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2.
Curr Top Dev Biol ; 159: 1-27, 2024.
Article in English | MEDLINE | ID: mdl-38729674

ABSTRACT

The diversity of vertebrate body plans is dizzying, yet stunning for the many things they have in common. Vertebrates have inhabited virtually every part of the earth from its coldest to warmest climates. They locomote by swimming, flying, walking, slithering, or climbing, or combinations of these behaviors. And they exist in many different sizes, from the smallest of frogs, fish and lizards to giraffes, elephants, and blue whales. Despite these differences, vertebrates follow a remarkably similar blueprint for the establishment of their body plan. Within the relatively small amount of time required to complete gastrulation, the process through which the three germ layers, ectoderm, mesoderm, and endoderm are created, the embryo also generates its body axis and is simultaneously patterned. For the length of this axis, the genes that distinguish the neck from the rib cage or the trunk from the sacrum are the Hox genes. In vertebrates, there was evolutionary pressure to maintain this set of genes in the organism. Over the past decades, much has been learned regarding the regulatory mechanisms that ensure the appropriate expression of these genes along the main body axes. Genetic functions continue to be explored though much has been learned. Much less has been discerned on the identity of co-factors used by Hox proteins for the specificity of transcriptional regulation or what downstream targets and pathways are critical for patterning events, though there are notable exceptions. Current work in the field is demonstrating that Hox genes continue to function in many organs long after directing early patterning events. It is hopeful continued research will shed light on remaining questions regarding mechanisms used by this important and conserved set of transcriptional regulators.


Subject(s)
Body Patterning , Gene Expression Regulation, Developmental , Genes, Homeobox , Vertebrates , Animals , Body Patterning/genetics , Vertebrates/genetics , Vertebrates/embryology , Genes, Homeobox/genetics
3.
Curr Top Dev Biol ; 159: 272-308, 2024.
Article in English | MEDLINE | ID: mdl-38729678

ABSTRACT

Although vertebrates display a large variety of forms and sizes, the mechanisms controlling the layout of the basic body plan are substantially conserved throughout the clade. Following gastrulation, head, trunk, and tail are sequentially generated through the continuous addition of tissue at the caudal embryonic end. Development of each of these major embryonic regions is regulated by a distinct genetic network. The transitions from head-to-trunk and from trunk-to-tail development thus involve major changes in regulatory mechanisms, requiring proper coordination to guarantee smooth progression of embryonic development. In this review, we will discuss the key cellular and embryological events associated with those transitions giving particular attention to their regulation, aiming to provide a cohesive outlook of this important component of vertebrate development.


Subject(s)
Body Patterning , Gene Expression Regulation, Developmental , Animals , Humans , Embryonic Development , Gastrulation , Vertebrates/embryology
4.
Philos Trans R Soc Lond B Biol Sci ; 379(1905): 20230204, 2024 Jul 08.
Article in English | MEDLINE | ID: mdl-38768211

ABSTRACT

To receive the benefits of social living, individuals must make effective group decisions that enable them to achieve behavioural coordination and maintain cohesion. However, heterogeneity in the physical and social environments surrounding group decision-making contexts can increase the level of difficulty social organisms face in making decisions. Groups that live in variable physical environments (high ecological heterogeneity) can experience barriers to information transfer and increased levels of ecological uncertainty. In addition, in groups with large phenotypic variation (high individual heterogeneity), individuals can have substantial conflicts of interest regarding the timing and nature of activities, making it difficult for them to coordinate their behaviours or reach a consensus. In such cases, active communication can increase individuals' abilities to achieve coordination, such as by facilitating the transfer and aggregation of information about the environment or individual behavioural preferences. Here, we review the role of communication in vertebrate group decision-making and its relationship to heterogeneity in the ecological and social environment surrounding group decision-making contexts. We propose that complex communication has evolved to facilitate decision-making in specific socio-ecological contexts, and we provide a framework for studying this topic and testing related hypotheses as part of future research in this area. This article is part of the theme issue 'The power of sound: unravelling how acoustic communication shapes group dynamics'.


