scholarly journals Intergeneric hybrids of Phalaenopsis 2166 x Vanda ‘Saint Valentine’ showing maternal inheritance: Genetic analysis based on ndhE partial gene

2020 ◽  
Vol 21 (11) ◽  
Author(s):  
Murni Dwiati ◽  
Agus Susanto ◽  
Lucky Prayoga

Abstract. Dwiati M, Susanto AH, Prayoga L. 2020. Intergeneric hybrids of Phalaenopsis 2166 x Vanda ‘Saint Valentine’ showing maternal inheritance: Genetic analysis based on ndhE partial gene. Biodiversitas 21: 5138-5145. Genetic characterization in the intergeneric hybridization of orchids employing a particular molecular marker, such as ndhE gene, is needed to avoid phenotypic plasticity. The hybridization between Phalaenopsis 2166 as a female parent and Vanda ‘Saint Valentine'as a male parent has been successfully made to produce various leaf shapes and colors of the hybrid seedlings, which tend to resemble those of the female parent. This study aims to assess whether the maternally phenotypic traits of the hybrids of Phalaenopsis 2166 x Vanda ‘Saint Valentine’ are congruent with the inheritance pattern of ndhE partial sequences. The result reveals that the ndhE partial sequences of the hybrids are seemingly similar to that of Phalaenopsis 2166 as the female parent rather than to that of Vanda ‘Saint Valentine’. It is also found that three hybrids, i.e. F1.9, F1.11, and F1.14 show slightly different ndhE partial sequences from those of the other hybrids in that some base substitutions are observed. In general, the ndhE partial sequences of the hybrids are maternally inherited. This finding provides a fact that maternally phenotypic traits of the hybrids of Phalaenopsis 2166 x Vanda ‘Saint Valentine’ have strong genetic background rather than environmental involvement.

2003 ◽  
Vol 128 (5) ◽  
pp. 724-730
Author(s):  
Thomas H. Boyle ◽  
Alexander Idnurm

Post-pollination barriers to intergeneric hybridization between Easter cactus [Hatiora gaertneri (Regel) Barthlott, H. rosea (Lagerheim) Barthlott, and H. ×graeseri Barthlott ex D. Hunt] and holiday cactus [Schlumbergera truncata (Haworth) Moran and S. ×buckleyi (Buckley) Tjaden] were determined and procedures were devised for circumventing these barriers. Examination of Hatiora and Schlumbergera pistils at 72 hours after intergeneric crosses indicated no abnormalities in pollen germination or pollen tube growth in the upper style. Pollen tubes of Hatiora were arrested in the lower half of Schlumbergera styles and failed to enter the ovary. Schlumbergera pollen tubes exhibited normal growth in Hatiora styles but most tubes lost directionality, burst, or failed to penetrate the micropyles after reaching the ovary. Three growth regulators (BA, GA3 and NAAm) were applied individually to ovaries of `Crimson Giant' Easter cactus after intergeneric crosses. GA3 and NAAm increased fruit set compared to the control (lanolin alone) or BA but none of the fruit harvested 160 days after pollination contained mature embryos. Four progeny were obtained when a short-styled S. ×buckleyi clone was crossed as a female parent with H. ×graeseri. Isozyme patterns and morphological characteristics confirmed that the four progeny were intergeneric hybrids. This is the first report of successful intergeneric hybridization between Hatiora and Schlumbergera. Chemical names used: N-(phenylmethyl)-1H-purine-6-amine [benzyladenine (BA)]; gibberellic acid (GA3); α-naphthaleneacetamide (NAAm).


Children ◽  
2021 ◽  
Vol 8 (2) ◽  
pp. 117
Author(s):  
Akiko Arakawa ◽  
Naotomo Kambe ◽  
Ryuta Nishikomori ◽  
Akiyo Tanabe ◽  
Masamichi Ueda ◽  
...  

We describe a patient who developed multiple granulomatous skin lesions after Bacille de Calmette et Guérin (BCG) vaccination without significant effect by topical corticosteroid, followed by painless cystic tumors on the bilateral knees and hands and inflammatory changes on ophthalmologic examination. A functional mutation in NOD2 was detected by a genetic analysis, and he was diagnosed as sporadic Blau syndrome. Since NOD2 acts as a sensor for the BCG component, it is possible that BCG vaccination may trigger granuloma formation in Blau syndrome patients with such genetic background.


