Adaptive radiation plays a fundamental role in our understanding of the evolutionary process. However, the concept has provoked strong and differing opinions concerning its definition and nature among researchers studying a wide diversity of systems. Here, we take a broad view of what constitutes an adaptive radiation, and seek to find commonalities among disparate examples, ranging from plants to invertebrate and vertebrate animals, and remote islands to lakes and continents, to better understand processes shared across adaptive radiations. We surveyed many groups to evaluate factors considered important in a large variety of species radiations. In each of these studies, ecological opportunity of some form is identified as a prerequisite for adaptive radiation. However, evolvability, which can be enhanced by hybridization between distantly related species, may play a role in seeding entire radiations. Within radiations, the processes that lead to speciation depend largely on (1) whether the primary drivers of ecological shifts are (a) external to the membership of the radiation itself (mostly divergent or disruptive ecological selection) or (b) due to competition within the radiation membership (interactions among members) subsequent to reproductive isolation in similar environments, and (2) the extent and timing of admixture. These differences translate into different patterns of species accumulation and subsequent patterns of diversity across an adaptive radiation. Adaptive radiations occur in an extraordinary diversity of different ways, and continue to provide rich data for a better understanding of the diversification of life.
The bithorax complex (BX-C) of Drosophila, one of two complexes that act as master regulators of the body plan of the fly, is included within a sequence of 338,234 bp (SEQ89E). This paper presents the strategy used in sequencing SEQ89E and an analysis of its open reading frames. The BX-C sequence (BXCALL) contains 314,895 bp obtained by deletion of putative genes that are located at each end of SEQ89E and appear to be functionally unrelated to the BX-C. Only 1.4% of BXCALL codes for the three homeodomaincontaining proteins of the complex. Principal findings include a putative ABD-A protein (ABD-AII) larger than a previously known ABD-A protein and a putative glucose transporter-like gene (1521 bp) located at or near the bithoraxoid (bxd), infra-abdominal-2 (iab-2) boundary on the opposite strand relative to that of the homeobox-containing genes.
With the human genome project advancing into what will be a 7-to 10-year DNA sequencing phase, we are presented with the challenge of developing strategies to convert genomic sequence data, as they become available, into biologically meaningful information. We have analyzed 680 kb of noncontiguous DNA sequence from a 1-Mb region of human chromosome 5q31, coupling computational analysis with gene expression studies of tissues isolated from humans as well as from mice containing human YAC transgenes. This genomic interval has been noted previously for containing the cytokine gene cluster and a quantitative trait locus associated with inflammatory diseases. Our analysis identified and verified expression of 16 new genes, as well as 7 previously known genes. Of the total of 23 genes in this region, 78% had similarity matches to sequences in protein databases and 83% had exact expressed sequence tag (EST) database matches. Comparative mapping studies of eight of the new human genes discovered in the 5q31 region revealed that all are located in the syntenic region of mouse chromosome 11q. Our analysis demonstrates an approach for examining human sequence as it is made available from large sequencing programs and has resulted in the discovery of several biomedically important genes, including a cyclin, a transcription factor that is homologous to an oncogene, a protein involved in DNA repair, and several new members of a family of transporter proteins.[The sequence data described in this paper are available via the internet at http://www-hgc.lbl.gov/sequencearchive.html.]The Genome Project has shifted only recently to the sequencing phase for humans (Marshall and Pennisi 1996) while significant progress has already been made on the sequencing of selected model organisms. The genomic sequence of several organisms, including two eubacteria Fraser et al. 1995), an archaeon (Bult et al. 1996), and the extensively studied eukaryote, Saccharomyces cerevisiae (Walsh and Barrell 1996), have already been completed. The strategy employed to computationally identify and analyze putative genes in these model organisms has consisted of identifying protein-coding open reading frames (ORFs) followed by a search of the databases to determine whether these ORFs are homologs of previously characterized genes. Surprisingly, almost one-half of the protein-coding ORFs revealed during the analyses of these model organism genomes have shown no homology to previously characterized genes (Dujon 1996). In contrast to the genomes of model organisms, in which contiguous and annotated sequence data were released at defined intervals, human genomic sequence is being released to the public domain in noncontiguous minimally annotated fragments. Because the human genome is significantly larger and more complex, it is clear that the approaches employed to analyze it will have to vary from the approaches used previously for the genomes of model organisms.The annotation of human genomic sequence is facilitated greatly by the availability of the large pub...
A new protocol for the selected omission of transsyndesmotic fixation in Weber class C ankle fractures was prospectively evaluated in 21 consecutive patients. As proposed in a previous cadaveric study (J. Bone Joint Surg., 71A:1548-1555, 1989), the protocol suggested that transsyndesmotic fixation was not required if (1) rigid bimalleolar fracture fixation was achieved or (2) lateral without medial fixation was obtained (i.e., with accompanying deltoid tears) if the fibular fracture was within 4.5 cm of the joint. According to this protocol, only 3 of 21 patients (14%) required transsyndesmotic fixation. Ten of the patients who did not receive transsyndesmotic fixation underwent pronation-external rotation stress radiographs in a fashion analogous to the previous cadaveric study. At 1- to 3-year follow-up, no stress (N = 10) or static view (N = 18) widening of the mortise or syndesmosis was seen in any patient, which supports (with the above guidelines) a limited, rather than routine, use of supplemental transsyndesmotic fixation. Clinical results from this prospective study seem to substantiate previously proposed biomechanical guidelines for the selected omission of transsyndesmotic fixation. Given these guidelines, transsyndesmotic fixation was unnecessary in many cases and the need can be determined before surgery by assessing the integrity of the deltoid ligament and level of the fibular fracture.
Many species in high-diversity assemblages appear to coexist in similar ecological niches. It has been proposed that interspecific resource partitioning in these assemblages may only occur during periods of resource scarcity. We tested this hypothesis by measuring resource abundance, dietary overlap, foraging rate, and territoriality in a Lake Malawi rock cichlid assemblage over a period of 1 year. Our study examined two pairs of morphologically similar species, with each pair comprising one native species and one invader species that has successfully established after being translocated from another region of the lake. All four species changed their diet and foraging rate in response to seasonal variation in resource abundance. However, dietary overlap within both species pairs remained high in all seasons and was not influenced by resource availability. Similarly, territoriality did not decline during periods of low resource availability, suggesting no decrease in the strength of interspecific competition. These data suggest that these species pairs are successfully coexisting despite substantial niche overlap during resource scarcity. Thus, the coexistence of species within this radiation may not depend on the evolution of divergent resource use patterns.
A PCR-based sequence-tagged site (STS) content mapping strategy has been used to generate a physical map with 90% coverage of the 120-Mb euchromatic portion of the Drosophila genome. To facilitate map completion, the bulk of the STS markers was chosen in a nonrandom fashion. To ensure that all contigs were localized in relation to each other and the genome, these contig-building procedures were performed in conjunction with a large-scale in situ hybridization analysis of randomly selected clones from a Drosophila genomic library that had been generated in a PI cloning vector. To date, the map consists of 649 contigs with an STS localized on average every 50 kb. This is the first whole genome that has been mapped based on a library constructed with large inserts in a vector that is maintained in Escherichia coli as a single-copy plasmid.
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