Subject(s)
Decision Making , Social Behavior , Animals , Vertebrates/physiology , Animal Communication
6.
Curr Top Dev Biol ; 159: 310-342, 2024.
Article in English | MEDLINE | ID: mdl-38729680

ABSTRACT

External bilateral symmetry is a prevalent feature in vertebrates, which emerges during early embryonic development. To begin with, vertebrate embryos are largely radially symmetric before transitioning to bilaterally symmetry, after which, morphogenesis of various bilateral tissues (e.g somites, otic vesicle, limb bud), and structures (e.g palate, jaw) ensue. While a significant amount of work has probed the mechanisms behind symmetry breaking in the left-right axis leading to asymmetric positioning of internal organs, little is known about how bilateral tissues emerge at the same time with the same shape and size and at the same position on the two sides of the embryo. By discussing emergence of symmetry in many bilateral tissues and structures across vertebrate model systems, we highlight that understanding symmetry establishment is largely an open field, which will provide deep insights into fundamental problems in developmental biology for decades to come.


Subject(s)
Body Patterning , Vertebrates , Animals , Vertebrates/embryology , Embryonic Development , Gene Expression Regulation, Developmental , Morphogenesis , Somites/embryology
7.
Curr Top Dev Biol ; 159: 30-58, 2024.
Article in English | MEDLINE | ID: mdl-38729679

ABSTRACT

Morphogenesis from cells to tissue gives rise to the complex architectures that make our organs. How cells and their dynamic behavior are translated into functional spatial patterns is only starting to be understood. Recent advances in quantitative imaging revealed that, although highly heterogeneous, cellular behaviors make reproducible tissue patterns. Emerging evidence suggests that mechanisms of cellular coordination, intrinsic variability and plasticity are critical for robust pattern formation. While pattern development shows a high level of fidelity, tissue organization has undergone drastic changes throughout the course of evolution. In addition, alterations in cell behavior, if unregulated, can cause developmental malformations that disrupt function. Therefore, comparative studies of different species and of disease models offer a powerful approach for understanding how novel spatial configurations arise from variations in cell behavior and the fundamentals of successful pattern formation. In this chapter, I dive into the development of the vertebrate nervous system to explore efforts to dissect pattern formation beyond molecules, the emerging core principles and open questions.


Subject(s)
Nervous System , Vertebrates , Animals , Vertebrates/physiology , Vertebrates/embryology , Nervous System/growth & development , Nervous System/embryology , Body Patterning , Humans , Morphogenesis
8.
Curr Top Dev Biol ; 159: 132-167, 2024.
Article in English | MEDLINE | ID: mdl-38729675

ABSTRACT

The primary senses-touch, taste, sight, smell, and hearing-connect animals with their environments and with one another. Aside from the eyes, the primary sense organs of vertebrates and the peripheral sensory pathways that relay their inputs arise from two transient stem cell populations: the neural crest and the cranial placodes. In this chapter we consider the senses from historical and cultural perspectives, and discuss the senses as biological faculties. We begin with the embryonic origin of the neural crest and cranial placodes from within the neural plate border of the ectodermal germ layer. Then, we describe the major chemical (i.e. olfactory and gustatory) and mechanical (i.e. vestibulo-auditory and somatosensory) senses, with an emphasis on the developmental interactions between neural crest and cranial placodes that shape their structures and functions.


Subject(s)
Neural Crest , Animals , Neural Crest/cytology , Neural Crest/embryology , Neural Crest/physiology , Humans , Sensation/physiology , Sense Organs/embryology , Sense Organs/physiology , Sense Organs/cytology , Vertebrates/embryology , Vertebrates/physiology
9.
Anat Histol Embryol ; 53(3): e13052, 2024 May.
Article in English | MEDLINE | ID: mdl-38735035

ABSTRACT

One crucial component of the optical system is the ciliary body (CB). This body secretes the aqueous humour, which is essential to maintain the internal eye pressure as well as the clearness of the lens and cornea. The histological study was designed to provide the morphological differences of CB and iris in the anterior eye chambers of the following vertebrate classes: fish (grass carp), amphibians (Arabian toad), reptiles (semiaquatic turtle, fan-footed gecko, ocellated skink, Egyptian spiny-tailed lizard, Arabian horned viper), birds (common pigeon, common quail, common kestrel), and mammals (BALB/c mouse, rabbit, golden hamster, desert hedgehog, lesser Egyptian jerboa, Egyptian fruit bat). The results showed distinct morphological appearances of the CB and iris in each species, ranging from fish to mammals. The present comparative study concluded that the morphological structure of the CB and iris is the adaptation of species to either their lifestyle or survival in specific habitats.


