Meiosis in Schizophyllum commune: The effect of hydroxyurea on the frequency of recombination and mutations

Summary The effect of exposure of nuclei at different stages of meiosis to hydroxyurea (HU) was tested by examination of its effect on the frequency of auxotrophic mutations and on intergenic recombination. The results indicate that recombination is increased most significantly if the nuclei are exposed to the drug during the premeiotic-S phase and to a lesser extent if exposed during prophase. Similarly, nuclei exposed to HU during premeiotic-S phase and prophase mutate at a frequency 10 to 50 times higher than untreated meiotic nuclei. The degree of response of the mutagenic events and recombination events is not similar and it is suggested that the mutagenic events occur at stages prior to recombination. The temporal relations of the two events in response to HU suggest that the mutagenic events precede recombination and the results obtained with HU only amplify the mutagenic events that normally occur in meiotic nuclei and are related to the meiotic effect.     

Meiosis-activating sterols: background, discovery, and possible use

Several years ago we discovered that spent media from cultured human and bull testes contain components that initiate meiosis in germ cells from fetal mouse testes which have been cultured for 6 days in the spent medium. The active substance(s) was termed meiosis-inducing substance. We later found that human follicular fluid harvested after stimulation with gonadotropins has a similar effect. These meiosis-activating substances have now been identified and characterized in extracts from bull testes and human preovulatory follicular fluid as naturally occurring sterols (meiosis-activating sterols, MAS). MAS are intermediates in the cholesterol biosynthetic pathway and are thus present in all cells which produce cholesterol de novo and from lanosterol. However, MAS accumulate only in the gonads. We discuss the possible physiological role of these sterols in initiating meiosis and in oocyte resumption of meiosis, and their potential use in promoting and preventing fertility. Received: 2 December 1997*Accepted: 6 April 1998     

Effect of induced peritoneal endometriosis on oocyte and embryo quality in a mouse model

Purpose

To assess the impact of peritoneal endometriosis on oocyte and embryo quality in a mouse model.

Methods

Peritoneal endometriosis was surgically induced in 33 B6CBA/F1 female mice (endometriosis group, N = 17) and sham-operated were used as control (sham group, N = 16). Mice were superovulated 4 weeks after surgery and mated or not, to collect E0.5-embryos or MII-oocytes. Evaluation of oocyte and zygote quality was done by immunofluorescence under spinning disk confocal microscopy.

Results

Endometriosis-like lesions were observed in all mice of endometriosis group. In both groups, a similar mean number of MII oocytes per mouse was observed in non-mated mice (30.2 vs 32.6), with a lower proportion of normal oocytes in the endometriosis group (61 vs 83 %, p < 0.0001). Abnormalities were incomplete extrusion or division of the first polar body and spindle abnormalities. The mean number of zygotes per mouse was lower in the endometriosis group (21 vs 35.5, p = 0.02) without difference in embryo quality.

Conclusions

Our results support that induced peritoneal endometriosis in a mouse model is associated with a decrease in oocyte quality and embryo number. This experimental model allows further studies to understand mechanisms of endometriosis-associated infertility.     

Common genes and pathways in the regulation of the mitotic and meiotic cell cycles of Schizosaccharomyces pombe

Summary Cell division cycle mutants defective in G₁, DNA replication or nuclear division were tested for sporulation at semi-restrictive temperatures. In cdc1-7, cdc5-120, cdc17-L16 and cdc18-46 no abnormalities were observed; cdc10-129, cdc20-M10, cdc21-M6B, cdc23-M36 and cdc24-M38 formed four-spored asci but with a low efficiency; cdc22-M45 was completely defective in meiosis, but could conjugate and formed zygotes with a single nucleus. Mutants defective in the mitotic initiation genes cdc2, cdc25 and cdc13 were blocked in meiosis II. None of the wee1-50, adh.nim1 ⁺ and win1 ⁺ alleles had any affect on sporulation, suggesting that their interactions with cdc25 and cdc2 are specific to mitosis. The meiotic function of cdc13 is TBZ-sensitive and probably exerted downstream of cdc2. Single mutants in cut1 or cut2 did not effect sporulation, whereas the double mutant cut1 cut2 formed two-spored asci. The results demonstrate that the cell division cycle and the meiotic developmental pathway share common genes and regulatory cascades.     

直接低渗法制备男性不育症精液生精细胞染色体观察

目的：研究男性不育症生殖细胞减数分裂过程、生精细胞染色体畸变与不育的关系。方法：选择不育门诊中１９例男性原发不肓患者精液和４例禁欲期正常男性志愿者精液，应用直接低渗法，获得各级生精细胞（精原细胞、初级／次级精母细胞、精细胞）分裂相。结果：不同样本精液中各级生精细胞分裂相分布有极显著性差异（Ｐ〈０．００５）；弱精症患者精液标本中主要为ＭＩ单价体、染色单体畸变，少精症和无精症主要为联会消失、减数分裂阻断。结论：直接低渗法能为诊断男性不育提供有价值的细胞遗传学信息。生精细胞染色体畸变、减数分裂过程异常是导致男性不肓的原因之一。     

Meiotic double-strand breaks in Schizosaccharomyces pombe

Meiotic DNA double-strand breaks (DSBs) are associated with recombination hot spots in the yeast Saccharomyces cerevisiae and are believed to initiate the process of recombination. Until now, meiosis-induced breaks have not been shown to occur regularly in other organisms. Here we show, by pulsed-field gel electrophoresis of DNA, that meiotic DSBs occur transiently in all three chromosomes of the fission yeast Schizosaccharomyces pombe. In a repair defective mutant, carrying a mutation in the RecA homolog gene rhp51, meiotic DSBs accumulate. In contrast to expectation from the genetic map of S. pombe, however, many chromosomal DNA molecules remain unbroken during meiosis. Received: 27 February 2000 / 12 March 2000     

Evolutionary conservation of meiotic DSB proteins: more than just Spo11

Meiotic recombination is initiated by programmed DNA double-strand breaks (DSBs) generated by the Spo11 protein. In budding yeast, five other meiotic-specific proteins are also required for DSB formation, but, with rare exception, orthologs had not been identified in other species. In this issue of Genes & Development, Kumar and colleagues (pp. 1266–1280) used a phylogenomic approach to identify two of these proteins across multiple clades, and confirmed that one of these, MEI4, is a functional ortholog in mouse.     

An ameiotic mutant of Coprinus cinereus halted prior to pre-meiotic S-phase

Summary Five Coprinus cinereus monokaryons were isolated which bore a dominant mutation designated Mar. Dikaryons formed by mating Mar-bearing monokaryons with normal monokaryons produced aborted fruiting bodies in which the basidia never underwent karyogamy. The Mar mutation probably prevented pre-meiotic DNA replication; extracts of Mar-bearing dikaryons harvested at a stage equivalent to pre-meiotiv S-phase caused little net DNA synthesis in DNA polymerase assays. There was no marked incorporation of 32p into DNA (and low incorporation of 32p into RNA) of cap tissue from Mar-bearing fruiting bodies at a stage equivalent to pre-meiotic S-phase. The aborted fruiting bodies were similar to those resulting on normal cultures following treatment prior to S-phase with cycloheximide, or continuous light at 35 °C. In contrast to normal C. cinereus monokaryons, no Mar-bearing monokaryon formed fruiting bodies when subjected to nutritional stress.