2021 ◽  
Vol 7 (2) ◽  
pp. 205511692110254
Author(s):  
Ivona Orgonikova ◽  
Lorenzo Mari ◽  
Chiara Giannasi ◽  
Martí Pumarola i Batlle ◽  
Sebastien Behr ◽  
...  

Case summary In this report we describe the occurrence of intracranial meningioma in two adult cats from the same litter. The location of the meningioma varied: one tumour was at the level of the brainstem, and the other was affecting the temporal and piriform lobes. The cat with the brainstem meningioma was treated with radiotherapy and the littermate had a rostrotentorial craniectomy for tumour removal. Both cats had a histopathological diagnosis of grade I meningioma of a predominantly fibrous subtype. Relevance and novel information Cases of familial meningioma in cats have not previously been described in the veterinary literature. However, familial meningioma is well described in humans and it is possible that cases are underestimated in animals. We discuss the possible genetic background and other causes, as well as challenges we may face in veterinary medicine in identifying these associations.


Genetics ◽  
1996 ◽  
Vol 143 (1) ◽  
pp. 353-364 ◽  
Author(s):  
Jerry A Coyne

Abstract Females of Drosophila melanogaster and its sibling species D. simulans have very different cuticular hydrocarbons, with the former bearing predominantly 7,11-heptacosadiene and the latter 7-tricosene. This difference contributes to reproductive isolation between the species. Genetic analysis shows that this difference maps to only the third chromosome, with the other three chromosomes having no apparent effect. The D. simulans alleles on the left arm of chromosome 3 are largely recessive, allowing us to search for the relevant regions using D. melanogaster deficiencies. At least four nonoverlapping regions of this arm have large effects on the hydrocarbon profile, implying that several genes on this arm are responsible for the species difference. Because the right arm of chromosome 3 also affects the hydrocarbon profile, a minimum of five genes appear to be involved. The large effect of the third chromosome on hydrocarbons has also been reported in the hybridization between D. simulans and its closer relative D. sechellia, implying either an evolutionaly convergence or the retention in D. sechllia of an ancestral sexual dimorphism.


Author(s):  
Purabi Kaushik ◽  
Jnyanashree Saikia ◽  
Kabitabala Kalita ◽  
Rajjyoti Deka ◽  
J. Saharia

Background: Duck farming plays a significant role, next to chicken in the socio-economic uplift men of the rural farmers of North-East India. Pati duck is the most common duck breed in the Brahmaputra valley of Assam and the other common variety reared in North-East India is Chara-Chambeli, however it originatein Kerala. Genetic characterization plays a significant role for formulation of breeding strategies for improvement of any breed. Microsatellites are codominant in nature and are highly polymorphic. High level of allelic variation, co-dominant mode of inheritance and potential for automated analysis make them an excellent tool for genotyping, mapping and genetic characterization. Pati duck is the most common duck breed in the Brahmaputra valley of Assam and the other common variety reared in North-East India is Chara-Chambeli however its origin in Kerela. Therefore, the present investigation was carried out to characterize these two duck breeds using microsatellite markers to evaluate the genetic diversity in these two duck population. Methods: For the present study, Blood sample were collected from 50 Patiducks and 50 Chara-Chambeli ducks from different parts of North-East India. Assessment of genetic characterization of duck breeds of north-east region were carried out using 16 microsatellite markers and population genetics analysis were done by POPGENE software. Result: In the present study, all the studied loci were highly polymorphic. Analysis generated a total of 41 microsatellite alleles. The number of observed alleles (Na) with an overall mean of 1.93±0.258. However, the effective number of alleles (Ne) with a mean of 1.6933±0.2712. The Shannon’s information index was found to a mean value of 0.5685±0.1693. The overall means for observed (HO) and expected (He) heterozygosities were 0.2889±0.2477 and 0.5289±0.0853, respectively. The chi-square (χ2) test for Hardy-Weinberg equilibrium revealed that all the loci are in within Hardy-Weinberg equilibrium.


1988 ◽  
Vol 89 (1) ◽  
pp. 39-47 ◽  
Author(s):  
C. Gonzalez ◽  
J. Casal ◽  
P. Ripoll

Mutation in the gene merry-go-round (mgr) of Drosophila causes a variety of phenotypic traits in somatic and germinal tissues, such as polyploid cells, metaphasic arrest, postmeiotic cysts with 16 nuclei, and spermatids with four times the normal chromosome content. The most characteristic phenotype is the appearance of mitotic and meiotic figures where all chromosomes are arranged in a circle. Treatment with anti-mitotic drugs and the phenotype of double mutants mgr asp (asp being a mutation altering the spindle) show that these circular figures need a functional spindle for their formation. These abnormal figures are caused by monopolar spindles similar to those observed after different treatments in several organisms. All mutant traits indicate that mgr performs a function necessary for the correct behaviour of centrosomes, thus opening this organelle to genetic analysis.