Subject(s)
Ciliary Body , Iris , Animals , Ciliary Body/anatomy & histology , Iris/anatomy & histology , Rabbits/anatomy & histology , Mice/anatomy & histology , Lizards/anatomy & histology , Vertebrates/anatomy & histology , Reptiles/anatomy & histology , Fishes/anatomy & histology , Birds/anatomy & histology , Anterior Chamber/anatomy & histology , Turtles/anatomy & histology , Carps/anatomy & histology , Mice, Inbred BALB C , Amphibians/anatomy & histology , Cricetinae , Quail/anatomy & histology , Hedgehogs/anatomy & histology , Columbidae/anatomy & histology , Mesocricetus/anatomy & histology
10.
Genome Biol ; 25(1): 120, 2024 May 13.
Article in English | MEDLINE | ID: mdl-38741126

ABSTRACT

BACKGROUND: Genomic regions that remain poorly understood, often referred to as the dark genome, contain a variety of functionally relevant and biologically informative features. These include endogenous viral elements (EVEs)-virus-derived sequences that can dramatically impact host biology and serve as a virus fossil record. In this study, we introduce a database-integrated genome screening (DIGS) approach to investigate the dark genome in silico, focusing on EVEs found within vertebrate genomes. RESULTS: Using DIGS on 874 vertebrate genomes, we uncover approximately 1.1 million EVE sequences, with over 99% originating from endogenous retroviruses or transposable elements that contain EVE DNA. We show that the remaining 6038 sequences represent over a thousand distinct horizontal gene transfer events across 10 virus families, including some that have not previously been reported as EVEs. We explore the genomic and phylogenetic characteristics of non-retroviral EVEs and determine their rates of acquisition during vertebrate evolution. Our study uncovers novel virus diversity, broadens knowledge of virus distribution among vertebrate hosts, and provides new insights into the ecology and evolution of vertebrate viruses. CONCLUSIONS: We comprehensively catalog and analyze EVEs within 874 vertebrate genomes, shedding light on the distribution, diversity, and long-term evolution of viruses and reveal their extensive impact on vertebrate genome evolution. Our results demonstrate the power of linking a relational database management system to a similarity search-based screening pipeline for in silico exploration of the dark genome.


Subject(s)
Fossils , Genome , Phylogeny , Vertebrates , Animals , Vertebrates/genetics , Vertebrates/virology , Evolution, Molecular , Humans , Gene Transfer, Horizontal , Viruses/genetics , Genomics/methods , Endogenous Retroviruses/genetics , DNA Transposable Elements
11.
Commun Biol ; 7(1): 612, 2024 May 21.
Article in English | MEDLINE | ID: mdl-38773256

ABSTRACT

The telencephalon has undergone remarkable diversification and expansion throughout vertebrate evolution, exhibiting striking variations in structural and functional complexity. Nevertheless, fundamental features are shared across vertebrate taxa, such as the presence of distinct regions including the pallium, subpallium, and olfactory structures. Teleost fishes have a uniquely "everted" telencephalon, which has confounded comparisons of their brain regions to other vertebrates. Here we combine spatial transcriptomics and single nucleus RNA-sequencing to generate a spatially-resolved transcriptional atlas of the Mchenga conophorus cichlid fish telencephalon. We then compare cell-types and anatomical regions in the cichlid telencephalon with those in amphibians, reptiles, birds, and mammals. We uncover striking transcriptional similarities between cell-types in the fish telencephalon and subpallial, hippocampal, and cortical cell-types in tetrapods, and find support for partial eversion of the teleost telencephalon. Ultimately, our work lends new insights into the organization and evolution of conserved cell-types and regions in the vertebrate forebrain.


