scholarly journals Domain Unknown Function DUF1668-Containing Genes in Multiple Lineages Are Responsible for F1 Pollen Sterility in Rice

2021 ◽  
Vol 11 ◽  
Author(s):  
Mitsukazu Sakata ◽  
Noriko Takano-Kai ◽  
Yuta Miyazaki ◽  
Hiroyuki Kanamori ◽  
Jianzhong Wu ◽  
...  

Postzygotic reproductive isolation maintains species integrity and uniformity and contributes to speciation by restricting the free gene flow between divergent species. In this study we identify causal genes of two Mendelian factors S22A and S22B on rice chromosome 2 inducing F1 pollen sterility in hybrids between Oryza sativa japonica-type cultivar Taichung 65 (T65) and a wild relative of rice species Oryza glumaepatula. The causal gene of S22B in T65 encodes a protein containing DUF1668 and gametophytically expressed in the anthers, designated S22B_j. The O. glumaepatula allele S22B-g, allelic to S22B_j, possesses three non-synonymous substitutions and a 2-bp deletion, leading to a frameshifted translation at the S22B C-terminal region. Transcription level of S22B-j and/or S22B_g did not solely determine the fertility of pollen grains by genotypes at S22B. Western blotting of S22B found that one major band with approximately 46 kDa appeared only at the mature stage and was reduced on semi-sterile heterozygotes at S22B, implying that the 46 kDa band may associated in hybrid sterility. In addition, causal genes of S22A in T65 were found to be S22A_j1 and S22A_j3 encoding DUF1668-containing protein. The allele of a wild rice species Oryza meridionalis Ng at S22B, designated S22B_m, is a loss-of-function allele probably due to large deletion of the gene lacking DUF1668 domain and evolved from the different lineage of O. glumaepatula. Phylogenetic analysis of DUF1668 suggested that many gene duplications occurred before the divergence of current crops in Poaceae, and loss-of-function mutations of DUF1668-containing genes represent the candidate causal genetic events contributing to hybrid incompatibilities. The duplicated DUF1668-domain gene may provide genetic potential to induce hybrid incompatibility by consequent mutations after divergence.

Genome ◽  
2006 ◽  
Vol 49 (10) ◽  
pp. 1209-1214 ◽  
Author(s):  
Marion S. Röder ◽  
Christian Kaiser ◽  
Winfriede Weschke

A number of mutations affecting seed development in barley (Hordeum vulgare L.) have been known for many years; however, to date, no research has been reported that elucidates the molecular structure of the causal genes. As a first step, we initiated the linkage mapping of the two shrunken endosperm genes seg8 and sex1 using microsatellite markers. The recessive gene seg8 was mapped in the centromeric region of chromosome 7H to a 4.6 cM interval flanked by markers GBM1516 and Bmag341. The recessive sex1 gene showed xenia effects and was located in the centromeric region of barley chromosome 6H, which is in accordance to the previously reported chromosomal location in the classical linkage map. It was flanked by markers GBM5012 and GBM1063 in a 4.2 cM interval. EST-derived microsatellite markers were used to establish the syntenic relationships to the genomic rice sequences. Two orthologous sites on rice chromosome 2 flanking a 4.1 Mb sequence had homology to the respective barley markers in the sex1 region. For the markers in the seg8 region orthologous sites on rice chromosome 6 were detected.


2014 ◽  
Vol 64 (4) ◽  
pp. 309-320 ◽  
Author(s):  
Mitsukazu Sakata ◽  
Yoshiyuki Yamagata ◽  
Kazuyuki Doi ◽  
Atsushi Yoshimura

The Nucleus ◽  
2021 ◽  
Author(s):  
Fajarudin Ahmad ◽  
Yuyu S. Poerba ◽  
Gert H. J. Kema ◽  
Hans de Jong

AbstractBreeding of banana is hampered by its genetic complexity, structural chromosome rearrangements and different ploidy levels. Various scientific disciplines, including cytogenetics, linkage mapping, and bioinformatics, are helpful tools in characterising cultivars and wild relatives used in crossing programs. Chromosome analysis still plays a pivotal role in studying hybrid sterility and structural and numerical variants. In this study, we describe the optimisation of the chromosome spreading protocol of pollen mother cells focusing on the effects of standard fixation methods, duration of the pectolytic enzyme treatment and advantages of fluorescence microscopy of DAPI stained cell spreads. We demonstrate the benefits of this protocol on meiotic features of five wild diploid Musa acuminata bananas and a diploid (AA) cultivar banana “Rejang”, with particular attention on pairing configurations and chromosome transmission that may be indicative for translocations and inversions. Pollen slides demonstrate regular-shaped spores except “Rejang”, which shows fertile pollen grains of different size and sterile pollen grains, suggesting partial sterility and unreduced gamete formation that likely resulted from restitutional meiotic divisions.


