Genetische Untersuchung Sternbildender Bakterien

Summary Crossing experiments are performed with the starforming bacteriumPseudomonas echinoides, in order to ivestigate the genetical structure of the cells and the mechanism of the gen transfer. For this purpose mutants are produced mainly by nitrite. They are selectively marked by synthesis blocks and nonselectively by different pigment production. With these mutants reverse crosses and multioint testcrosses are performed. By quantitative evaluation of the crosses it is possible to arrange the sequence and the approximate distance of the gens to a linear chromosome map.All cells behave statistically equivalent during the genetical exchange. All mutants are sexual compatible. The experiments do not show any sexual polarity.

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Genetic diversity and its relationship to hybrid performance and heterosis in rice as revealed by PCR-based markers

Ten elite inbred lines (four japonica, six indica), chosen from those widely used in the hybrid rice breeding program at Human Hybrid Rice Research Center in China, were crossed to produce all possible hybrids excluding reciprocals. The 45 F₁ hybrids along with the ten parents were evaluated for eight traits of agronomic importance, including yield potential, in a replicated field trial. The ten parents were analyzed with 100 arbitrary decamer oligonucleotide primers and 22 microsatellite (simple sequence repeats, SSRs) primer sets via polymerase chain reaction (PCR). Out of the 100 random primers used, 74 were informative and amplified 202 non-redundant bands (variants) with a mean of 2.73 bands per polymorphic primer. All 22 microsatellite primer sets representing 23 loci in the rice genome showed polymorphisms among the ten parents and revealed 90 alleles with an average of 3.91 per SSR locus. Cluster analysis based on Nei's genetic distance calculated from the 291 (202 RAPDs, 89 SSRs) non-redundant variants separated the ten parental lines into two major groups that corresponds to indica and japonica subspecies, which is consistent with the pedigree information. Strong heterosis was observed in hybrids for most of the traits examined. For the 43 diallel crosses (excluding 2 crosses not heading), yield potential, its components (including panicles per plant, spikelets per panicle and 1000-grain weight) and their heterosis in F₁ hybrids showed a significant positive correlation with genetic distance. When separate analyses were performed for the three subsets, yield potential and its heterosis showed significant positive correlations with genetic distance for the 15 indica x indica crosses and the 6 japonica x japonica crosses; however, yield potential and its heterosis were not correlated with genetic distance for the 22 indica x japonica crosses. Results indicated that genetic distance measures based on RAPDs and SSRs may be useful for predicting yield potential and heterosis of intra-subspecific hybrids, but not inter-subspecies hybrids.     

Genetics of Heading Time in Wheat (TRITICUM AESTIVUM L.). II. the Inheritance of Vernalization Response

The inheritance of vernalization response was studied in crosses involving four spring wheats (Sonora 64 (S), Pitic 62 (P), Justin (J) and Thatcher (T)) and three winter wheats (Blackhull (B), Early Blackhull (E) and Extra Early Blackhull (EE)).—All winter cultivars were highly responsive to vernalization, and Pitic 62 was the only spring cultivar whose time to heading was significantly accelerated following cold treatments. When vernalized and grown under long days, spring and winter cultivars became comparable in their heading response, indicating that cold requirement is the major attribute differentiating the heading behavior of true spring and true winter wheats.—Inheritance of growth habit in the F₁ generation of a five-parent diallel cross showed dominance of the spring character in all spring x winter crosses. Depending on the cross, one or two duplicate major genes governing growth habit were detected in F₂, F₃ and backcross generations grown in the field under long days in the absence of vernalizing temperatures. In some spring x winter crosses most of the variation in heading time among spring segregates could be attributed to the effects of major genes conditioning growth habit. In other crosses the heading patterns appeared more complex, indicating that genes with smaller effects are also involved in the control of heading response under spring or summer environments.—Evidence was presented supporting the hypothesis that the cultivar Pitic 62 carries a different allele at one of the two major loci governing its spring habit. This allele was associated with some response to vernalization and acted as a dominant gene determining earliness under low temperature vernalization, but as a partially recessive gene determining lateness in the absence of vernalizing temperatures. Genotypes were assigned to five cultivars as follows: S, CC DD; P, CC D'D'; J, cc DD; B and EE, cc dd.—The presence of major and minor genes and of multiple alleles governing response to photoperiod and vernalization was discussed in relation to the genetic manipulation of the heading response and to breeding wheat cultivars with specific or broad adaptation.     

