ABORTED GAMETOPHYTE 1 is required for gametogenesis in Arabidopsis

In flowering plants, the male and female gametogenesis is a crucial step of sexual reproduction. Although many genes have been identi fied as being involved in the gametogenesis process, the genetic mechanisms underlying gametogenesis remains poorly understood. We reported here characterization of the gene, ABORTED GAMETOPHYTE 1(AOG1) that is newly identi fied as essential for gametogenesis in Arabidopsis thaliana. AOG1 is expressed predominantly in reproductive tissues including the developing pollen grains and ovules. The AOG1 protein shares no signi ficant amino acid sequence similarity with other documented proteins and is located mainly in nuclei of the cells. Mutation in AOG1 caused degeneration of pollen at the uninucleate microspore stage and severe defect in embryo sacs, leading to a signi ficant reduction in male and female fertility.Furthermore, the molecular analyses showed that the aog1 mutant signi ficantly affected the expression of several genes, which are required for gametogenesis. Our results suggest that AOG1 plays important roles in gameto genesis at the stage prior to pollen mitosis I(PMI)in Arabidopsis, possibly through collaboration with other genes.     

Chromosomal Evidence on the Sporogony of Amblyospora californica (Microspora: Amblyosporidae) in Culex tarsalis (Diptera: Culicidae)

ABSTRACT. Amblyospora californica is a polymorphic, eukaryotic microsporidian. Three types of sporogony producing three types of spores occur in male larvae and female adults of its mosquito host, Culex tarsalis , and an alternate copepod host, Acanthocyclops vernalis. Development of A. californica in male larvae includes merogony and sporogony. Karyogamy and meiosis was observed in sporogony in male larvae but not in the female adult or in the copepod. Chromosomal evidence showed that sporogony included two consecutive meiotic divisions and a subsequent mitosis forming an octosporont, ultimately containing eight haploid, uninucleate mature spores. In this species, the haploid number of chromosomes is nine. Macrosporoblasts and macrospores, containing 1, 2 or more nuclei, can be seen in infected male larvae. The stage of sporogony in which cytokinesis was arrested seems to determine the number of nuclei. Those with only one nucleus, we believe are due to failed nuclear division at meiosis. Although A. californica displayed a process of karyogamy and meiosis similar to that of the species from Cx. salinarius , they may not be the same species because of the difference in their chromosome numbers.     

The ability of dehydrated hamster and human sperm nuclei to develop into pronuclei.

To determine whether the nuclei of mature mammalian spermatozoa are resistant to dehydrated conditions, nuclei of hamster and human spermatozoa were freeze-dried or treated with various dehydrating agents before injection into hamster oocytes. Freeze-dried nuclei remained capable of developing into pronuclei even after 12 mo of storage at 4 degrees C. The level of DNA synthetic activity in the sperm (male) pronucleus was comparable to that in the egg (female) pronucleus. Sperm nuclei that had been stored in 100% ethanol, 100% methanol, or chloroform-methanol (2:1) mixture for 20 days were also capable of developing into pronuclei. Even the nuclei that had been dehydrated ("fixed") with Carnoy's fluid could develop into morphologically normal pronuclei. However, the level of DNA synthesis in the pronuclei derived from these chemically dehydrated nuclei was generally lower than that in the female pronuclei. Although the genetic integrity of the dehydrated sperm nuclei is yet to be determined, nuclei of mature hamster and human spermatozoa appear to be fairly resistant to dehydrated conditions.     

Sporogenesis and Gametogenesis of Endangered Adenophora lobophylla Hong (Campanulaceae)

Reported in this paper are the microsporogenesis, megasporogenesis and the development of male and female gametophytes of the endangered species Adenophora lobophylla. The anther is four-sporangiate with its wall composed of four layers: epidermis, fibrous endothelium, middle layer and glandular tapetum of binucleate cells. The cytokinesis of microspore mother cell in meiosis is simultaneous, and tetrads are tetrahedral. Pollen grains are 2-celled at the dispersal stage. Ovule is anatropous, unitegmic and tenuinucellate with a hypodermal archesporial cell developing directly as the megaspore mother cell which undergoes meiotic division and then forms a linear tetrad. The embryo sac is of Polygonum type. The polar nuclei fuse before fertilization. An endothelium differentiates when the uninucleate embryo sac forms. Comparative studies were made with the closely related and widely distributed species A. potaninii. No differences between them were found. No obstacle to sexual reproduction in this endangered species was observed. As a conclusion, no endangering factors were found to influence the sporogenesis and gametogenesis of A. lobophylla. According to our observision and the references on embryological studies of the Campanulaceae(s. l. ), there is no evident differentiation in sporogenesis and gametogenesis in this family.     

