Desynapsis and spontaneous trisomy in jute (Corchorus olitorius L.)

Summary Cytological studies in desynaptic plants, isolated at the F₆ generation of an intervarietal cross of Corchorus olitorius L., have shown variable numbers of bivalents and univalents in the PMC's at metaphase I, resulting in irregular distribution of chromosomes at anaphase I. The progenies of the desynaptic plants consisted of 9.24 percent of all possible primary trisomies except trisomie 6. The desynaptic condition is controlled by a pair of simple recessive genes.     

Chromosome-specific desynapsis in the n = 2 race of Haplopappus gracilis (Compositae)

During cytological screening for pollen sterility in a wild population of Haplopappus gracilis (n = 2), several partially sterile plants were found that had good pachytene pairing but varying numbers of univalents. Some plants had chromosome A bivalents or A univalents, while in the same cells chromosome B had only bivalents. In other plants the reverse condition occurred; the B chromosome had B bivalents or B univalents and only A bivalents. This demonstrates a chromosome-specific effect for the desynapsis genes. Hybridization between the two homozygous mutant genotypes produced only normal bivalents; this indicates the two mutants are not alleles and each is recessive. An F2 generation showed independent assortment of the desynaptic mutations. The chromosome A bivalent is the larger of the two and normally has one or two chiasmata; the B bivalent normally has a single chiasma. Chiasmata distribution was tested in the desynaptic mutant A bivalents and showed an acceptable fit to a binomial distribution. This occurs also in heterozygous, asynaptic pairing control gene mutations. Analysis of the NOR bivalent in two hologenomic desynaptic mutations in tomato also showed a good fit to a binomial distribution of chiasmata. This indicates the same methods are applicable to diverse species.     

The dsy10 Mutation of Arabidopsis results in desynapsis and a general breakdown in meiosis

The proper pairing and recombination of chromosomes during prophase is essential for the formation of gametes during meiosis. As part of studies to identify genes required for homologous chromosome pairing and recombination during meiosis in plants, we characterized a number of T-DNA-tagged, male-sterile mutants of Arabidopsis. Preliminary cytological studies on one line, 7219 which is male and female sterile, suggested that the mutation may disrupt meiosis and result in the formation of aberrant microsporocytes and microspores. In this report we present the results of a detailed analysis of meiosis in microsporocytes of sterile plants to elucidate the nature of the 7219 mutation. Analysis indicates that the mutation usually results in a desynaptic phenotype, with ten sister chromatids observed prior to metaphase I in most cells. Based on this, we named the mutation dsy10. The presence of several other meiotic defects suggests that dsy10 may not be a typical desynaptic mutant. Received: 15 December 2000 / Accepted: 19 April 2001     

4个春性基因型小麦品种与‘京841’杂交F_1代的表型分析

选用4个具有不同显性春化基因型的小麦品种与冬性小麦品种‘京841’进行杂交实验,通过显性春化基因特异性PCR分析技术鉴定杂交F1代植株,并分析4个杂交组合的正反交F1代植株表型特性。结果显示,各显性春化基因已经导入到各杂交F1代植株中,且其苗穗期受显性春化基因的控制而有效缩短;3个杂交组合的F1代穗粒数在正反交之间存在显著差异,推测穗粒数受细胞质遗传因素的影响较大,其中以‘新春2号’和‘豫麦18’分别为母本和父本与‘京841’杂交后F1代的穗粒数表现出较强的杂种优势,4个杂交组合的F1代千粒重均表现出较强的杂种优势。     

一种联会消失突变水稻的发现及其细胞学研究

从品种轮回４２２的群体中发现一不育单株,经细胞学观察证明是发生了消失突变,由于该植株的花粉母细胞在减数分裂终变期晚期平均有８．６９个二价体发生了消失,占二价体总数的７２．４％,发生联会消失的最多二价体数目为１２,根据联会消失的最多价体数目以及单位细胞的二价体频率,确定该联合消失变异为完全联会消失变异。     

Expression and inheritance of a desynaptic phenotype with impaired homologous synapsis in rye

