scholarly journals High Temperature-induced Spindle Destabilization Results in Aborted Pollen Production in Populus

2021 ◽  
Author(s):  
Zhiqun Li ◽  
Yifan Zhao ◽  
Xuetong Cheng ◽  
Bo Kong ◽  
Yaru Sang ◽  
...  
Keyword(s):  
High Temperature ◽  
Chromosome Segregation ◽  
2N Gametes ◽  
Male Flower ◽  
Pollen Grains ◽  
Pollen Abortion ◽  
Duration Of Treatment ◽  
Male Gametes ◽  
Microtubular Cytoskeleton ◽  
Spindle Microtubules

Abstract High temperature can induce the production of 2n gametes and aborted pollen during microsporogenesis in Populus canescens. However, the mechanism by which high temperature induces pollen abortion remains unknown. Here, pollen abortion was induced by exposing male flower buds of P. canescens to 38 and 41 °C; pollen morphology, meiotic abnormalities, defects of the meiotic microtubular cytoskeleton, and tapetum development were characterized, and expression analysis of the Actin gene was conducted. We found that the dominant meiotic stage, temperature, and duration of treatment significantly affected the percentage of high temperature-induced aborted pollen. Damaged spindle microtubules and depolymerized microtubular cytoskeletons were observed, which resulted in many lagging chromosomes at anaphase Ⅰ and Ⅱ, as well as aneuploid male gametes and micronuclei, generating aborted pollen grains. Tapetum disintegration was also delayed. However, the anther dehisced normally, and some viable pollen grains were released, suggesting that the delayed degradation of the tapetum was not responsible for pollen abortion. A significant reduction in PtActin gene expression was detected in treated cells, indicating that spindle actin was disrupted. The spindle actin appeared to protect cells against chromosome segregation errors during meiosis.

Inheritance and microsporogenesis of a synaptic mutant (sy-2) from Solanum commersonii Dun.

1986 ◽  
Vol 28 (4) ◽  
pp. 520-524 ◽  
Author(s):  
S. A. Johnston ◽  
R. W. Ruhde ◽  
M. K. Ehlenfeldt ◽  
R. E. Hanneman Jr.
Keyword(s):  
Chromosome Segregation ◽  
2N Gametes ◽  
Pollen Grains ◽  
Pollen Sterility ◽  
Crossing Over ◽  
2N Pollen ◽  
Solanum Commersonii ◽  
Stainable Pollen ◽  
Tetrad Stage ◽  
Meiotic Mutants

A mutant has been found in diploid Solanum commersonii (2n = 2x = 24) in which no bivalents are formed during microsporogenesis. This trait, a simply inherited recessive, has been designated sy-2. It conditions high levels of pollen sterility through random chromosome segregation at anaphase I. Only the nucleolar-associated chromosomes appear to segregate non-randomly, possibly due to the fusion of the nucleoli as cells near diakinesis. Branched spindle configurations result in multipolar telophase I arrangements, yielding from one to seven pollen grains at the tetrad stage. Most of the stainable pollen produced appears to be 2n. The 2n pollen formed by this mechanism should bear the exact genotype of the parent, since no crossing-over occurs.Key words: Solanum, potato, 2n gametes, mutants (meiotic), mutants (synaptic).

scholarly journals Differential requirement for Bub1 and Bub3 in regulation of meiotic versus mitotic chromosome segregation

2020 ◽  
Vol 219 (4) ◽  
Author(s):  
Gisela Cairo ◽  
Anne M. MacKenzie ◽  
Soni Lacefield
Keyword(s):  
Chromosome Segregation ◽  
Protein Phosphatase ◽  
Mitotic Chromosome ◽  
Budding Yeast ◽  
Meiotic Chromosome ◽  
Protein Phosphatase 1 ◽  
Aurora B ◽  
Chromosome Missegregation ◽  
Anaphase Onset ◽  
Spindle Microtubules