Subject(s)
Cichlids , Prosencephalon , Telencephalon , Animals , Telencephalon/cytology , Prosencephalon/cytology , Cichlids/genetics , Transcriptome , Vertebrates/genetics , Biological Evolution
12.
Proc Natl Acad Sci U S A ; 121(24): e2318189121, 2024 Jun 11.
Article in English | MEDLINE | ID: mdl-38814876

ABSTRACT

Fluorescence, the optical phenomenon whereby short-wavelength light is absorbed and emitted at longer wavelengths, has been widely described in aquatic habitats, in both invertebrates and fish. Recent years have seen a stream of articles reporting fluorescence, ranging from frogs, platypus, to even fully terrestrial organisms such as flying squirrels, often explicitly or implicitly linking the presence of fluorescence with sexual selection and communication. However, many of these studies fail to consider the physiological requirements of evolutionary stable signaling systems, the environmental dependence of perception, or the possible adaptive role of fluorescent coloration in a noncommunicative context. More importantly, the idea that fluorescence may simply constitute an indirect by-product of selection on other traits is often not explored. This is especially true for terrestrial systems where environmental light conditions are often not amenable for fluorescent signaling in contrast to, for example, aquatic habitats in which spectral properties of water promote functional roles for fluorescence. Despite the appeal of previously unknown ways in which coloration may drive evolution, the investigation of a putative role of fluorescence in communication must be tempered by a realistic understanding of its limitations. Here, we not only highlight and discuss the key body of literature but also address the potential pitfalls when reporting fluorescence and how to solve them. In addition, we propose exciting different research avenues to advance the field of tetrapod fluorescence.


Subject(s)
Biological Evolution , Animals , Fluorescence , Vertebrates/physiology , Animal Communication , Ecosystem
13.
Sci Rep ; 14(1): 10624, 2024 05 09.
Article in English | MEDLINE | ID: mdl-38724555

ABSTRACT

To date, the presence of pulmonary organs in the fossil record is extremely rare. Among extant vertebrates, lungs are described in actinopterygian polypterids and in all sarcopterygians, including coelacanths and lungfish. However, vasculature of pulmonary arteries has never been accurately identified neither in fossil nor extant coelacanths due to the paucity of fossil preservation of pulmonary organs and limitations of invasive studies in extant specimens. Here we present the first description of the pulmonary vasculature in both fossil and extant actinistian, a non-tetrapod sarcopterygian clade, contributing to a more in-depth discussion on the morphology of these structures and on the possible homology between vertebrate air-filled organs (lungs of sarcopterygians, lungs of actinopterygians, and gas bladders of actinopterygians).


Subject(s)
Biological Evolution , Fishes , Fossils , Pulmonary Artery , Animals , Pulmonary Artery/anatomy & histology , Fishes/anatomy & histology , Vertebrates/anatomy & histology , Lung/blood supply , Phylogeny
14.
Nat Commun ; 15(1): 4550, 2024 May 29.
Article in English | MEDLINE | ID: mdl-38811547

ABSTRACT

The emergence of new structures can often be linked to the evolution of novel cell types that follows the rewiring of developmental gene regulatory subnetworks. Vertebrates are characterized by a complex body plan compared to the other chordate clades and the question remains of whether and how the emergence of vertebrate morphological innovations can be related to the appearance of new embryonic cell populations. We previously proposed, by studying mesoderm development in the cephalochordate amphioxus, a scenario for the evolution of the vertebrate head mesoderm. To further test this scenario at the cell population level, we used scRNA-seq to construct a cell atlas of the amphioxus neurula, stage at which the main mesodermal compartments are specified. Our data allowed us to validate the presence of a prechordal-plate like territory in amphioxus. Additionally, the transcriptomic profile of somite cell populations supports the homology between specific territories of amphioxus somites and vertebrate cranial/pharyngeal and lateral plate mesoderm. Finally, our work provides evidence that the appearance of the specific mesodermal structures of the vertebrate head was associated to both segregation of pre-existing cell populations, and co-option of new genes for the control of myogenesis.