Uncovering of major genetic factors generating naturally occurring variation in heading date among Asian rice cultivars

To dissect the genetic factors controlling naturally occurring variation of heading date in Asian rice cultivars, we performed QTL analyses using F₂ populations derived from crosses between a japonica cultivar, Koshihikari, and each of 12 cultivars originating from various regions in Asia. These 12 diverse cultivars varied in heading date under natural field conditions in Tsukuba, Japan. Transgressive segregation was observed in 10 F₂ combinations. QTL analyses using multiple crosses revealed a comprehensive series of loci involved in natural variation in flowering time. One to four QTLs were detected in each cross combination, and some QTLs were shared among combinations. The chromosomal locations of these QTLs corresponded well with those detected in other studies. The allelic effects of the QTLs varied among the cross combinations. Sequence analysis of several previously cloned genes controlling heading date, including Hd1, Hd3a, Hd6, RFT1, and Ghd7, identified several functional polymorphisms, indicating that allelic variation at these loci probably contributes to variation in heading date. Taken together, the QTL and sequencing results indicate that a large portion of the phenotypic variation in heading date in Asian rice cultivars could be generated by combinations of different alleles (possibly both loss- and gain-of-function) of the QTLs detected in this study.     

Mapping of QTLs conferring extremely early heading in rice (Oryza sativa L.)

Two genes related to extremely early heading were identified in populations derived from crosses between Hoshinoyume, a variety adapted to the northernmost limit of rice cultivation (Hokkaido), and Nipponbare, a variety adapted to the temperate region of Japan. The segregations for heading date clearly revealed that a two-gene model determined the extremely early heading in the F₂ and BC₁F₁ populations under natural field conditions in Hokkaido. Using molecular markers corresponding to ten known quantitative trait loci (QTLs) for heading date, we carried out QTL analysis in the BC₁F₁ population and detected two QTLs, qDTH-7-1 and qDTH-7-2, both on chromosome 7, and observed epistatic interaction between them. We conclude that the recessive alleles of these two genes contribute to extremely early heading for the adaptation to Hokkaido environment and to stable rice production in Hokkaido. The relationships between the two QTLs identified in this study and known QTLs are discussed.     

Genetic mapping and biochemical characterization of mutations in the mannonic hydrolyase structural gene of Escherichia coli K 12

Summary Mutants of E. coli specifically deficient for the enzyme mannonic hydrolyase have been isolated. These strains are unable to metabolize glucuronate but still normally grow on galacturonate; inducibility for the other glucuronate-induced enzymes is not modified.The position of these mutations called uxuA locus in relation to the pyrB-guaC region, and probably near 85.5 minutes, was established by sexual crosses and by P₁ transductionBiochemical characterization of uxuA mutants using thermosensible mutants was achieved by means of thermal inactivation and kinetic studies. Experimental results strongly suggest that uxuA locus is the structural gene of the mannonic hydrolyase.

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Ce mémoire sera inclus dans les travaux présentés par Janine Robert-Baudouy pour l'obtention du grade de «Docteur ès Sciences Physiques» (Université Claude Bernard de Lyon).

