Expression of senescence in Neurospora intermedia

1986 ◽  
Vol 28 (3) ◽  
pp. 459-467 ◽  
Author(s):  
A. J. F. Griffiths ◽  
S. Kraus ◽  
H. Bertrand

Kalilo cytoplasms of Neurospora intermedia have been shown to express senescence in two ways. First, by the previously reported way of death in a subculture series, and second, as reported here, by growth cessation in a 50-cm race tube. Only those cultures that are sufficiently far advanced in the development of senescence will stop growth in the length of a race tube. Resumption of growth occurs in most cases of growth arrest in race tubes. Although in subculture series growth resumption is rare, there is probably a similar basis: mitochondrial DNA (mtDNA) studies on one such case showed that growth resumption is associated with a resurgence of normal mtDNA and a decline of abnormal genomes. When senescent cultures in race tubes were sampled by removing mycelial cores, longer grown cultures were shown to be able to support less growth than younger cultures of the same genotype, and the growth front was generally able to support less growth than other regions. Therefore senescence in both transfer series and in race tubes involves the accumulation of genetic factors unable to suppport continuous growth. The expression of senescence is considered to be more efficient in subculture series than in race tubes. In such series, conidia or aerial hyphae work equally well as transfer inocula, but 1-mm hyphal tips cut from growing mycelium do not promote senescence when used as inocula. Furthermore, varying the transfer interval does not affect senescence. It is concluded that there is some feature of the development or germination of quiescent cells that enhances the expression of senescence in Neurospora.Key words: Neurospora, senescence, mitochondria, growth.

2011 ◽  
Vol 30 (9) ◽  
pp. 681-689 ◽  
Author(s):  
Viola Breyer ◽  
Cord-Michael Becker ◽  
Monika Pischetsrieder

2020 ◽  
Author(s):  
Jesse Slone ◽  
Weiwei Zou ◽  
Shiyu Luo ◽  
Eric S Schmitt ◽  
Stella Maris Chen ◽  
...  

ABSTRACTWith very few exceptions, mitochondrial DNA (mtDNA) in humans is transmitted exclusively from mothers to their offspring, suggesting the presence of a strong evolutionary pressure favoring the exclusion of paternal mtDNA. We have recently shown strong evidence of paternal mtDNA transmission. In these rare situations, males exhibiting biparental mtDNA appear to be limited to transmitting just one of the mtDNA species to their offspring, while females possessing biparental mtDNA populations consistently transmit both populations to their offspring at a very similar heteroplasmy level. The precise biological and genetic factors underlying this unusual transmission event remain unclear. Here, we have examined heteroplasmy levels in various tissues among individuals with biparental inheritance. Our results indicate that individuals with biparental mtDNA have remarkable inter-tissue variability in heteroplasmy level. At the single-cell level, paternal mtDNA heteroplasmy in sperm varies dramatically, and many sperm possess only one of the two mtDNA populations originally in question. These results show a fundamental, parent-of-origin difference in how mtDNA molecules transmit and propagate. This helps explain how a single population of mtDNAs are transmitted from a father possessing two populations of mtDNA molecules, suggesting that some mtDNA populations may be favored over others when transmitted from the father.


1998 ◽  
Vol 18 (6) ◽  
pp. 3163-3172 ◽  
Author(s):  
Muthupalaniappan Meyyappan ◽  
Howard Wong ◽  
Christopher Hull ◽  
Karl T. Riabowol

ABSTRACT Cyclin D2 is a member of the family of D-type cyclins that is implicated in cell cycle regulation, differentiation, and oncogenic transformation. To better understand the role of this cyclin in the control of cell proliferation, cyclin D2 expression was monitored under various growth conditions in primary human and established murine fibroblasts. In different states of cellular growth arrest initiated by contact inhibition, serum starvation, or cellular senescence, marked increases (5- to 20-fold) were seen in the expression levels of cyclin D2 mRNA and protein. Indirect immunofluorescence studies showed that cyclin D2 protein localized to the nucleus in G0, suggesting a nuclear function for cyclin D2 in quiescent cells. Cyclin D2 was also found to be associated with the cyclin-dependent kinases CDK2 and CDK4 but not CDK6 during growth arrest. Cyclin D2-CDK2 complexes increased in amounts but were inactive as histone H1 kinases in quiescent cells. Transient transfection and needle microinjection of cyclin D2 expression constructs demonstrated that overexpression of cyclin D2 protein efficiently inhibited cell cycle progression and DNA synthesis. These data suggest that in addition to a role in promoting cell cycle progression through phosphorylation of retinoblastoma family proteins in some cell systems, cyclin D2 may contribute to the induction and/or maintenance of a nonproliferative state, possibly through sequestration of the CDK2 catalytic subunit.


2021 ◽  
Vol 4 (1) ◽  
Author(s):  
Karla Santos-de-Frutos ◽  
Nabil Djouder

AbstractTumour recurrence is a serious impediment to cancer treatment, but the mechanisms involved are poorly understood. The most frequently used anti-tumour therapies—chemotherapy and radiotherapy—target highly proliferative cancer cells. However non- or slow-proliferative dormant cancer cells can persist after treatment, eventually causing tumour relapse. Whereas the reversible growth arrest mechanism allows quiescent cells to re-enter the cell cycle, senescent cells are largely thought to be irreversibly arrested, and may instead contribute to tumour growth and relapse through paracrine signalling mechanisms. Thus, due to the differences in their growth arrest mechanism, metabolic features, plasticity and adaptation to their respective tumour microenvironment, dormant-senescent and -quiescent cancer cells could have different but complementary roles in fuelling tumour growth. In this review article, we discuss the implication of dormant cancer cells in tumour relapse and the need to understand how quiescent and senescent cells, respectively, may play a part in this process.