Accurate chromosome segregation depends on the proper attachment of kinetochores to spindle microtubules before anaphase onset. The Ipl1/Aurora B kinase corrects improper attachments by phosphorylating kinetochore components and so releasing aberrant kinetochore–microtubule interactions. The localization of Ipl1 to kinetochores in budding yeast depends upon multiple pathways, including the Bub1–Bub3 pathway. We show here that in meiosis, Bub3 is crucial for correction of attachment errors. Depletion of Bub3 results in reduced levels of kinetochore-localized Ipl1 and concomitant massive chromosome missegregation caused by incorrect chromosome–spindle attachments. Depletion of Bub3 also results in shorter metaphase I and metaphase II due to premature localization of protein phosphatase 1 (PP1) to kinetochores, which antagonizes Ipl1-mediated phosphorylation. We propose a new role for the Bub1–Bub3 pathway in maintaining the balance between kinetochore localization of Ipl1 and PP1, a balance that is essential for accurate meiotic chromosome segregation and timely anaphase onset.

Abscisic acid prevents pollen abortion under high-temperature stress by mediating sugar metabolism in rice spikelets

2018 ◽  
Vol 165 (3) ◽  
pp. 644-663 ◽  
Author(s):  
Islam Md. Rezaul ◽  
Feng Baohua ◽  
Chen Tingting ◽  
Fu Weimeng ◽  
Zhang Caixia ◽  
...  
Keyword(s):  
Abscisic Acid ◽  
High Temperature ◽  
Temperature Stress ◽  
Sugar Metabolism ◽  
High Temperature Stress ◽  
Pollen Abortion

scholarly journals Functional Analysis of Kinetochore Assembly in Caenorhabditis elegans

2001 ◽  
Vol 153 (6) ◽  
pp. 1209-1226 ◽  
Author(s):  
Karen Oegema ◽  
Arshad Desai ◽  
Sonja Rybina ◽  
Matthew Kirkham ◽  
Anthony A. Hyman
Keyword(s):  
Caenorhabditis Elegans ◽  
Chromosome Segregation ◽  
Mitotic Chromosome ◽  
Mitotic Chromosomes ◽  
Cell Stage ◽  
Kinetochore Assembly ◽  
Chromosomal Passenger ◽  
Complete Failure ◽  
Spindle Microtubules ◽  
The One

In all eukaryotes, segregation of mitotic chromosomes requires their interaction with spindle microtubules. To dissect this interaction, we use live and fixed assays in the one-cell stage Caenorhabditis elegans embryo. We compare the consequences of depleting homologues of the centromeric histone CENP-A, the kinetochore structural component CENP-C, and the chromosomal passenger protein INCENP. Depletion of either CeCENP-A or CeCENP-C results in an identical “kinetochore null” phenotype, characterized by complete failure of mitotic chromosome segregation as well as failure to recruit other kinetochore components and to assemble a mechanically stable spindle. The similarity of their depletion phenotypes, combined with a requirement for CeCENP-A to localize CeCENP-C but not vice versa, suggest that a key step in kinetochore assembly is the recruitment of CENP-C by CENP-A–containing chromatin. Parallel analysis of CeINCENP-depleted embryos revealed mitotic chromosome segregation defects different from those observed in the absence of CeCENP-A/C. Defects are observed before and during anaphase, but the chromatin separates into two equivalently sized masses. Mechanically stable spindles assemble that show defects later in anaphase and telophase. Furthermore, kinetochore assembly and the recruitment of CeINCENP to chromosomes are independent. These results suggest distinct roles for the kinetochore and the chromosomal passengers in mitotic chromosome segregation.

scholarly journals Melatonin Alleviates High Temperature-Induced Pollen Abortion in Solanum lycopersicum

Molecules ◽  
2018 ◽  
Vol 23 (2) ◽  
pp. 386 ◽  
Author(s):  
Zhen-Yu Qi ◽  
Kai-Xin Wang ◽  
Meng-Yu Yan ◽  
Mukesh Kanwar ◽  
Dao-Yi Li ◽  
...  
Keyword(s):  
High Temperature ◽  
Solanum Lycopersicum ◽  
Pollen Abortion

scholarly journals Insights from the reconstitution of the divergent outer kinetochore of Drosophila melanogaster