Genetics ◽  
1982 ◽  
Vol 102 (2) ◽  
pp. 139-147
Author(s):  
Michael J Hynes

ABSTRACT A mutant producing very high levels of the acetamidase enzyme encoded by the amdS gene has been isolated in a strain containing the amdA7 mutation, which itself causes high levels of this enzyme. Genetic analysis has shown that this mutation, designated amdI66, is adjacent to the amdS gene and is cis-dominant in its effect. The amdI66 mutation has little effect on amdS expression when present in strains not containing the amdA7 mutation. Two other amdA mutations investigated also interact with the amdI66 mutation to result in high acetamidase levels. No interaction between amdI66 and any of the other putative regulatory genes affecting amdS expression has been observed. The amdI66 mutation has been located by fine structure mapping at the extreme end of the controlling region, which has previously been defined by genetic mapping (Hynes 1979). Analysis of this region has been extended by mapping new mutations resulting in loss of amdS expression. One of these defines the most extreme site capable of mutation to loss of gene function found so far.


1985 ◽  
Vol 63 (9) ◽  
pp. 1582-1585 ◽  
Author(s):  
Leslie G. Hickok

Abscisic acid normally inhibits growth and male sexual differentiation (antheridia formation) in gametophytes of the fern Ceratopteris. Abscisic acid resistant mutants show increased growth and sexual differentiation in comparison with the wild type when cultured in the presence of abscisic acid. Two different mutants that confer resistance to the effects of abscisic acid have been fully characterized. One shows moderate resistance and the other strong resistance. The mutations involve separate but linked loci. Recombination between the loci yields double mutant (cis) recombinants that exhibit additive effects and show exceptional levels of abscisic acid resistance.


Author(s):  
Hans Gerhard Steimer

Abstract Literary compositional drafts and working manuscripts preserve traces of the gradual process of writing and its different stages. In the static medium of print, genetic editions are confronted with the problem of depicting the dynamic evolution of texts. Presenting the variants in line-by-line synoptic display disregards the spatial arrangement on the manuscript pages. On the other hand, giving a topographic representation of the writing in diplomatic transcripts might stratify it into a few chronological layers but is unable to sufficiently reproduce the dynamic process to an elaborate degree. Consequently, the screen is better suited to visualise the writing process. The digital presentation of the ‘Homburg Folio’, the most important manuscript of Friedrich Hölderlin’s late work, offers not only the transcriptional record as known from print media but displays the process of writing and revision on each of the facsimile’s pages itself (https://homburgfolio.wlb-stuttgart.de). Thus, it is possible to visualise writing both as an act in time and its graphic result on the space of a page. It confines itself to the presentation of the genesis without any constitution of a text. The combination of these different operations has often led to errors. Decoupling the genetic analysis from the extrapolation of text reveals its potential.


Development ◽  
1998 ◽  
Vol 125 (7) ◽  
pp. 1217-1227 ◽  
Author(s):  
B.T. Kehl ◽  
K.O. Cho ◽  
K.W. Choi

The Drosophila notum, the dorsal body wall of the thorax, is subdivided genetically into longitudinal domains (Calleja, M., Moreno, E., Pelaz, S. and Morata, G. (1996) Science 274, 252–255). Two homeobox genes clustered in the iroquois complex, araucan and caupolican, regulate proneural genes and are required for development of sensory bristles in the lateral notum (Gomez-Skarmeta, J. L., del Corral, R. D., de la Calle-Mustienes, E., Ferres-Marco, D. and Modolell, J. (1996) Cell 85, 95–105). An iroquois-related homeobox gene, mirror, was recently isolated and is localized close to the iroquois complex region (McNeil, H., Yang, C.-H., Brodsky, M., Ungos, J. and Simon, M. A. (1997) Genes and Development 11, 1073–1082; this study). We show that mirror is required for the formation of the alula and a subset of sensory bristles in the lateral domain of the notum. Genetic analysis suggests that mirror and the other iroquois genes interact to form the alula as well as the sensory organs. Based on similarities between mirror and the iroquois genes in their genetic map positions, expression, protein structure and function, mirror is considered a new member of the iroquois complex and is involved in prepatterning sensory precursor cells in the lateral notum.


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