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Mémoire présenté par F. Gros     

Genetische Mosaike in der M 2 bei Oenothera hookeri nach Behandlung mit Meterwellen

Zusammenfassung In der M₂ nach mutagener Behandlung von Pollen und Pflanzen von Oenothera hookeri traten morphologische Chimären auf, die sich als genetische Mosaike erwiesen. Es handelt sich um Abweichungen von Blattform und Blattfarbe. Die abweichenden Sektoren der Pflanzen erwiesen sich durch die Spaltung in der Nachkommenschaft als heterozygot für eine Mutation. Die Mutanten werden beschrieben. Die Mosaikpflanzen lassen Rückschlüsse zu auf die Wachsturnsordnung im Vegetationskegel und bei der Blattbildung. Das verspätete Auftreten der Mutationen wird interpretiert als eine durch die mutagene Behandlung ausgelöste genetische Labilität, die in der M₃ abgeklungen ist.

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Genetic mosaics in the second generation of Oenothera hookeri after treatment with radiowaves

Summary Morphological mosaic plants were observed in the second generation after a mutagenic treatment of pollen and plants of Oenothera hookeri. The abnormal parts showed differences in colour or form of the leaves. The progeny of the normal parts were normal, the abnormal sectors gave rise to several mutants. This proved the plants to be genetic mosaics. The mutants are described. The mosaics lead to conclusions about the growth in the apex and the leaf primordium. The delay in the occurrence of the mutations is interpreted as a genetic lability after the mutagenic treatment.

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Angenommen durch W. Seyffert     

Genetic mapping and biochemical characterization of mutations affecting altronic hydrolyase structural gene in Escherichia coli K 12

Summary Mutants of E. coli specifically deficient for the enzyme altronic hydrolyase have been isolated. These strains are unable to metabolize galacturonate but still normally grow on glucuronate; inducibility for the other galacturonate-induced enzymes is not modified.The position of these mutations called uxaA locus in relation to the argG, tolC and metC markers was established both by sexual crosses and by P₁ transduction; evidence is presented that uxaA is located between argG and tolC.Biochemical characterization of uxaA mutants using thermosensible revertants or mutants was achieved by means of thermal inactivation and kinetic parameters determination. Experimental results strongly suggest that uxaA locus is the structural gene of the altronic hydrolyase enzyme.

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Ce mémoire sera inclus dans les travaux présentés par Raymond Portalier pour l'obtention du grade de «Docteur ès Sciences» (Université Claude Bernard de Lyon).

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Mémoire présenté par F. Gros     

Zur Natur Der Ausgedehnten Mutationen Des Coliphagen T4

Summary No recombination could be observedwithin three extended mutations (block mutations) of the rII region of phage T4. The block mutations are studied under two different conditions, where (1) both parental particles contained an identical block mutation, and where (2) a block mutation was present in only one parent, while the other contained a point mutation, or was wild type at the corresponding location.In further experiments it was shown that the presence of a block mutation in only one parent reduces recombinationoutside the block. This interference decreases with increasing distance between the block mutation and the other sides.Although up to now no difference in density could be observed between wild type particles and block mutants, the genetic data which are reported here do support the interpretation that block mutations represent deletions within the genetic material.

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Dissertation an der Mathematisch-Naturwissenschaftlichen Fakultät der Universität zu Köln, eingereicht im Januar 1962.     

Effect of the mouse scid mutation on meiotic recombination

The goal of this study was to determine the effect of the mouse severe combined immunodeficiency (scid) mutation on the rate of meiotic recombination, by standard backcross linkage analysis. For this purpose, we examined four crosses that involved F₁ hybrid animals heterozygous for the strain C57BL/6 and BALB/c genomes. In one set of reciprocal crosses, F₁ animals were homozygous scid/scid, and in a second set of reciprocal crosses, F₁ mice were homozygous wild-type (+/+) at the scid locus. Backcross progeny were typed for recombination between selected genetic markers on mouse Chromosomes (Chrs) 1, 4, 6, 7, 9, 15, and 17. Although some differences in recombination were observed over some intervals, the expression of the SCID phenotype did not appear to have a major or consistent effect on meiotic recombination. Received: 4 October 1995 / Accepted: 2 April 1996     

Biochemical composition of maize (Zea mays L.) pollen

Summary Mean percentages of sugars, water-soluble polysaccharides, starch, total carbohydrates and lipids were 40.1, 7.4, 28.6, 76.1, and 1.8 respectively. Differences among the mutants were found only for water-soluble polysaccharides with both wx and sh ₂ decreasing the percentage a small but significant amount. In terms of the various carbohydrates measured, no correlation was found between the expression of these mutants in the pollen and the kernel.