Development ◽  
2001 ◽  
Vol 128 (2) ◽  
pp. 243-252 ◽  
Author(s):  
V. Raz ◽  
J.H. Bergervoet ◽  
M. Koornneef

The continuous growth of the plant embryo is interrupted during the seed maturation processes which results in a dormant seed. The embryo continues development after germination when it grows into a seedling. The embryo growth phase starts after morphogenesis and ends when the embryo fills the seed sac. Very little is known about the processes regulating this phase. We describe mutants that affect embryo growth in two sequential developmental stages. Firstly, embryo growth arrest is regulated by the FUS3/LEC type genes, as mutations in these genes cause a continuation of growth in immature embryos. Secondly, a later stage of embryo dormancy is regulated by ABI3 and abscisic acid; abi3 and aba1 mutants exhibit premature germination only after embryos mature. Mutations affecting both developmental stages result in an additive phenotype and double mutants are highly viviparous. Embryo growth arrest is regulated by cell division activities in both the embryo and the endosperm, which are gradually switched off at the mature embryo stage. In the fus3/lec mutants, however, cell division in both the embryo and endosperm is not arrested, but rather is prolonged throughout seed maturation. Furthermore ectopic cell division occurs in seedlings. Our results indicate that seed dormancy is secured via at least two sequential developmental processes: embryo growth arrest, which is regulated by cell division and embryo dormancy.


2007 ◽  
Vol 546-549 ◽  
pp. 2091-2096
Author(s):  
Hai Tao Cao ◽  
Rui Hu ◽  
Hong Chao Kou ◽  
Jin Shan Li ◽  
En Zhi Gao ◽  
...  

The unidirectional solidification technology by a zone melting method was performed to obtain the large single domain YBCO. The interface morphology and chemical composition at the growth front of the YBCO crystal were investigated in order to make clear the growth characteristic of the YBCO crystal during melting growth by unidirectional solidification. It was found that YBCO crystal would cease growing when yttrium was depleted in the liquid phase at the YBCO crystal growth front. For maintaining the continuous growth of YBCO crystal, compositions of Y, Ba and Cu in raw samples have to be adjusted so as to make yttrium rich in the liquid phase at the YBCO crystal growth front during the melting growth process. It is very useful for the study on the mechanism of the YBCO crystal growth.


2017 ◽  
Vol 114 (48) ◽  
pp. E10329-E10338 ◽  
Author(s):  
Tian Zhang ◽  
Clara Wolfe ◽  
Andrew Pierle ◽  
Kevin A. Welle ◽  
Jennifer R. Hryhorenko ◽  
...  

In dividing cells, cytoplasmic dilution is the dominant route of clearance for long-lived proteins whose inherent degradation is slower than the cellular growth rate. Thus, as cells transition from a dividing to a nondividing state, there is a propensity for long-lived proteins to become stabilized relative to short-lived proteins, leading to alterations in the abundance distribution of the proteome. However, it is not known if cells mount a compensatory response to counter this potentially deleterious proteostatic disruption. We used a proteomic approach to demonstrate that fibroblasts selectively increase degradation rates of long-lived proteins as they transition from a proliferating to a quiescent state. The selective degradation of long-lived proteins occurs by the concurrent activation of lysosomal biogenesis and up-regulation of macroautophagy. Through this mechanism, quiescent cells avoid the accumulation of aged long-lived proteins that would otherwise result from the absence of cytoplasmic dilution by cell division.


Author(s):  
C. M. Chun ◽  
A. Navrotsky ◽  
I. A. Aksay

Nanocrystalline BaTiO3 particles are synthesized under hydrothermal conditions by the reaction of nanosized TiO2 colloids with aqueous solutions of Ba(OH)2 at 80°C. A dissolution-precipitation mechanism is proposed for the formation of BaTiOs by this route, because suspended TiO2 nano-particles dissolve into Ba(OH)2 solution, supersaturate the solution phase, and subsequently precipitate BaTiOs particles. The origin of the rough "raspberry-like" BaTiOs particles during growth stages can be explained by one of two mechanisms: (i) the morphological instability at the growth front during continuous growth, or (ii) aggregation of colloidal particles by multiple clustering. Our TEM studies on samples prepared by controlled seeding experiments show that a multiplicity of low or high angle grain boundaries occur during growth, supporting the aggregation growth.In order to separate the nucleation step from the growth step more efficiently, seed BaTiO3 particles were prepared by adding TiO2 colloids (Degussa, P-25) to 2.23 M Ba(OH)2 solution and hydrothermally reacting at 80°C under atmospheric pressure for 48 hours in polyethylene bottles. The resulting seed particles were recovered by centrifugation, rinsed with C02-free deionized water and freeze-dried.


Sign in / Sign up

Export Citation Format

Share Document