2005 ◽  
Vol 25 (8) ◽  
pp. 3076-3086 ◽  
Author(s):  
Flávio S. J. de Souza ◽  
Andrea M. Santangelo ◽  
Viviana Bumaschny ◽  
María Elena Avale ◽  
James L. Smart ◽  
...  

ABSTRACT The proopiomelanocortin (POMC) gene is expressed in the pituitary and arcuate neurons of the hypothalamus. POMC arcuate neurons play a central role in the control of energy homeostasis, and rare loss-of-function mutations in POMC cause obesity. Moreover, POMC is the prime candidate gene within a highly significant quantitative trait locus on chromosome 2 associated with obesity traits in several human populations. Here, we identify two phylogenetically conserved neuronal POMC enhancers designated nPE1 (600 bp) and nPE2 (150 bp) located approximately 10 to 12 kb upstream of mammalian POMC transcriptional units. We show that mouse or human genomic regions containing these enhancers are able to direct reporter gene expression to POMC hypothalamic neurons, but not the pituitary of transgenic mice. Conversely, deletion of nPE1 and nPE2 in the context of the entire transcriptional unit of POMC abolishes transgene expression in the hypothalamus without affecting pituitary expression. Our results indicate that the nPEs are necessary and sufficient for hypothalamic POMC expression and that POMC expression in the brain and pituitary is controlled by independent sets of enhancers. Our study advances the understanding of the molecular nature of hypothalamic POMC neurons and will be useful to determine whether polymorphisms in POMC regulatory regions play a role in the predisposition to obesity.


2014 ◽  
Vol 8 ◽  
pp. 120-126 ◽  
Author(s):  
Bal K. Joshi ◽  
Laxmi P. Subedi ◽  
Santa B. Gurung ◽  
Ram C. Sharma

Pollen analysis can be used to discriminate between different species, identify possible  interspecies hybrids, identify restorer and maintainer lines, useful to study genetics of  restorer gene, interaction between chromosome and cytoplasm and relationship between  parents. Pollen abortion system of male sterility is an important tool in hybrid rice  production and spikelet is the major yield components. Nine improved cultivars, six  landraces and three wild aborted cytoplasmic-genetic male sterile (CMS) lines were used to  analyze pollen and spikelet in F1 rice hybrids and their parents. The frequency of pollen  categories and its relationship to spikelet fertility were investigated. Pollen sterility of the  F1s was determined by staining pollen grains in 1% potassium iodide-iodine (I-KI) solution.  Spikelet fertility was determined by counting the total number of seed set in proportion to  the total number of spikelets. Correlation and regression coefficients for some traits were  computed. In hybrids, pollen fertility ranged from 0.5 to 82% and spikelet fertility from 0 to  87%. Pollen fertility varied from 28 to 97%, while spikelet fertility from 73 to 91% in pollen  parents. The highest and the lowest percentages of pollen fertility were found in Chaite-6  and Chiunde cultivars respectively. Spikelet fertility percentage varied widely among  hybrids and many hybrids had lower spikelet fertility percentage than their parents.  Therefore, it is of practical importance to understand the causes of high spikelet sterility in  hybrids for possible increase in spikelet fertility. Highly significant positive correlation was  found between stained round fertile (SRF) pollen and spikelet fertility. The positive value of  correlation and regression coefficient on SRF and spikelet fertility were found between F1  and mid parent, and F1 and male parent. High fertility of cross may be due to the presence of  a wide compatibility gene or restorer genes in the cultivar. Lower pollen and spikelet  fertility of the crosses was attributed to effect of the genetic background of the tester parent. Nepal Agric. Res. J. Vol. 8, 2007, pp. 120-126 DOI: http://dx.doi.org/10.3126/narj.v8i0.11605  


2016 ◽  
Vol 59 ◽  
pp. 29-37
Author(s):  
Olga Ivanchenko ◽  
Valentina Bessonova

This research was conducted to study pollen quality in woody plants in the city parks of Dnipro, which are located at various distances from the sources of anthropogenic pollution. It has been revealed that sterile pollen in its greatest abundance was present in plant species in the Park of Memory and Reconciliation and Molodyozhny park, as both are situated within the range of emission transfer from the Western Industrial Complex, while the least abundant sterile pollen was detected in the park named after Yu. Gagarin and that named after V. Dubinin. According to sterility indices, the pollen inBetula pendulaRoth. and that inAcer platanoidesL. were most sensitive to environmental pollution. In the city parks, the amounts of shrunk and abnormally shaped pollen grains increases; giant forms with grain diameters exceeding standard, as well as dwarf forms are not rare in occurrence. The highest percentage of pollen grains of atypical shape and size was observed in the same parks where the pollen sterility index had its highest values.