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Zusammenfassung Die Untersuchung des Kohlenhydrat- und Lipid-Gehaltes im Pollen der Endosperm-Mutanten waxy, shrunken und sugary vom Mais ergab einen gemittelten Gehalt an Zucker von 40,1%, wasserlöslichen Polysacchariden 7,4%, Stärke 28,6, Gesamtkohlenhydraten 76,1% und Lipiden 1,8%.Unterschiede zwischen den Mutanten wurden lediglich hinsichtlich der wasserlöslichen Polysaccharide gefunden, und zwar bei wx und sh ₂, die einen signifikant niedrigeren Gehalt aufwiesen.Hinsichtlich der verschiedenen analysierten Kohlenhydrate wurde keine Korrelation zwischen der Expression der Mutanten im Pollen und in den Karyopsen gefunden.

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Herrn Professor Dr. J. Straub (Köln-Vogelsang) zu seinem 60. Geburtstag gewidmet.

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Journal Series Paper No. 3621, Florida Agricultural Experiment Station.     

Further studies on colchicine-resistant mutants of Chlamydomonas reinhardi

Five previously isolated colchicine-resistant mutants are shown to be cross-resistant to vinblastine. Inclusion of vinblastine in the medium actually improves the growth of four of the mutants and inclusion of colchicine in the medium improves the growth of all of them. ¹⁴C-colchicine uptake into the mutants is similar to wild type. Genetic crosses indicate that there are at least two loci for colchicine resistance although very poor zygote germination in some crosses with these mutants has hindered extensive genetic analysis.     

Prediction of progeny variation in oat from parental genetic relationships

Summary The ability to predict agronomic performance of progeny from a cross would be a great benefit to plant breeders in selecting parents. The predictive value of parental genetic relationships estimating F₁ progeny means and F₄ family variances of nine argronomic traits was tested in 76 oat crosses, using genetic distance measures based on coefficients-of-parentage, quantitatively inherited morphological characters, and discretely inherited biochemical and morphological characters. Coefficients-of-parentage were better predictors of F₁ performance than similarity measures derived from plant morphology or discretely inherited characters. Combined distance measures were better estimators of F₁ specific combining ability (SCA) effects than any single measure. Among cultivars of similar adaptation and quantitative morphology, crosses between parents with high coefficients-of-parentage gave higher SCA effect values than crosses of distantly related parents for grain yield and total biomass. The opposite was found for crosses among cultivars of different adaptation or quantitative morphology. The best predictor of trait variances among F₄ families was coefficients-of-parentage. Crosses between more distantly related parents produced larger variances among families than crosses between closely related parents for plant biomass. For grain yield, test weight, heading date, grain filling period, and maturity date, crosses between more closely related parents produced larger among-family variances than crosses of distantly related parents. Crosses between more distantly related parents involved at least one parent unadapted to central New York, and resulted in most of the progeny being generally unadapted. This, in part, may account for the low genetic variances for heading date, test weight, and grain yield in crosses of distantly related parents.     

Isolation of a major genetic interaction associated with an extreme phenotype using assorted F2 populations in rice

