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Extreme environmental change and evolution: stress-induced morphological variation is strongly concordant with patterns of evolutionary divergence in shrew mandibles.

Morphological structures often consist of simpler traits which can be viewed as either integrated (e.g. correlated due to functional interdependency) or non-integrated (e.g. functionally independent) traits. The combination of a long-term stabilizing selection on the entire structure with a short-term directional selection on an adaptively important subset of traits should result in long historical persistence of integrated functional complexes, with environmentally induced variation and macroevolutionary change confined mostly to non-integrated traits. We experimentally subjected populations of three closely related species of Sorex shrews to environmental stress. As predicted, we found that most of the variation in shrew mandibular shape was localized between rather than within the functional complexes; the patterns of integration did not change between the species. The stress-induced variation was confined to nonintegrated traits and was highly concordant with the patterns of evolutionary change--species differed in the same set of non-integrated traits which were most sensitive to stress within each species. We suggest that low environmental and genetic canalization of non-integrated traits may have caused these traits to be most sensitive not only to the environmental but also to genetic perturbations associated with stress. The congruence of stress-induced and between-species patterns of variation in non-integrated traits suggests that stress-induced variation in these traits may play an important role in species divergence.

Animals↗

Functional and morphological stasis during molecular evolution.

The evolutionary distance between two sets of proteins was estimated using the techniques of Miyata and Yasunaga (1980) and Kimura (1980). Human beta 2-microglobulin was compared with the homologous murine molecule, while human and equine alpha-globin were similarly treated. It was found that a large amount of molecular evolution has occurred in beta 2-microglobulin since its divergence from the common ancestor of mice and humans. Kimura's estimate of evolutionary distance, K, is 0.353, while those of Miyata and Yasunaga are KS = 0.708 and KA = 0.171. The respective values for human and equine alpha-globin are 0.152, 0.293, and 0.084. In spite of this molecular evolution, it is shown that murine beta 2-microglobulin can effect the expression of HLA class I antigens on the surface of human-mouse hybrid cells and that the tertiary structures of human and equine deoxyhemoglobin are nearly identical. These observations are discussed in the light of Kimura's theory of neutral allelic drift.

Amino Acid Sequence↗

The evolution and distribution of morphological changes in the nervous system of the common marmoset following the acute administration of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine.

Six young adult marmosets received 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine in multiple doses (total 8-16 mg/kg over 2-13 days) sufficient to produce a parkinsonian syndrome and were killed up to 3.5 months later. Cellular changes were found in the substantia nigra, ventral tegmental area, and hypothalamus. The earliest histological abnormalities were axonal swellings in proximal parts of nigrostriatal axons. Subsequent changes in the substantia nigra were reduced Nissl staining, reduced cell volume, and aggregation and loss of melanin granules. Other effects were reduced nuclear and nucleolar volumes, depletion of cells, and hyperplasia of glial cells. Shrunken cytoplasm and nuclei stained uniformly with eosin, and no cells showed cytoplasmic swellings or inclusions. These cellular alterations, with nuclear changes resembling karyolysis, do not occur in Parkinson's disease, which is characterised by Lewy body inclusions and signs of chromatolysis. The rapid appearance of axonal swellings, disruption of Nissl substance, and cell shrinkage suggest an insult to energy producing mechanisms. In this study, the absence of histological evidence of toxicity in the locus coeruleus and also in the substantia innominata and in serotonergic cell groups is unlike the more widespread degenerative changes of Parkinson's disease.

1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine↗

Patterns of morphological, biochemical, and molecular evolution in the Oeneis chryxus complex (Lepidoptera: Satyridae): a test of historical biogeographical hypotheses.

Surveys of allozyme allele frequency and mitochondrial DNA (mtDNA) sequence variation were employed to test historical biogeographical hypotheses on the origin and unique distribution of the synchronized biennial, high-altitude butterflies of the Oeneis chryxus complex in western North America. Populations of O. c. stanislaus and O. ivallda from the central and northern Sierra Nevada are indistinguishable by use of allozyme allele frequency data, possessed nearly identical mtDNA cytochrome oxidase subunit 1 (COI) haplotypes, and were found to be relatively distantly related to O. c. chryxus from the Snake Range in eastern Nevada. However, individuals of O. ivallda from Piute Pass in the southern Sierra Nevada are more variable, with some individuals sharing mtDNA characteristics with O. c. chryxus. We find little support for the hypothesis proposed by W. Hovanitz in 1940 that O. c. stanislaus invaded the central Sierra Nevada from across the Great Basin and displaced O. ivallda, but cannot reject the hypothesis that ancestral Oeneis dispersed across the Great Basin to California. This result is congruent with hypotheses of dispersal across the Great Basin for the origin of some Sierran alpine organisms.