Preferential digestion of chloroplast DNA in male gametangia during the late stage of gametogenesis in the anisogamous algaBryopsis maxima

Summary The fate of chloroplast nuclei (cp-nuclei) and mitochondrial nuclei (mt-nuclei) was followed during gametogenesis in male and female coenocytic thalli in the anisogamous algaBryopsis maxima by epifluorescence microscopy, after staining with 4,6-diamidino-2-phenylindole (DAPI), by quantification of chloroplast DNA (cp-DNA) by fluorimetry using a video-intensified, photon-counting system (VIMPICS), and by CsCl density gradient centrifugation. The male and female coenocytic thalli, 48 h before the release of gametes, contain a large number of chloroplasts, each of which is larger in size than the cell nucleus and the mitochondria and contains about 150 cp-nuclei. The size of each chloroplast in the female and male gametangia decreases markedly during gametogenesis as a result of continuous divisions till about 10 h before the release of gametes and, eventually, the numbers of cp-nuclei per chloroplast in the male and female gametangia fall to about 20 and 5, respectively. Two hours later, as the preferential digestion of cp-DNA in the male gametangium occurs, the number of cp-nuclei in the chloroplast of each male gamete falls to zero while the number of cp-nuclei in female gamete does not change, even after release of female gametes. Several mt-nuclei are observed in all of the female gametes. By contrast, the mt-nuclei in the bulk of the male gametes disappear but those in a few gametes remain. The profiles after CsCl density gradient centrifugation of DNAs extracted from male and female plants and gametes support the cytological data. The results suggest that the preferential digestion of cp-DNA in male plants occurs about 8 h before the release of gametes and that there is differential digestion of cp-DNA and mitochondrial DNA (mt-DNA).     

濒危植物裂叶沙参的大小孢子发生及雌雄配子体发育

本文以近缘广布种泡沙参为对照,对濒危物种裂叶沙参进行了大小孢子发生和雌雄配子体发育的研究。裂叶沙参的药壁发育为双子叶型,绒毡层为腺质型,细胞含两核。小孢子母细胞在减数分裂过程中胞质分裂为同时型。小孢子四分体为四面体型,成熟花粉粒为2-细胞型。胚珠倒生,单珠被,薄珠心,大孢子四分体为线形排列,胚囊发育为蓼型。成熟胚囊中两极核在受精之前融合为一个大的次生核。当胚囊发育至单核胚囊时,珠被的最内层细胞发育为珠被绒毡层。濒危植物裂叶沙参在大、小孢子发生及雌、雄配子体的发育过程中,未见有败育及其它异常现象;与对照种泡沙参相比,也未见有差异,这说明裂叶沙参的致濒原因不在于有性生殖过程。     

FINE STRUCTURE OF THE MALE AND FEMALE GAMETES OF ATRACTOMORPHA PORCATA (SPHAEROPLEACFAE,CHLOROPHYTA) WITH EMPHASIS ON THE DEVELOPMENT AND ABSOLUTE CONFIGURATION OF THE FLAGELLAR APPARATUS1

Gametogenesis in Atractomorpha porcata Hoffman was initiated b the synchronous mitotic division of nuclei within a multinucleate gametangium. Uninucleate gametes were subsequently produced following two series of cytokinetic divisions. The first series involved the formation of phycoplast microtubules (phycoplastic cytokinesis), whereas the second series did not (nonphycoplastic cytokinesis). Centrioles were connected by a rudimentary striated distal fiber by the time they migrated to the planes of division preceding the first series of cytokinetic division. These first divisions produced binucleate gametocytes. A well-developed flagellar apparatus lay near the cell surface in close proximity to each nucleus of the gametocyte prior to the second series of cytokinetic divisions that produced the uninucleate gametes. As seen in apical view, the paired basal bodies were directly opposed, with no lateral displacement of their longitudinal axes. In lateral view, the paired basal bodies diverged from one another at an angle of 130–180° (female) or 170–180° (male) and were connected by an arched, distal striated fiber about 670–750 nm long and 600 nm at its widest part. Four electron-opaque, pyramid-shaped lateral bodies flanked the basal bodies in close contact with their undersurfaces. The flagellar roots demonstrated a cruciate arrangement, with s = 6–9 over 1 (female gametes) or 7–10 over 1 (male gametes) microtubules and d= 2 microtubules. In male gametes, one of the multistranded roots was located close to the eyespot, and a second system of cytoskeletal microtubules was detected internally. Based on gamete ultrastructure, Atractomorpha porcata appears to be the most undifferentiated member of the genus.     