Open Biology ◽  
2016 ◽  
Vol 6 (2) ◽  
pp. 150236 ◽  
Author(s):  
Yahui Liu ◽  
Arsen Petrovic ◽  
Pascaline Rombaut ◽  
Shyamal Mosalaganti ◽  
Jenny Keller ◽  
...  
Keyword(s):  
Drosophila Melanogaster ◽  
Chromosome Segregation ◽  
Functional Organization ◽  
Histone H3 Variant ◽  
Centromeric Protein ◽  
Spindle Microtubules ◽  
Specialized Region ◽  
Structural Methods ◽  
Mitosis And Meiosis ◽  
Shed Light

Accurate chromosome segregation during mitosis and meiosis is crucial for cellular and organismal viability. Kinetochores connect chromosomes with spindle microtubules and are essential for chromosome segregation. These large protein scaffolds emerge from the centromere, a specialized region of the chromosome enriched with the histone H3 variant CENP-A. In most eukaryotes, the kinetochore core consists of the centromere-proximal constitutive centromere-associated network (CCAN), which binds CENP-A and contains 16 subunits, and of the centromere-distal Knl1 complex, Mis12 complex, Ndc80 complex (KMN) network, which binds microtubules and contains 10 subunits. In the fruitfly, Drosophila melanogaster, the kinetochore underwent remarkable simplifications. All CCAN subunits, with the exception of centromeric protein C (CENP-C), and two KMN subunits, Dsn1 and Zwint, cannot be identified in this organism. In addition, two paralogues of the KMN subunit Nnf1 (Nnf1a and Nnf1b) are present. Finally, the Spc105R subunit, homologous to human Knl1/CASC5, underwent considerable sequence changes in comparison with other organisms. We combined biochemical reconstitution with biophysical and structural methods to investigate how these changes reflect on the organization of the Drosophila KMN network. We demonstrate that the Nnf1a and Nnf1b paralogues are subunits of distinct complexes, both of which interact directly with Spc105R and with CENP-C, for the latter of which we identify a binding site on the Mis12 subunit. Our studies shed light on the structural and functional organization of a highly divergent kinetochore particle.

scholarly journals Effect of high temperature on the reproductive development of chickpea genotypes under controlled environments

2012 ◽  
Vol 39 (12) ◽  
pp. 1009 ◽  
Author(s):  
Viola Devasirvatham ◽  
Pooran M. Gaur ◽  
Nalini Mallikarjuna ◽  
Raju N. Tokachichu ◽  
Richard M. Trethowan ◽  
...  
Keyword(s):  
Heat Stress ◽  
High Temperature ◽  
Pollen Germination ◽  
Pollen Viability ◽  
Pollen Grains ◽  
High Temperature Stress ◽  
Pollen Production ◽  
Seed Number ◽  
Controlled Environments

High temperature during the reproductive stage in chickpea (Cicer arietinum L.) is a major cause of yield loss. The objective of this research was to determine whether that variation can be explained by differences in anther and pollen development under heat stress: the effect of high temperature during the pre- and post-anthesis periods on pollen viability, pollen germination in a medium, pollen germination on the stigma, pollen tube growth and pod set in a heat-tolerant (ICCV 92944) and a heat-sensitive (ICC 5912) genotype was studied. The plants were evaluated under heat stress and non-heat stress conditions in controlled environments. High temperature stress (29/16°C to 40/25°C) was gradually applied at flowering to study pollen viability and stigma receptivity including flower production, pod set and seed number. This was compared with a non-stress treatment (27/16°C). The high temperatures reduced pod set by reducing pollen viability and pollen production per flower. The ICCV 92944 pollen was viable at 35/20°C (41% fertile) and at 40/25°C (13% fertile), whereas ICC 5912 pollen was completely sterile at 35/20°C with no in vitro germination and no germination on the stigma. However, the stigma of ICC 5912 remained receptive at 35/20°C and non-stressed pollen (27/16°C) germinated on it during reciprocal crossing. These data indicate that pollen grains were more sensitive to high temperature than the stigma in chickpea. High temperature also reduced pollen production per flower, % pollen germination, pod set and seed number.