Subject(s)
Gene Expression Regulation, Developmental , Head , Lancelets , Mesoderm , Vertebrates , Animals , Mesoderm/cytology , Mesoderm/embryology , Lancelets/embryology , Lancelets/genetics , Head/embryology , Vertebrates/embryology , Vertebrates/genetics , Somites/embryology , Somites/cytology , Somites/metabolism , Biological Evolution , Transcriptome
15.
Immunity ; 57(4): 613-631, 2024 Apr 09.
Article in English | MEDLINE | ID: mdl-38599162

ABSTRACT

While largely neglected over decades during which adaptive immunity captured most of the attention, innate immune mechanisms have now become central to our understanding of immunology. Innate immunity provides the first barrier to infection in vertebrates, and it is the sole mechanism of host defense in invertebrates and plants. Innate immunity also plays a critical role in maintaining homeostasis, shaping the microbiota, and in disease contexts such as cancer, neurodegeneration, metabolic syndromes, and aging. The emergence of the field of innate immunity has led to an expanded view of the immune system, which is no longer restricted to vertebrates and instead concerns all metazoans, plants, and even prokaryotes. The study of innate immunity has given rise to new concepts and language. Here, we review the history and definition of the core concepts of innate immunity, discussing their value and fruitfulness in the long run.


Subject(s)
Immunity, Innate , Immunologic Memory , Animals , Invertebrates , Adaptive Immunity , Vertebrates
16.
Zoolog Sci ; 41(1): 77-86, 2024 Feb.
Article in English | MEDLINE | ID: mdl-38587520

ABSTRACT

Androgen(s) is one of the sex steroids that are involved in many physiological phenomena of vertebrate species. Although androgens were originally identified as male sex hormones, it is well known now that they are also essential in females. As in the case of other steroid hormones, androgen is produced from cholesterol through serial enzymatic reactions. Although testis is a major tissue to produce androgens in all species, androgens are also produced in ovary and adrenal (interrenal tissue). Testosterone is the most common and famous androgen. It represents a major androgen both in males and females of almost vertebrate species. In addition, testosterone is a precursor for producing significant androgens such as11-ketotestosterone, 5α-dihydrotestosterone, 11-ketodihydrotestosterones and 15α-hydroxytestosterone in a species- or sex-dependent manner for their homeostasis. In this article, we will review the significance and characteristics of these androgens, following a description of the history of testosterone discovery and its synthetic pathways.


Subject(s)
Androgens , Testosterone , Male , Animals , Female , Ovary , Testis , Vertebrates
17.
Zoolog Sci ; 41(1): 105-116, 2024 Feb.
Article in English | MEDLINE | ID: mdl-38587523

ABSTRACT

Melatonin (N-acetyl-5-methoxytryptamine) is an indolamine that is synthesized from tryptophan in the pineal glands of vertebrates through four enzymatic reactions. Melatonin is a quite unique bioactive substance, characterized by a combination of both receptor-mediated and receptor-independent actions, which promote the diverse effects of melatonin. One of the main functions of melatonin, via its membrane receptors, is to regulate the circadian or seasonal rhythm. In mammals, light information, which controls melatonin synthesis, is received in the eye, and transmitted to the pineal gland, via the suprachiasmatic nucleus, where the central clock is located. Alternatively, in many vertebrates other than mammals, the pineal gland cells, which are involved in melatonin synthesis and secretion and in the circadian clock, directly receive light. Recently, it has been reported that melatonin possesses several metabolic functions, which involve bone and glucose, in addition to regulating the circadian rhythm. Melatonin improves bone strength by inhibiting osteoclast activity. It is also known to maintain brain activity during sleep by increasing glucose uptake at night, in an insulin-independent manner. Moreover, as a non-receptor-mediated action, melatonin has antioxidant properties. Melatonin has been proven to be a potent free radical scavenger and a broad-spectrum antioxidant, even protecting organisms against radiation from space. Melatonin is a ubiquitously distributed molecule and is found in bacteria, unicellular organisms, fungi, and plants. It is hypothesized that melatonin initially functioned as an antioxidant, then, in vertebrates, it combined this role with the ability to regulate rhythm and metabolism, via its receptors.


Subject(s)
Circadian Clocks , Melatonin , Animals , Melatonin/pharmacology , Antioxidants , Vertebrates , Mammals
18.
Zoolog Sci ; 41(1): 132-139, 2024 Feb.
Article in English | MEDLINE | ID: mdl-38587526