Detection of quantitative trait loci (QTLs) is dependent on the materials used in the analysis, as different combinations of parental materials may lead to different outcomes in QTLs for the same trait. On the other hand, an extreme phenotype associated with a given trait implies the potential involvement of a particular allele in various allelic interactions. A genetic factor associated with such an extreme phenotype may frequently be identified from various genetic populations consisting of different parental combinations. In this study, we attempted to uncover the genetic factor associated with extremely early heading date in rice, using various F2 populations. Heading date in rice has been characterized by at least 19 QTLs, from which 12 genes have been identified. A58, a rice strain with an extremely early heading date, is adapted to Hokkaido, the northernmost limit of rice cultivation. Six F2 populations derived from crosses of A58 with six other strains displayed a range of heading dates. Genotyping using 19 QTL markers indicated that the A58 allele of the Ghd7 locus was present in most F2 individuals exhibiting extremely early heading dates. This analysis also demonstrated that when the wild-type Ehd1 allele was present, the Ghd7 allele from A58 accelerated floral induction. The results of this study demonstrate that assorted F2 populations are valuable materials for comprehensive genotyping to explore major genetic factors for extreme phenotypes, and that this methodology is broadly applicable to other unknown traits.     

Genetic alleviation of the self-fertilization complication when hybridizing monoecious Gelidium vagum

Fundamental genetic studies were initiated for the monoecious red alga Gelidium vagum. Color and sterility mutants were isolated and characterized to provide genetic tools, initially to identify hybrid plants when they occurred in crosses, and secondarily to eliminate self-fertilization altogether. When fertility phenotypes were scored, rapid onset of reproduction in culture was favored by long day-length, moderately high irradiance levels from fluorescent lights, warm temperature and the addition of Tris buffer to the medium. A recessive green mutant (designated grn 1) was characterized and used in subsequent crosses to allow a clear distinction between non-hybrid (green) and hybrid (red) offspring. Additional color mutants and a variety of reproductive mutants were also isolated and characterized. Male-sterile mutants had phenotypes ranging from apparently normal plants to those that produced no spermatia. Female-sterile mutants also included a variety of phenotypes, some plants having post-fertilization malfunctions during the development of the carposporophyte. Only a fraction of the sterility mutations have been phenotypically or genetically characterized, but some are straightforwardly inherited as stable, nuclear, single-gene defects. From the genetic recombination pattern, one female-sterile mutant may be loosely linked (39 cMorgans) to the grn 1 marker gene. Male sterility very effectively eliminated selfing without affecting the production of carpospores in crosses, thereby overcoming one of the most serious genetic difficulties in working with this monoecious species.     

Fine Mapping of <Emphasis Type="Italic">qHD4-1</Emphasis>, a QTL Controlling the Heading Date,to a 20.7-kb DNA Fragment in Rice (<Emphasis Type="Italic">Oryza sativa</Emphasis> L.)

A library consisting of 1,123 single-segment substitution lines (SSSLs) in the same genetic background of an elite rice variety Huajingxian74 (HJX74) was evaluated for heading date. From this library, the SSSL W05-1-11-5-16-2-5 with the substituted interval of PSM103—RM348-OSR15-PSM382-RM131-RM127—RM280 was found having a gene, which stably performed extreme late heading date which performed stable and late heading in the different environments of Shandong, Guangdong, and Hainan. To map the gene governing heading date, the SSSL W05-1-11-5-16-2-5 was crossed with the recipient HJX74 to develop an F₂ segregating population. The distribution of late and early heading plants in this population fitted a segregation ratio of 3:1, indicating the late heading was controlled by a dominant gene. The gene locus for heading date was tentatively designated as qHD4-1. Using a random sample of 460 individuals from the F₂ segregation population, the qHD4-1 locus was mapped between two SSR markers RM3335 and RM17572, with genetic distances of 0.1 and 0.2 cM, respectively. For fine mapping of qHD4-1, a large F_2:3 segregating population of 3,000 individuals were developed from F₂ plants heterozygous in the RM3335-RM17572 region. Recombinants analyses further mapped qHD4-1 to an interval of 20.7-kb-bounded WB05 and the WB06. Sequence analysis of this 20.7-kb region revealed that it contains three open reading frames (ORFs), encoding wall-associated receptor kinase-like 5, putative F-box domain containing protein, and putative arogenate/prephenate dehydratase. Of them, ORF1, predicting to encode serine/threonine kinase, is considered the most likely as the candidate gene. The genetic and physical map of the qHD4-1 locus will be very useful in molecular cloning of the qHD4-1gene.     