scholarly journals Overexpression of Two CCCH-type Zinc-Finger Protein Genes Leads to Pollen Abortion in Brassica campestris ssp. chinensis

Genes ◽  
2020 ◽  
Vol 11 (11) ◽  
pp. 1287
Author(s):  
Liai Xu ◽  
Tingting Liu ◽  
Xingpeng Xiong ◽  
Weimiao Liu ◽  
Youjian Yu ◽  
...  
Keyword(s):  
Transgenic Plants ◽  
Zinc Finger ◽  
Pollen Development ◽  
Brassica Campestris ◽  
Zinc Finger Protein ◽  
Function Analysis ◽  
Pollen Grains ◽  
Functional Redundancy ◽  
Pollen Abortion ◽  
Finger Protein

The pollen grains produced by flowering plants are vital for sexual reproduction. Previous studies have shown that two CCCH-type zinc-finger protein genes in Brassica campestris, BcMF30a and BcMF30c, are involved in pollen development. Due to their possible functional redundancy, gain-of-function analysis is helpful to reveal their respective biological functions. Here, we found that the phenotypes of BcMF30a and BcMF30c overexpression transgenic plants driven by their native promoters were similar, suggesting their functional redundancy. The results showed that the vegetative growth was not affected in both transgenic plants, but male fertility was reduced. Further analysis found that the abortion of transgenic pollen was caused by the degradation of pollen contents from the late uninucleate microspore stage. Subcellular localization analysis demonstrated that BcMF30a and BcMF30c could localize in cytoplasmic foci. Combined with the studies of other CCCH-type genes, we speculated that the overexpression of these genes can induce the continuous assembly of abnormal cytoplasmic foci, thus resulting in defective plant growth and development, which, in this study, led to pollen abortion. Both the overexpression and knockout of BcMF30a and BcMF30c lead to abnormal pollen development, indicating that the appropriate expression levels of these two genes are critical for the maintenance of normal pollen development.

scholarly journals Identification of four unconventional kinetoplastid kinetochore proteins KKT22–25 in Trypanosoma brucei

Open Biology ◽  
2019 ◽  
Vol 9 (12) ◽  
pp. 190236 ◽  
Author(s):  
Olga O. Nerusheva ◽  
Patryk Ludzia ◽  
Bungo Akiyoshi
Keyword(s):  
Trypanosoma Brucei ◽  
Chromosome Segregation ◽  
Rna Binding ◽  
Affinity Purification ◽  
Potential Interaction ◽  
Interacting Proteins ◽  
Interaction Partners ◽  
Spindle Microtubules ◽  
Acetyltransferase Domain ◽  
Mitosis And Meiosis

The kinetochore is a multi-protein complex that drives chromosome segregation in eukaryotes. It assembles onto centromere DNA and interacts with spindle microtubules during mitosis and meiosis. Although most eukaryotes have canonical kinetochore proteins, kinetochores of evolutionarily divergent kinetoplastid species consist of at least 20 unconventional kinetochore proteins (KKT1–20). In addition, 12 proteins (KKT-interacting proteins 1–12, KKIP1–12) are known to localize at kinetochore regions during mitosis. It remains unclear whether KKIP proteins interact with KKT proteins. Here, we report the identification of four additional kinetochore proteins, KKT22–25, in Trypanosoma brucei . KKT22 and KKT23 constitutively localize at kinetochores, while KKT24 and KKT25 localize from S phase to anaphase. KKT23 has a Gcn5-related N -acetyltransferase domain, which is not found in any kinetochore protein known to date. We also show that KKIP1 co-purifies with KKT proteins, but not with KKIP proteins. Finally, our affinity purification of KKIP2/3/4/6 identifies a number of proteins as their potential interaction partners, many of which are implicated in RNA binding or processing. These findings further support the idea that kinetoplastid kinetochores are unconventional.

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