The cytology of paedogenesis in the gall midgeMycophila speyeri

In paedogenetically developing female eggs of the gall midgeMycophila speyeri only one equational meiotic division occurs. The primary cleavage nucleus contains 29 chromosomes. In the fourth cleavage division 23 chromosomes are eliminated from the future somatic nuclei while the primordial germ-line nucleus keeps the high chromosome number.—The paedogenetic development of male eggs begins with two meiotic divisions. The egg nucleus with 14 or 15 chromosomes fuses with two, sometimes only one, somatic nuclei (2n=6) of maternal origin (regulation). Thus the primary cleavage nucleus contains 26 or 27 chromosomes, sometimes only 20 or 21. Elimination in cleavage divisions V and VI leeds to somatic nuclei with 3 chromosomes while the primordial germ-line nucleus keeps the high chromosome number.—Differences between male and female eggs and the evolution of regulation in gall midges are discussed.     

Parasexually produced hybrids between female and male plants of Griffithsia tenuis C. Agardh,a red alga

Somatic cell fusion between vegetative cells of a male and a female isolate of Griffithsia tenuis, a marine red alga, has been obtained. Hybrid cells have been isolated and they have regenerated new plants. Almost all these hybrid plants made reproductive structures. In nearly half these cases the first 3–10 cells of the hybrid filament produced reproductive structures chracteristic of the tetrasporic (diploid) phase rather than the sexual (haploid) phase of the life cycle of this alga. However as these filaments continued to grow, cells further along the filament began to produce sexual, either female or male, reproductive structures. The observations suggest that the production of tetrasporangial branches does not require the fusion of male and female nucleic; rather, male and female nucleic remaining separate, act in concert to produce these structures, and in subsequent cell divisions the nuclei of one sex may be left behind allowing the nuclei of the remaining sex to direct the production of sexual branches.     

Haploid maternal genome derived from early diplotene oocytes can substitute for the female pronucleus in preimplantation mouse development

We describe the preimplantation development of mouse embryos that have received the haploid maternal genome derived from early diplotene nuclei of primordial oocytes (PO). Two generations of recipient egg-cells were used. Induction of two meiotic divisions of the PO nucleus and the reduction of the number of chromosomes to the haploid level were achieved in preovulatory oocytes (primary recipients). The developmental potential of the obtained haploid genome was examined in zygotes (secondary recipients). The nuclei of PO obtained from newborn mice were transferred by cell electrofusion to in vitro maturing (IVM) and enucleated preovulatory mouse oocytes. The reconstructed oocytes which had completed maturation, i.e., reached metaphase II, were artificially activated (8% ethanol + CHX). Activated oocytes were used as donors of haploid pronuclei of PO origin which were transferred (by karyoplast fusion) to partially enucleated zygotes containing only the male pronucleus. Thus, reconstituted zygotes were transplanted to the ligated oviducts of the cycling mice and 27% of them developed to the blastocyst stage. Our experiments demonstrate that 1) the nucleus of PO can be induced to premature meiotic divisions in an IVM enucleated preovulatory oocyte; 2) in the presence of a normal male pronucleus, the haploid pronucleus of PO origin can substitute for a female pronucleus during preimplantation development. Mol. Reprod. Dev. 48:488–495, 1997. © 1997 Wiley-Liss, Inc.     