The cytological phenotype was studied in a desynaptic form isolated from a population of rye cultivar Vyatka. The primary defect of desynaptic plants was identified as nonhomologous (heterologous) chromosome synapsis, which was observed by electron microscopy of synaptonemal complexes (SCs) in meiotic prophase I. Synapsis defects involved switches of synapsing axial elements to nonhomologous partners, asynapsis in the switching region, and foldbacks formed by the SC lateral elements. Defective bivalent formation was observed at later stages: the univalent number varied and multivalent chromosome associations were observed in single cells in metaphase I. The desynaptic phenotype was controlled by two recessive genes, sy8a and sy8b, which acted and were inherited independently. In a hybrid combination with line Ku-2/63, the desynaptic phenotype was suppressed by the dominant allele of a third gene for inhibitor I; the segregation in hybrid families corresponded to 57:7.     

Expression and Inheritance of a desynaptic phenotype with impaired homologous synapsis in rye

The cytological phenotype was studied in a desynaptic form isolated from a population of rye cultivar Vyatka. The primary defect of desynaptic plants was identified as nonhomologous (heterologous) chromosome synapsis, which was observed by electron microscopy of synaptonemal complexes (SCs) in meiotic prophase I. Synapsis defects involved switches of synapsing axial elements to nonhomologous partners, asynapsis in the switching region, and foldbacks formed by the SC lateral elements. Defective bivalent formation was observed at later stages: the univalent number varied and multivalent chromosome associations were observed in single cells in metaphase I. The desynaptic phenotype was controlled by two recessive genes, sy8a and sy8b, which acted and were inherited independently. In a hybrid combination with line Ku-2/63, the desynaptic phenotype was suppressed by the dominant allele of a third gene for inhibitor I; the segregation in hybrid families corresponded to 57:7.     

Cytogenetic behaviour and phosphate and potassium content in desynaptic pearl millet

Summary Continued inbreeding by self pollination resulted in a proportion of sterile plants in some families of the inbred line IP 1475 of Pennisetum americanum (L.) Leeke. Cytological examinations of the sterile plants revealed mild to extreme desynapsis and also chromosome fragmentation in some plants. Segregation ratios in the selfed families did not fit into any simple Mendelian ratio; however, in one F₂ family of the cross desynaptic x normal, segregation into 15 normal: 1 desynaptic was observed. Plants from a segregating family were classified as normals, desynaptics with 2–6 univalents, desynaptics with 2–10 univalents, desynaptics with 10–14 univalents and desynaptics with chromosome fragmentation. Estimation of the content of phosphate and potassium from the flag leaves did not reveal significant differences between the five groups of plants.     

Cytogenetic Analysis of Cotton Monosomics

Eleven monosomics in cotton that were obtained in the progenies of three disomic desynaptic plants were cytologically characterized. The transmission of the monosomes in progeny was shown in the 26 monosomic plants. In 23 plants the frequency of monosomics was ranged between 14.29 and 41.67 %. Three monosomics usually occurred in much lower frequencies (from 3.03 to 5.00 %). Various transmission rates indirectly pointed out different monosomes as a specific chromosomes of cotton genome. Three telochromosomes and one isochromosome were isolated from the progenies of the four monosomics. Using translocation test it was recovered that seven monosomes of different monosomics are homologous to one of the chromosomes of six translocation lines of our collection.     

Desynapsis in diploid and tetraploid clones of ryegrass

Desynapsis is described in diploid and tetraploid plants of perennial ryegrass. The plants were derived by repeated cloning of a single mixoploid (2n=14 and 28) detected among colchicine-treated seedlings. The diploid and tetraploid clones varied in degree of desynapsis, chiasma number, and fertility. The variation among the clones was probably environmental. The progeny of the mixoploid parent included dipoids, tetraploids, and an aneuploid. One diploid and the aneuploid were desynaptic and originated perhaps by selfing. Apparently a single recessive gene determined desynapsis. The role of synaptic genes in controlling the chemical structure and function of nucleoprotein macromolecules is discussed.     

