated to the center of the egg; this accumulation persisted near the centrosomes and zygote nucleus throughout pronuclear fusion and the first two mitotic cycles. We have used a new method to observe the spatial and temporal organization of the ER in a living cell, and we have demonstrated a striking reorganization of the ER at fertilization.



2015 ◽  
Vol 16 (1) ◽  
Author(s):  
Stefano Stagi ◽  
Elisabetta Lapi ◽  
Marilena Pantaleo ◽  
Massimo Carella ◽  
Antonio Petracca ◽  
...  


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