Male germ line,spermatogenesis and karyotypes of Heteropeza pygmaea winnertz (Diptera: Cecidomyiidae)

The germ line during the development of the male of the gall midge Heteropeza pygmaea was followed cell generation by cell generation. The development of the male egg begins with two meiotic divisions, followed by fusion of one of the resulting nuclei with (usually) two somatic nuclei (regulation), after which the regulated nucleus passes through 9–10 mitoses, and finally a further two meiotic divisions producing the spermatids. The chromosome numbers (determined by colchicine and air-drying techniques) of the race studied are 55 in the female germ line, very variable with a mean near 47–48 in the male germ line after regulation, 5 or 6 in the sperms, 10 in the female somatic nuclei and 5 in the male somatic nuclei. Statistical techniques for analysis of the different karyotypes are developed and a model explaining the known cytological events in Heteropeza is presented.     

Nuclear envelope breakdown is under nuclear not cytoplasmic control in sea urchin zygotes

Nuclear envelope breakdown (NEB) and entry into mitosis are though to be driven by the activation of the p34cdc2-cyclin B kinase complex or mitosis promoting factor (MPF). Checkpoint control mechanisms that monitor essential preparatory events for mitosis, such as DNA replication, are thought to prevent entry into mitosis by downregulating MPF activation until these events are completed. Thus, we were surprised to find that when pronuclear fusion in sea urchin zygotes is blocked with Colcemid, the female pronucleus consistently breaks down before the male pronucleus. This is not due to regional differences in the time of MPF activation, because pronuclei touching each other break down asynchronously to the same extent. To test whether NEB is controlled at the nuclear or cytoplasmic level, we activated the checkpoint for the completion of DNA synthesis separately in female and male pronuclei by treating either eggs or sperm before fertilization with psoralen to covalently cross-link base-paired strands of DNA. When only the maternal DNA is cross-linked, the male pronucleus breaks down first. When the sperm DNA is cross-linked, male pronuclear breakdown is substantially delayed relative to female pronuclear breakdown and sometimes does not occur. Inactivation of the Colcemid after female NEB in such zygotes with touching pronuclei yields a functional spindle composed of maternal chromosomes and paternal centrosomes. The intact male pronucleus remains located at one aster throughout mitosis. In other experiments, when psoralen-treated sperm nuclei, over 90% of the zygote nuclei do not break down for at least 2 h after the controls even though H1 histone kinase activity gradually rises close to, or higher than, control mitotic levels. The same is true for normal zygotes treated with aphidicolin to block DNA synthesis. From these results, we conclude that NEB in sea urchin zygotes is controlled at the nuclear, not cytoplasmic, level, and that mitotic levels of cytoplasmic MPF activity are not sufficient to drive NEB for a nucleus that is under checkpoint control. Our results also demonstrate that the checkpoint for the completion of DNA synthesis inhibits NEB by acting primarily within the nucleus, not by downregulating the activity of cytoplasmic MPF.     

Patterns of genetic mosaicism in the antennae and legs of Habrobracon juglandis

Habrobracon females which are homozygous for the mutant ebony produce a high frequency of mosaics in their progeny. This is probably due to a delay in the migration of pronuclei, which may result in a prefertilization cleavage of one or both of them. The mosaics are zygogenetic-androgenetic, zygogenetic-gynogenetic, or gynogenetic-androgenetic in origin. The distribution of phenotypes in the adult mosaics is nonrandom, probably corresponding to the original relative positions of the pronuclei. Mosaicism patterns were studied in the legs and antennae, both of which show longitudinal clonal patterns presumably resulting from oriented cell divisions during development. Mosaicism frequencies for the appendages are similar to those found in Drosophila, indicating that the imaginal discs are initiated as similar-sized groups of cells in the two insects. The Habrobracon antenna shows sexual dimorphism, containing 19 flagellar segments in the male and 12 in the female. Gynandromorphic antennae contain male, female and mixed segments, but female segments are never found distal to the twelfth segment. The gynandromorphic antennae show a high frequency of incomplete or helical segments, occurring most frequently in segments 10–13. The data are discussed in relation to the problem of appendage segmentation.     

