scholarly journals Editorial: Apoptosis and Senescence in Vertebrate Development

2022 ◽  
Vol 9 ◽  
Author(s):  
Wolfgang Knabe ◽  
Stefan Washausen
Keyword(s):  
Vertebrate Development

scholarly journals Biology and Physics of Heterochromatin-Like Domains/Complexes

Cells ◽  
2020 ◽  
Vol 9 (8) ◽  
pp. 1881
Author(s):  
Prim B. Singh ◽  
Stepan N. Belyakin ◽  
Petr P. Laktionov
Keyword(s):  
Phase Separation ◽  
Fission Yeast ◽  
Thermodynamic Description ◽  
Dynamic Structure ◽  
Vertebrate Development ◽  
Type Region ◽  
Additional Tool ◽  
3D Genome ◽  
Chromatin Template ◽  
Cis And Trans

The hallmarks of constitutive heterochromatin, HP1 and H3K9me2/3, assemble heterochromatin-like domains/complexes outside canonical constitutively heterochromatic territories where they regulate chromatin template-dependent processes. Domains are more than 100 kb in size; complexes less than 100 kb. They are present in the genomes of organisms ranging from fission yeast to human, with an expansion in size and number in mammals. Some of the likely functions of domains/complexes include silencing of the donor mating type region in fission yeast, preservation of DNA methylation at imprinted germline differentially methylated regions (gDMRs) and regulation of the phylotypic progression during vertebrate development. Far cis- and trans-contacts between micro-phase separated domains/complexes in mammalian nuclei contribute to the emergence of epigenetic compartmental domains (ECDs) detected in Hi-C maps. A thermodynamic description of micro-phase separation of heterochromatin-like domains/complexes may require a gestalt shift away from the monomer as the “unit of incompatibility” that determines the sign and magnitude of the Flory–Huggins parameter, χ. Instead, a more dynamic structure, the oligo-nucleosomal “clutch”, consisting of between 2 and 10 nucleosomes is both the long sought-after secondary structure of chromatin and its unit of incompatibility. Based on this assumption we present a simple theoretical framework that enables an estimation of χ for domains/complexes flanked by euchromatin and thereby an indication of their tendency to phase separate. The degree of phase separation is specified by χN, where N is the number of “clutches” in a domain/complex. Our approach could provide an additional tool for understanding the biophysics of the 3D genome.

scholarly journals Second-order division in sectors as a prepattern for sensory organs in vertebrate development

2021 ◽  
Author(s):  
Vincent Fleury ◽  
Alexis Peaucelle ◽  
Anick Abourachid ◽  
Olivia Plateau
Keyword(s):  
Second Order ◽  
Vertebrate Development ◽  
Sensory Organs

scholarly journals PLRG1 Is an Essential Regulator of Cell Proliferation and Apoptosis during Vertebrate Development and Tissue Homeostasis

2009 ◽  
Vol 29 (11) ◽  
pp. 3173-3185 ◽  
Author(s):  
André Kleinridders ◽  
Hans-Martin Pogoda ◽  
Sigrid Irlenbusch ◽  
Neil Smyth ◽  
Csaba Koncz ◽  
...  
Keyword(s):  
Cell Cycle Progression ◽  
Tissue Homeostasis ◽  
Mrna Splicing ◽  
Vertebrate Development ◽  
Adult Tissue ◽  
Serum Stimulation ◽  
Evolutionarily Conserved ◽  
Proliferation And Apoptosis ◽  
Dependent Cell

ABSTRACT PLRG1, an evolutionarily conserved component of the spliceosome, forms a complex with Pso4/SNEV/Prp19 and the cell division and cycle 5 homolog (CDC5L) that is involved in both pre-mRNA splicing and DNA repair. Here, we show that the inactivation of PLRG1 in mice results in embryonic lethality at 1.5 days postfertilization. Studies of heart- and neuron-specific PLRG1 knockout mice further reveal an essential role of PLRG1 in adult tissue homeostasis and the suppression of apoptosis. PLRG1-deficient mouse embryonic fibroblasts (MEFs) fail to progress through S phase upon serum stimulation and exhibit increased rates of apoptosis. PLRG1 deficiency causes enhanced p53 phosphorylation and stabilization in the presence of increased γ-H2AX immunoreactivity as an indicator of an activated DNA damage response. p53 downregulation rescues lethality in both PLRG1-deficient MEFs and zebrafish in vivo, showing that apoptosis resulting from PLRG1 deficiency is p53 dependent. Moreover, the deletion of PLRG1 results in the relocation of its interaction partner CDC5L from the nucleus to the cytoplasm without general alterations in pre-mRNA splicing. Taken together, the results of this study identify PLRG1 as a critical nuclear regulator of p53-dependent cell cycle progression and apoptosis during both embryonic development and adult tissue homeostasis.

Protein partners of KCTD proteins provide insights about their functional roles in cell differentiation and vertebrate development

BioEssays ◽  
2013 ◽  
Vol 35 (7) ◽  
pp. 586-596 ◽  
Author(s):  
Mikhail Skoblov ◽  
Andrey Marakhonov ◽  
Ekaterina Marakasova ◽  
Anna Guskova ◽  
Vikas Chandhoke ◽  
...  
Keyword(s):  
Cell Differentiation ◽  
Vertebrate Development ◽  
Functional Roles ◽  
Protein Partners

T-Box Genes in Vertebrate Development

2005 ◽  
Vol 39 (1) ◽  
pp. 219-239 ◽  
Author(s):  
L.A. Naiche ◽  
Zachary Harrelson ◽  
Robert G. Kelly ◽  
Virginia E. Papaioannou
Keyword(s):  
Vertebrate Development ◽  
T Box
Sign in / Sign up

Export Citation Format

Share Document