Alleles↗

Aspects of the structure and development of monotreme spermatozoa and their relevance to the evolution of mammalian sperm morphology.

The elongated spermatid nuclei of monotremes exhibit a circumferentially arranged spiral pattern of chromatin condensation, and ultimately form helical filiform sperm heads up to 50 microns long and either circular or slightly oval in transverse section. The acrosome is formed by the collapse of the proacrosomal vacuole onto the rostral surface of the elongating nucleus. However, genesis of acrosomal material occurs in the absence of a prominent proacrosomal granule. The flagellum becomes inserted into the distal extremity of the nucleus, the most proximal mitochondria of the midpiece directly abutting the nuclear membrane, so that a prominent neck region is absent. The axoneme is simple and, in the midpiece, small dense peripheral fibres are closely applied to the outer surface of each of the nine microtubule doublets. The cortical fibrous sheath of the principal piece is an anastomosing spiral that lacks lateral columnar elements. The spermatozoal cytoplasmic droplet undergoes migration and is lost during epididymal passage. Monotreme spermatozoa exhibit a montage of features, some of these being also found in marsupials and some in sauropsidan vertebrates, as well as a number of their own distinctive features. It is concluded that monotreme spermatozoa also have a close affinity with the unspecialised spermatozoa of some eutherian mammals.

Animals↗

Experimental hepatic iron overload in the baboon: results of a two-year study. Evolution of biological and morphologic hepatic parameters of iron overload.

Four baboons receiving intramuscular iron for 15 months were compared with two control baboons. From the overall two-year observation period the following data emerge: (1) The baboon is a suitable animal for obtaining a massive and chronic iron overload. Liver iron concentrations reached very high levels (ranging from 41.3 to 180.6 mumol/100 mg dry weight vs 1.7 +/- 0.5, mean +/- SEM, in controls), and a major liver iron overload (ie, with concentration values greater than or equal to 18) was present in all four animals for an average period of 16.5 months (range 14-19). (2) When compared with human hepatic iron-overload disorders, iron distribution was similar to that observed in secondary (transfusional) hepatic siderosis since iron deposits were found primarily in sinusoidal cells. However, a marked parenchymal siderosis was also obtained close to that observed in primary (genetic) siderosis. Iron toxicity was present biologically as indicated by an increase in serum transaminases. Histologically, a slight fibrosis was observed in the most heavily iron-overloaded baboon. On the whole, this study of subhuman primates brings new evidence that iron per se has only a minor hepatic damaging effect. It also suggests that the iron-overloaded baboon liver provides a promising tool for the study of liver cell disturbances in human iron overload.

Animals↗

Equine cutaneous mastocytoma: morphology, biological behaviour and evolution of the lesion.

Thirty equine cutaneous mastocytomas were examined histologically and two were studied ultrastructurally. Lesions were characterized by distinct sheets of well-differentiated mast cells with variable degrees of eosinophil infiltration, collagen degeneration, necrosis, granulomatous inflammation and fibrosis. Twenty-two of 25 growths did not recur for up to 6 years after surgical excision, two recurred at the surgical site and one spontaneously regressed less than 3 months after obtaining a biopsy sample. Equine cutaneous mastocytoma is a benign proliferative lesion which seldom recurs after excision. The varied histological presentation of equine mastocytoma can be attributed to a sequence of events initiated by a cutaneous mast cell proliferation. It is suggested that these mast cells release chemotactic factors for eosinophils which accumulate and degranulate, initiating collagen degeneration and cellular necrosis with subsequent granulomatous inflammation and fibrosis. The focal spontaneous nature of the primary mast cell proliferation is typical of neoplasia.

Animals↗

The teeth of the horse: evolution and anatomo-morphological and radiographic study of their development in the foetus.

The aim of this work was to study the ontogenetic process in teeth from their early appearance in the ossifying matrix of the mandible and maxilla, in different foetuses of scalar ages. Radiographic examinations of the skull and mandible hemisections were performed and the latero-medial (LM) and dorsoventral (DV) projections for the skull and mandible were analysed. A high-definition film-screen combination was used for this study. The exposure values ranged from 35 kV/6 mAs to 58 kV/10 mAs, according to the size of the skulls and their degree of ossification. The first dental germ observed was the P3, at 138-140 days of pregnancy. At 146 days, P2 and P4 dental germs were visible. At 160-168 days, the dental germ of the first deciduous incisor tooth (I1) appeared; at 180-188 days of pregnancy the germ of the second (I2), and at 224 days the germ of the third (I3), were detectable. At 275 days the dental germ of the mandibular first molar tooth (M1) appeared, while the maxillary M1, which was not visible radiographically, was represented by a jelly-like amorphous body within its alveolar cavity.