2012 ◽  
Author(s):  
◽  
Tiffany Langewisch

Maize S-type cytoplasmic male sterility (CMS-S) is a maternally inherited trait that prevents pollen grains from developing to maturity. CMS-S is associated with the high levels of a novel mitochondrial transcript, orf355/orf77. Cleavage of this RNA, mediated by the nuclear restorer Rf3, reverses the sterility. Rf3 was previously mapped on the long arm of chromosome 2. The goals of this research were to fine-map the locus and to identify Rf3 using a candidate gene approach. Genotyping of nearisogenic lines (NILs) mapped Rf3 to a 1.98 Mb region of 2L. Six candidate genes, all predicted to code for mitochondrially targeted pentatricopeptide repeat proteins (PPR), were PCR-amplified, sequenced, and compared from multiple Rf3-containing NILs and non-restoring rf3 inbreds. One PPR-Rf3 candidate gene had two consistent differences between multiple restoring and non-restoring lines. Gene expression in pre-emergent tassels from the fertility-restored and non-restored plants was compared. Within the 3 Mb region surrounding Rf3, 9 genes were differentially expressed between restoring and non-restoring lines, including genes that could code for an ATP-binding protein, an ATPase, and four PPR proteins. Although Rf3 has not yet been identified, this study has revealed five promising candidates.


2020 ◽  
Vol 33 (3-4) ◽  
pp. 205-219
Author(s):  
Lorenzo Ascari ◽  
Cristina Novara ◽  
Virginia Dusio ◽  
Ludovica Oddi ◽  
Consolata Siniscalco

AbstractHigh-quality pollen is a prerequisite for plant reproductive success. Pollen viability and sterility can be routinely assessed using common stains and manual microscope examination, but with low overall statistical power. Current automated methods are primarily directed towards the analysis of pollen sterility, and high throughput solutions for both pollen viability and sterility evaluation are needed that will be consistent with emerging biotechnological strategies for crop improvement. Our goal is to refine established labelling procedures for pollen, based on the combination of fluorescein (FDA) and propidium iodide (PI), and to develop automated solutions for accurately assessing pollen grain images and classifying them for quality. We used open-source software programs (CellProfiler, CellProfiler Analyst, Fiji and R) for analysis of images collected from 10 pollen taxa labelled using FDA/PI. After correcting for image background noise, pollen grain images were examined for quality employing thresholding and segmentation. Supervised and unsupervised classification of per-object features was employed for the identification of viable, dead and sterile pollen. The combination of FDA and PI dyes was able to differentiate between viable, dead and sterile pollen in all the analysed taxa. Automated image analysis and classification significantly increased the statistical power of the pollen viability assay, identifying more than 75,000 pollen grains with high accuracy (R2 = 0.99) when compared to classical manual counting. Overall, we provide a comprehensive set of methodologies as baseline for the automated assessment of pollen viability using fluorescence microscopy, which can be combined with manual and mechanized imaging systems in fundamental and applied research on plant biology. We also supply the complete set of pollen images (the FDA/PI pollen dataset) to the scientific community for future research.


2001 ◽  
Vol 11 (7) ◽  
pp. 1167-1174
Author(s):  
Klaus Mayer ◽  
George Murphy ◽  
Renato Tarchini ◽  
Rolf Wambutt ◽  
Guido Volckaert ◽  
...  

The nucleotide sequence was determined for a 340-kb segment of rice chromosome 2, revealing 56 putative protein-coding genes. This represents a density of one gene per 6.1 kb, which is higher than was reported for a previously sequenced segment of the rice genome. Sixteen of the putative genes were supported by matches to ESTs. The predicted products of 29 of the putative genes showed similarity to known proteins, and a further 17 genes showed similarity only to predicted or hypothetical proteins identified in genome sequence data. The region contains a few transposable elements: one retrotransposon, and one transposon. The segment of the rice genome studied had previously been identified as representing a part of rice chromosome 2 that may be homologous to a segment of Arabidopsis chromosome 4. We confirmed the conservation of gene content and order between the two genome segments. In addition, we identified a further four segments of the Arabidopsis genome that contain conserved gene content and order. In total, 22 of the 56 genes identified in the rice genome segment were represented in this set of Arabidopsis genome segments, with at least five genes present, in conserved order, in each segment. These data are consistent with the hypothesis that theArabidopsis genome has undergone multiple duplication events. Our results demonstrate that conservation of the genome microstructure can be identified even between monocot and dicot species. However, the frequent occurrence of duplication, and subsequent microstructure divergence, within plant genomes may necessitate the integration of subsets of genes present in multiple redundant segments to deduce evolutionary relationships and identify orthologous genes.


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