Biogenesis of mitochondria 27

Summary The isolation and characterization of five new mutants affecting mitochondrial protein synthesis in S. cerevisiae is reported. Each mutation confers in vivo resistance to the macrolide antibiotic spiramycin which acts by inhibiting mitochondrial protein synthesis in sensitive yeast. The mutants are distinguishable on the basis of their in vivo cross resistance to other antibiotics, their biochemical properties and genetic behaviour. Genetic analysis indicates the mode of inheritance to be nuclear for one mutation and cytoplasmic for the other four. Recombination analysis performed on crosses between different cytoplasmic determinants, together with data from monofactorial crosses of each determinant with sensitive strains, demonstrates at least two and possibly three cytoplasmic genetic loci conferring spiramycin resistance.The protein synthesizing activities of mitochondria isolated from the mutant strains range in response to spiramycin and other antibiotics from strong resistance through partial resistance to complete sensitivity. Based on this data the mutants showing strong antibiotic resistance in vitro might be simply classified as mitochondrial ribosome mutants and mutants sensitive in vitro as mitochondrial membrane mutants; however mutants showing partial resistances are not so readily accommodated in either class. The diverse biochemical properties cannot be correlated with the different genetic loci described; indeed three mutations, each resulting in different biochemical behaviour appear to occur at the same locus. The results are interpreted as providing further evidence for an earlier proposal of mitochondrial membrane-ribosome interactions.     

Crossing analysis of sorbose resistant mutants of Neurospora crassa

Summary After treatment of the conidia of Neurospora crassa with nitrous acid 19 of the resulting mutants were selected for their resistance to sorbose, an agent which has a toxic effect on the wild type. The selected sorbose resistant mutants were analyzed genetically by crossing them with tester strains containing known markers. Mutational sites were thus found to be located on at least 5 of the full complement of 7 linkage groups. 9 sites were found to be located on the left arm of linkage group VI near the ylo-marker. These were so far not separable by recombinational analysis and therefore seem to represent a single gene-locus (A). Other sorbose resistant sites were mapped on linkage groups I, III (gene C), V and VII (gene B). Another site which has not yet been definitely located is not closely linked to any of the aforementioned. One site each on linkage groups I and VI were mapped more precisely by means of 3-point crosses. These crosses permitted the location of these sites of sorbose resistance in regard to neighbouring markers. From these crosses it is concluded that the mutation of any 1 of at least 6 different chromosomal genes can cause the formation of a sorbose resistant phenotype. The mutation of any 1 of 4 of these genes could result in a mutant with an altered sorbose permease system or containing a suppressor which decreases the efficiency of the permease system.

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I. Teil einer Habilitationsschrift bei der Naturwissenschaftlichen Fakultät der Universität München.     

Vergleichende Untersuchungen an HNO2-Inaktivierten und UV-Inaktivierten Bakteriophagen T4

Summary The inactivation of phage T4 by nitrous acid (HNO₂) is essentially an exponential function of time of treatment. HNO₂-inactivated T4 is able to undergo multiplicity reactivation, and genetic markers may be rescued by live phage, however, the extent of both effects is appreciably less than after UV-inactivation. Also, the survival of phenotypic function of the cistronsr II-A andr II-B is lower with HNO₂-treatment than with a UV-irradiation of a corresponding number of hits.The reduced effects are quantitatively accounted for by the assumption of lethal hits blocking early steps of infection. These early-step damages amount to approximately 1/6 of the total hit number; it is still unknown whether they occur in DNA or in protein. Some indication for the occurrence in protein comes from the result that the host-killing efficiency of HNO₂-inactivated phage is reduced at a similar rate as these early-step damages occur. However, at least 5/6 of the lethal hits are due to chemical changes within the DNA, as can be calculated from the results of multiplicity reactivation, marker rescue, and phenotypic survival of therII-cistrons.

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