Aging↗

Maternal effects and the evolution of behavioral and morphological characters: a literature review indicates the importance of extended maternal care.

Using literature data on reciprocal crosses, I estimated the influence of maternal effects on morphological and behavioral traits and compared these effects between mammals, birds, insects with homogametic females, and butterflies. In birds and in both groups of insects, no detectable difference between the reciprocal hybrids was observed on average, showing that in these groups, the contribution of maternal effects to the difference between the parental lines is at least rather small. In contrast to the other groups, mammals showed a significant and large influence of maternal effects on the examined characters. The large maternal effects in mammals are probably due to the extended period of parental care during gestation and lactation. It is concluded that maternal effects contributing to differences between parental lines are only widespread and important in mammals. It should be noted that these results do not show that maternal effects are absent in other animals. In the three examined groups, maternal effects may only evolve much more slowly than traits influenced by nuclear genes.

Animals↗

Morphological variability and degenerative evolution of human hepatic hydatid cysts.

The findings are presented of a macro and microscopic investigation of 89 hydatid hepatic cysts removed intact from 59 patients by total pericystectomy. Detailed analysis revealed significant morphostructural variability and cysts grouped into 10 types were characterized, providing useful clinical indications. Only 30 cysts resulted fertile (33.7%), probably due to mean age of sample; 7 of these were "classic" cysts, 1 "septated" and 22 "multivesicular" packed with daughter cysts (DC), of varying turgidity or collapsed. Among the remaining 59 sterile cysts, 52 were degenerated and classified as "hyperlaminated" cysts due to the presence of large convoluted sheets of laminar tissue (SLT) surrounded by varying amounts of caseous (40 specimens), granular (6) or gelatinous (6) matrix. Moreover, "multivesicular", "acephalocyst", "caseous" and "serous" cysts were also recovered among the sterile specimens. Some "multivesicular" cysts (14) appeared as "transitional forms" towards the various types of "hyperlaminated" cysts containing all different forms of DC and large SLT intermingled with a variously degenerated matrix. The comprehensive study allows to hypothesize the train of events leading, over the years, to the gradual transformation and degeneration of the larval form Echinococcus granulosus in the human liver.

Adolescent↗

[Cloning and analysis of rat heat shock factor binding protein 1 cDNA].

Heat shock factor binding protein 1(HSBP1) is a nuclear-localized, novel, conserved, low molecular weight (< 100 residues) transcriptional factor, which may repress the activity of the heat shock factor 1 (HSF1) by binding HSF1 active trimerization domain. HSBP1 gene have been cloned in human and mouse, but not reported in rat. In this paper, a pair of consensus degenerate primers were designed based on N-terminal and C-terminal conservative amino acid sequence. Using RT-PCR method, hsbp1 gene fragment was amplified and cloned from total RNA extracted from rat C6 glioma cells. Then the EST was probed to isolate the rat full-length hsbp1 cDNA by in situ hybridization from a rat C6 glioma cells cDNA library. The full-length hsbp1 was deposited in GenBank (accession No. AY522937). It was blasted in RGD (rat genome database) and was localized in 19q12 and composed of four extrons and three introns. The distance between the first extron and the fourth extron was 5829bp. Then its Uinigene was searched, results showed HSBP1 existed widely in all kinds of organs and tissues, the data suggested that it may play a important roles in physiological activity. In addition, the sequence similarity and phylogenetic relationship were compared with DNAman tool. The result showed the relationship is consistent between the similarity of amino acid sequence and phylogenetic evolution from morphological of those species which were nearly in evolution.

Amino Acid Sequence↗

[Morphologic characteristics of the evolution of myocardial infarct after effective thrombolytic therapy].

Stroma and vessels which remain in the zone of myocardial infarction (MI) after thrombolytic therapy has restored impaired circulation during early hours of MI onset may produce foci of necrosis responsible for accelerated MI formation both in the periphery and centre of the foci. Hemorrhagic MI development can be related to microvascular and intramural vein spasms at early stages of the blood supply recovery. Fibrinoid necrosis of the wall and thrombosis of the lumen were observed in relevant vessels later on. These were associated with disturbed blood outflow from the infarction zone and hemorrhagic saturation of the interstice and cardiomyocytes.

Aged↗