A puromycin-sensitive aminopeptidase is essential for meiosis in Arabidopsis thaliana

Puromycin-sensitive aminopeptidases (PSAs) participate in a variety of proteolytic events essential for cell growth and viability, and in fertility in a broad range of organisms. We have identified and characterized an Arabidopsis thaliana mutant (mpa1) from a pool of T-DNA tagged lines that lacks PSA activity. This line exhibits reduced fertility, producing shorter siliques (fruits) bearing a lower number of seeds compared with wild-type plants. Cytogenetic characterization of meiosis in the mutant line reveals that both male and female meiosis are defective. In mpa1, early prophase I appears normal, but after pachytene most of the homologous chromosomes are desynaptic, thus, by metaphase I a high level of univalence is observed subsequently leading to abnormal chromosome segregation. Wild-type plants treated with specific inhibitors of PSA show a very similar desynaptic phenotype to that of the mutant line. A fluorescent PSA-specific bioprobe, DAMPAQ-22, reveals that the protein is maximally expressed in wild-type meiocytes during prophase I and is absent in mpa1. Immunolocalization of meiotic proteins showed that the meiotic recombination pathway is disrupted in mpa1. Chromosome pairing and early recombination appears normal, but progression to later stages of recombination and complete synapsis of homologous chromosomes are blocked.     

Desynapsis in Alocasia indica Schott

In a culture of Alocasia indica (2n=28), one plant was found to be desynaptic. At pachytene, pairing apparently was complete, but at diakinesis and metaphase I on the average only 2.36 and 1.53 bivalents respectively were found. Desynapsis is of the medium-strong type according to Prakken. Later meiotic stages were irregular and pollen sterility was 95%. The origin must have been spontaneous mutation.     

The influence of mutated genes on sporogenesis

Summary The course of meiosis in higher plants is controlled by a large number of genes, the function of which can be discerned by means of mutants showing any kind of meiotic anomaly. In general, there are three main groups of genes belonging to this system. The as-genes control the pairing behaviour of the homologous chromosomes, causing asynapsis in the mutated condition. The ds-genes are responsible for chiasma formation and chiasma frequency, causing desynapsis in the mutated condition. As- and ds-genes influence micro- and macrosporogenesis in a similar way but the ms-genes become effective only in microsporogenesis, resulting in a complete breakdown of meiosis at a stage specific for each gene of the group.In Pisum sativum, 58 mutants showing genetically conditioned meiotic anomalies have been cytogenetically analysed: 34 of them belong to the ds- and 7 to the as-group; one gene causes asynaptic as well as desynaptic effects; 13 genotypes are male sterile due to degeneration of the chromosomes; the remaining 3 genes cause less specific meiotic disturbances. The lethality of a mutant can be overcome by distinct environmental conditions but the mutant is sterile because of manifold meiotic anomalies.One gene in the Pisum genome controls the transition from the vegetative to the reproductive stage of the plants. Other genes influence the differentiation of the growing points in such a way that the sporogenic tissues are not formed. In these mutants, no sporocytes are present which can undergo meiosis.From the findings available for many species of the plant kingdom, it can be assumed that hundreds of genes controlling meiosis are present in the genome of each higher plant.The investigations were supported by the Ministry of Research and Technology of the Federal Republic of Germany and by the European Atomic Community.     

莱菌（Chlamydomonas reinhardtii)subcbn I基因的遗传学性质分析

通过将莱茵衣藻回复合成叶绿素ｂ能力的１４种回复突变株和野生型杂文并对其后代进行四分子分析与随机分析,发现导致回复突变的抑制基因ｓｕｂ位于第一染色体,并根据其连锁程度的不同初步鉴定出５个同功能的非等位ｓｕｂ基因。杂交分析表明ｓｕｂ基因不具有等位专一性,以及在促使ｃｂｎＩ基因重新获得合成叶绿素ｂ的能力的过程中具有单一基因决定性状的特点,不同的ｓｕｂ基因具有其独立的表型效应。ｓｕｂ／Ｓｕｂ杂合二倍体的表型分析证明ｓｕｂ基因是显性突变基因。多个非等位ｓｕｂ基因的存在及其上述特点,都显示出叶绿素ｂ的生物合成,可能存在多种途径或多种调控方式。     

