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      Chance and necessity: the evolution of morphological complexity and diversity.

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      Springer Nature

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          Abstract

          The primary foundation for contemplating the possible forms of life elsewhere in the Universe is the evolutionary trends that have marked life on Earth. For its first three billion years, life on Earth was a world of microscopic forms, rarely achieving a size greater than a millimetre or a complexity beyond two or three cell types. But in the past 600 million years, the evolution of much larger and more complex organisms has transformed the biosphere. Despite their disparate forms and physiologies, the evolution and diversification of plants, animals, fungi and other macroforms has followed similar global trends. One of the most important features underlying evolutionary increases in animal and plant size, complexity and diversity has been their modular construction from reiterated parts. Although simple filamentous and spherical forms may evolve wherever cellular life exists, the evolution of motile, modular mega-organisms might not be a universal pattern.

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          Most cited references56

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          A gene complex controlling segmentation in Drosophila.

          E B Lewis (1978)
          The bithorax gene complex in Drosophila contains a minimum of eight genes that seem to code for substances controlling levels of thoracic and abdominal development. The state of repression of at least four of these genes is controlled by cis-regulatory elements and a separate locus (Polycomb) seems to code for a repressor of the complex. The wild-type and mutant segmentation patterns are consistent with an antero-posterior gradient in repressor concentration along the embryo and a proximo-distal gradient along the chromosome in the affinities for repressor of each gene's cis-regulatory element.
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            The genome sequence of the food-borne pathogen Campylobacter jejuni reveals hypervariable sequences.

            Campylobacter jejuni, from the delta-epsilon group of proteobacteria, is a microaerophilic, Gram-negative, flagellate, spiral bacterium-properties it shares with the related gastric pathogen Helicobacter pylori. It is the leading cause of bacterial food-borne diarrhoeal disease throughout the world. In addition, infection with C. jejuni is the most frequent antecedent to a form of neuromuscular paralysis known as Guillain-Barré syndrome. Here we report the genome sequence of C. jejuni NCTC11168. C. jejuni has a circular chromosome of 1,641,481 base pairs (30.6% G+C) which is predicted to encode 1,654 proteins and 54 stable RNA species. The genome is unusual in that there are virtually no insertion sequences or phage-associated sequences and very few repeat sequences. One of the most striking findings in the genome was the presence of hypervariable sequences. These short homopolymeric runs of nucleotides were commonly found in genes encoding the biosynthesis or modification of surface structures, or in closely linked genes of unknown function. The apparently high rate of variation of these homopolymeric tracts may be important in the survival strategy of C. jejuni.
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              Comparative genomics of the eukaryotes.

              A comparative analysis of the genomes of Drosophila melanogaster, Caenorhabditis elegans, and Saccharomyces cerevisiae-and the proteins they are predicted to encode-was undertaken in the context of cellular, developmental, and evolutionary processes. The nonredundant protein sets of flies and worms are similar in size and are only twice that of yeast, but different gene families are expanded in each genome, and the multidomain proteins and signaling pathways of the fly and worm are far more complex than those of yeast. The fly has orthologs to 177 of the 289 human disease genes examined and provides the foundation for rapid analysis of some of the basic processes involved in human disease.
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                Author and article information

                Journal
                Nature
                Nature
                Springer Nature
                0028-0836
                0028-0836
                Feb 22 2001
                : 409
                : 6823
                Affiliations
                [1 ] Howard Hughes Medical Institute and Laboratory of Molecular Biology, University of Wisconsin-Madison, 53706-1596, USA. sbcarrol@facstaff.wisc.edu
                Article
                10.1038/35059227
                11234024
                00fef410-8bcd-4613-b84e-3c5d8e34455e
                History

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