ABSTRACT

Vertebrates have expanded their habitats during evolution, which accompanies diversified routes for water acquisition. Water is acquired by oral intake and subsequent absorption by the intestine in terrestrial and marine animals which are subjected to constant dehydration, whereas most water is gained osmotically across body surfaces in freshwater animals. In addition, a significant amount of water, called metabolic water, is produced within the body by the oxidation of hydrogen in organic substrates. The importance of metabolic water production as a strategy for water acquisition has been well documented in desert animals, but its role has attracted little attention in marine animals which also live in a dehydrating environment. In this article, the author has attempted to reevaluate the role of metabolic water production in body fluid regulation in animals inhabiting desiccating environments. Because of the exceptional ability of their kidney, marine mammals are thought to typically gain water by drinking environmental seawater and excreting excess NaCl in the urine. On the other hand, it is established that marine teleosts drink seawater to enable intestinal water and ion absorption, and the excess NaCl is excreted by branchial ionocytes. In addition to the oral route, we suggest through experiments using eels that water production by lipid metabolism is an additional route for water acquisition when they encounter seawater. It seems that metabolic water production contributes to counteract dehydration before mechanisms for water regulation are reversed from excretion in freshwater to acquisition in seawater.


Subject(s)
Dehydration , Water , Animals , Sodium Chloride , Seawater , Vertebrates , Mammals
19.
Sci Rep ; 14(1): 7690, 2024 04 02.
Article in English | MEDLINE | ID: mdl-38565870

ABSTRACT

Tunicates are evolutionary model organisms bridging the gap between vertebrates and invertebrates. A genomic sequence in Ciona intestinalis (CiOX) shows high similarity to vertebrate orexin receptors and protostome allatotropin receptors (ATR). Here, molecular phylogeny suggested that CiOX is divergent from ATRs and human orexin receptors (hOX1/2). However, CiOX appears closer to hOX1/2 than to ATR both in terms of sequence percent identity and in its modelled binding cavity, as suggested by molecular modelling. CiOX was heterologously expressed in a recombinant HEK293 cell system. Human orexins weakly but concentration-dependently activated its Gq signalling (Ca2+ elevation), and the responses were inhibited by the non-selective orexin receptor antagonists TCS 1102 and almorexant, but only weakly by the OX1-selective antagonist SB-334867. Furthermore, the 5-/6-carboxytetramethylrhodamine (TAMRA)-labelled human orexin-A was able to bind to CiOX. Database mining was used to predict a potential endogenous C. intestinalis orexin peptide (Ci-orexin-A). Ci-orexin-A was able to displace TAMRA-orexin-A, but not to induce any calcium response at the CiOX. Consequently, we suggested that the orexin signalling system is conserved in Ciona intestinalis, although the relevant peptide-receptor interaction was not fully elucidated.


Subject(s)
Ciona intestinalis , Animals , Humans , Orexin Receptors/genetics , Orexin Receptors/metabolism , Orexins/genetics , Orexins/metabolism , Ciona intestinalis/genetics , Ciona intestinalis/metabolism , HEK293 Cells , Signal Transduction , Vertebrates/metabolism , Carrier Proteins/metabolism
20.
Sci Rep ; 14(1): 8909, 2024 04 17.
Article in English | MEDLINE | ID: mdl-38632352

ABSTRACT

Among vertebrates, sharks exhibit both large and heterogeneous genome sizes ranging from 2.86 to 17.05 pg. Aiming for a better understanding of the patterns and causalities of shark genome size evolution, we applied phylogenetic comparative methods to published genome-size estimates for 71 species representing the main phylogenetic lineages, life-histories and ecological traits. The sixfold range of genome size variation was strongly traceable throughout the phylogeny, with a major expansion preceding shark diversification during the late Paleozoic and an ancestral state (6.33 pg) close to the present-day average (6.72 pg). Subsequent deviations from this average occurred at higher rates in squalomorph than in galeomorph sharks and were unconnected to evolutionary changes in the karyotype architecture, which were dominated by descending disploidy events. Genome size was positively correlated with cell and nucleus sizes and negatively with metabolic rate. The metabolic constraints on increasing genome size also manifested at higher phenotypic scales, with large genomes associated with slow lifestyles and purely marine waters. Moreover, large genome sizes were also linked to non-placental reproductive modes, which may entail metabolically less demanding embryological developments. Contrary to ray-finned fishes, large genome size was associated neither with the taxonomic diversity of affected clades nor with low genetic diversity.


Subject(s)
Sharks , Animals , Phylogeny , Genome Size , Sharks/genetics , Vertebrates/genetics , Fishes/genetics , Evolution, Molecular
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