Gametogenesis in the cirratulid polychaetes Dodecaceria concharum and D. caulleryi

In Northumberland Dodecaceria concharum coexists in the same habitat as D. caulleryi . Morphologically both species are very similar but reproductively they are not. D. concharum is a parthenogenetic atoke while D. caulleryi has an asexual cycle that ends in an epitokous sexual phase. Histologically the gonad of both species had six cell types and the number of cells in each type were found during gametogenesis. In D. concharum the period over which gametogenesis occurs was followed from the increase in size of free coelomic oocytes and numbers of body segments. In D. caulleryi the period was followed by means of changes in the asexual cycle and metamorphosis into epitokes. In spite of the differences in the methods of reproduction of the two species gametogenesis of each was found to be almost identical. Only oogenesis could be compared since D. concharum does not have males. Prior to spawning in both species the production of oocytes by the ovary appeared to be inhibited. Possible hormonal mechanisms used to control atokous and epitokous spawning are discussed. From the histology of the gonads and oocytes D. concharum appeared to have half the number of chromosomes of D. caulleryi.     

Full-term development of mouse eggs transplanted with male pronuclei derived from round spermatids: the effect of synchronization between male and female pronucleus on embryonic development

Pronucleus transplanted mice have been produced, but their donor male pronuclei were derived from mature sperm and were completely synchronous with female pronuclei because both male and female pronuclei came from the same fertilized oocyte. The present study firstly produced male pronuclei by introducing round spermatids into enucleated mouse oocytes, then transferred the male pronuclei into mouse oocytes at three activation stages and finally compared the effect of three kinds of oocytes on the development of reconstructed embryos. Our results indicate that, in enucleated oocytes, mouse round spermatid nuclei can transform to male pronuclei in a higher proportion, and the synchronization between male and female pronucleus does not significantly influence the early cleavage but the later and full-term development of reconstructed embryos.     

Effect of egg composition on the developmental capacity of androgenetic mouse embryos.

Analysis of the developmental capacities of androgenetic and gynogenetic mouse embryos (bearing two paternal or two maternal pronuclei, respectively) revealed a defect in blastocyst formation of androgenetic, but not gynogenetic, embryos that was a function of the maternal genotype. Androgenetic embryos constructed using fertilized eggs from C57BL/6 or (B6D2)F1 mice developed to the blastocyst stage at frequencies similar to those previously reported, whereas androgenetic embryos constructed with fertilized eggs from DBA/2 mice developed poorly, the majority failing to progress beyond the 16-cell stage and unable to form a blastocoel-like cavity, regardless of whether the male pronuclei were of C57BL6 or DBA/2 origin. This impaired development was observed even in androgenetic embryos constructed by transplanting two male pronuclei from fertilized DBA/2 eggs to enucleated C57BL/6 eggs, indicating that the defect cannot be explained as the lack of some essential component in the DBA/2 cytoplasm that might otherwise compensate for androgeny. Rather, the DBA/2 egg cytoplasm apparently modifies the incoming male pronuclei differently than does C57BL/6 egg cytoplasm. Several specific alterations in the protein synthesis pattern of DBA/2 androgenones were observed that reflect a defect in the regulatory mechanisms that normally modulate the synthesis of these proteins between the 8-cell and blastocyst stages. These results are consistent with a model in which cytoplasmic factors present in the egg direct a strain-dependent modification of paternal genome function in response to epigenetic modifications (genomic imprinting) established during gametogenesis and indicate that preimplantation development can be affected by these modifications at both the morphological and biochemical levels.     

Ultrastructural Study and Description of Ovavesicula popilliae N. G., N. Sp. (Microsporida: Pleistophoridae) from the Japanese Beetle,Popillia japonica (Coleoptera: Scarabaeidae)1

A new genus and species of microsporidia, Ovavesicula popilliae n. g., n. sp., is described from the Japanese beetle, Popillia japonica, on the basis of studies by light and electron microscopy. Parasite development primarily occurs within the Malpighian tubules of larvae, and spores are formed in a sporophorous vesicle. Meronts have diplokaryotic nuclei, develop in direct contact with the host cell cytoplasm, and divide by binary fission. Sporonts have unpaired nuclei, develop within a thick sporophorous vesicle, and undergo synchronous nuclear divisions producing plasmodia with 2, 4, 8, 16, and 32 nuclei. Cytokinesis of sporogonial plasmodia does not occur until karyokinesis is complete with 32 nuclei. Intact sporophorous vesicles are ovoid, containing numerous secretory products, and are surrounded by a persistent two-layered wall. The uninucleate spores are regularly formed in groups of 32, and the polar tube in each has six coils.