The maize desynaptic1 mutation disrupts meiotic chromosome synapsis

In most eukaryotes, homologous chromosomes undergo synapsis during the first meiotic prophase. A consequence of mutations that interfere with the fidelity or completeness of synapsis can be failure in the formation or maintenance of bivalents, resulting in univalent formation at diakinesis and production of unbalanced spores or gametes. Such mutations, termed desynaptic mutations, can result in complete or partial sterility. We have examined the effect of the maize desynaptic1-9101 mutation on synapsis, using the nuclear spread technique and electron microscopy to examine microsporocytes ranging from early pachytene until the diplotene stage of prophase I. Throughout the pachytene stage, there was an average of about 10 sites of lateral element divergence (indicating nonhomologous synapsis), and during middle and late pachytene, an average of two and three sites of foldback (intrachromosomal) synapsis, per mutant nucleus, respectively. By the diplotene stage, the number of sites of lateral element divergence had decreased to seven, and there was an average of one foldback synapsis site per nucleus. Lateral element divergence and foldback synapsis were not found in spread pachytene nuclei from normal plants. These results imply that the normal expression of the dsy1 gene is essential for the restriction of chromosome synapsis to homologues. The abundance of nonhomologous synapsis and the persistence of extended stretches of unsynapsed axial elements throughout the pachytene stage of dsy1–9101 meiocytes suggests that this mutation disrupts both the fidelity of homology search and the forward course of the synaptic process. This mutation may identify a maize mismatch repair gene. Dev. Genet. 21:146–159, 1997. © 1997 Wiley-Liss, Inc.     

Mitochondrial DNA cytochrome b gene variation reveals different largemouth bass genealogies

A mitochondrial DNA character set based on cytochrome b gene variations is described that may be used in conjunction with established nuclear gene differences to assess largemouth bass Micropterus salmoides population structure and dynamics. Alignment of known cytochrome b sequences revealed two regions where the functional constraints of the molecule appear to be sufficiently reduced to allow several amino acid substitutions. Restriction analysis was used to probe nucleotide variation within one of these evolutionary hotspots, resulting in the discovery of fixed largemouth bass subspecific cytochrome b haplotypes. Application of two molecular character sets, one founded on fixed allelic variation in nuclear genes and the other on mtDNA cytochrome b diversity, revealed that in several Texas populations, where the Florida subspecies was introduced into extant populations of northern largemouth bass, hybridization was evident. The direction of the introgression vector could be determined through the combination of both character Sets.     

Genomic screening by 454 pyrosequencing identifies a new human IGHV gene and sixteen other new IGHV allelic variants

Complete and accurate knowledge of the genes and allelic variants of the human immunoglobulin gene loci is critical for studies of B cell repertoire development and somatic point mutation, but evidence from studies of VDJ rearrangements suggests that our knowledge of the available immunoglobulin gene repertoire is far from complete. The reported repertoire has changed little over the last 15 years. This is, in part, a consequence of the inefficiencies involved in searching for new members of large, multigenic gene families by cloning and sequencing. The advent of high-throughput sequencing provides a new avenue by which the germline repertoire can be explored. In this report, we describe pyrosequencing studies of the heavy chain IGHV1, IGHV3 and IGHV4 gene subgroups in ten Papua New Guineans. Thousands of 454 reads aligned with complete identity to 51 previously reported functional IGHV genes and allelic variants. A new gene, IGHV3-NL1*01, was identified, which differs from the nearest previously reported gene by 15 nucleotides. Sixteen new IGHV alleles were also identified, 15 of which varied from previously reported functional IGHV genes by between one and four nucleotides, while one sequence appears to be a functional variant of the pseudogene IGHV3-25. BLAST searches suggest that at least six of these new genes are carried within the relatively well-studied populations of North America, Europe or Asia. This study substantially expands the known immunoglobulin gene repertoire and demonstrates that genetic variation of immunoglobulin genes can now be efficiently explored in different human populations using high-throughput pyrosequencing.     

Isolation and characterization of valine-resistant mutants of Nicotiana plumbaginifolia

Summary Haploid mesophyll protoplasts of Nicotiana plumbaginifolia were mutagenized by UV-irradiation. Protoplast-derived colonies were then selected for valine resistance on a medium containing 5 or 10 mM valine. From the resistant calli, plants were regenerated. Resistance was inherited as a recessive Mendelian character in seven clones. Mutations conferring valine resistance were shown to be allelic. Protoplast-derived cells of L-valine-resistant plants were also resistant to L-threonine. Resistance to valine was based on a reduced valine uptake rate.