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91.
Phylogenetic relationships within the Alcidae (Charadriiformes: Aves) inferred from total molecular evidence 总被引:4,自引:1,他引:3
The Alcidae is a unique assemblage of Northern Hemisphere seabirds that
forage by "flying" underwater. Despite obvious affinities among the
species, their evolutionary relationships are unclear. We analyzed
nucleotide sequences of 1,045 base pairs of the mitochondrial cytochrome b
gene and allelic profiles for 37 allozyme loci in all 22 extant species.
Trees were constructed on independent and combined data sets using maximum
parsimony and distance methods that correct for superimposed changes.
Alternative methods of analysis produced only minor differences in
relationships that were supported strongly by bootstrapping or standard
error tests. Combining sequence and allozyme data into a single analysis
provided the greatest number of relationships receiving strong support.
Addition of published morphological and ecological data did not improve
support for any additional relationship. All analyses grouped species into
six distinct lineages: (1) the dovekie (Alle alle) and auks, (2)
guillemots, (3) brachyramphine murrelets, (4) synthliboramphine murrelets,
(5) true auklets, and (6) the rhinoceros auklet (Cerorhinca monocerata) and
puffins. The two murres (genus Uria) were sister taxa, and the black
guillemot (Cepphus grylle) was basal to the other guillemots. The Asian
subspecies of the marbled murrelet (Brachyramphus marmoratus perdix) was
the most divergent brachyramphine murrelet, and two distinct lineages
occurred within the synthliboramphine murrelets. Cassin's auklet
(Ptychoramphus aleuticus) and the rhinoceros auklet were basal to the other
auklets and puffins, respectively, and the Atlantic (Fratercula arctica)
and horned (Fratercula corniculata) puffins were sister taxa. Several
relationships among tribes, among the dovekie and auks, and among the
auklets could not be resolved but resembled "star" phylogenies indicative
of adaptive radiations at different depths within the trees.
相似文献
92.
93.
Time of Recombination in the DROSOPHILA MELANOGASTER Oocyte. III. Selection and Characterization of Temperature-Sensitive and -Insensitive, Recombination-Deficient Alleles in Drosophila
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Grell RF 《Genetics》1984,108(2):425-443
The procedure for the selection of a temperature-sensitive recombination mutant in Drosophila is described. Use of this procedure has led to the recovery of three alleles at a new recombination locus called rec-1, located within the region of chromosome 3 circumscribed by Deficiency (3R)sbd105. One allele, rec-126, is temperature sensitive, and the other two alleles, rec-16 and rec-116, are temperature insensitive. Gene dosage studies reveal rec-126 to be a leaky mutant with greater recombination activity in two doses than in one. The other two alleles show no dose response, implying that they may be null mutants. The temperature response curves of rec-126 as a homozygote and in heteroallelic combination with rec-116 suggest that the sharp decrease in recombination between 28° and 31° indicates temperature denaturation of an enzyme or other protein specified by the mutant and associated with the recombination process. The ability of small changes in temperature to reverse or abolish polarity in recombination along the X chromosome arm in rec-1 26/rec-116 females brings into question the use of the "polarity" criterion to partition mutants into two functional types, i.e., precondition mutants that display polarity and exchange mutants that do not. Evidence that rec-1 may be part of a complex locus residing in a chromosome segment harboring a variety of recombination-related genes is presented. 相似文献
94.
Katherine N Choe Claudia M Nicolae Daniel Constantin Yuka Imamura Kawasawa Maria Rocio Delgado‐Diaz Subhajyoti De Raimundo Freire Veronique AJ Smits George‐Lucian Moldovan 《EMBO reports》2016,17(6):874-886
Defects in DNA replication, DNA damage response, and DNA repair compromise genomic stability and promote cancer development. In particular, unrepaired DNA lesions can arrest the progression of the DNA replication machinery during S‐phase, causing replication stress, mutations, and DNA breaks. HUWE1 is a HECT‐type ubiquitin ligase that targets proteins involved in cell fate, survival, and differentiation. Here, we report that HUWE1 is essential for genomic stability, by promoting replication of damaged DNA. We show that HUWE1‐knockout cells are unable to mitigate replication stress, resulting in replication defects and DNA breakage. Importantly, we find that this novel role of HUWE1 requires its interaction with the replication factor PCNA, a master regulator of replication fork restart, at stalled replication forks. Finally, we provide evidence that HUWE1 mono‐ubiquitinates H2AX to promote signaling at stalled forks. Altogether, our work identifies HUWE1 as a novel regulator of the replication stress response. 相似文献
95.
Heat-Induced Exchange in the Fourth Chromosome of Diploid Females of Drosophila Melanogaster 总被引:2,自引:0,他引:2
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Rhoda F. Grell 《Genetics》1971,69(4):523-527
96.
97.
The chemical relaxation times of two different two-step equilibrium reactions, characterized by a 1:1 binding process followed by a subsequent rearrangement step and a stepwise 1:2 binding reaction, are analyzed for the purpose of qualitative model discrimination and quantitative determination of kinetic parameters. The equations describing the dependences of the two reciprocal relaxation times on suitable concentrations are given for both models in the general case as well as for four different limiting situations which are characterized by well separated relaxation times. The conditions corresponding to the limiting cases are expressed in terms of strong, weak and no coupling between the two partial equilibrium steps involved in both models. The coupling strength depends on the rate constants as well as on the total concentrations of the reactants. Criteria to discriminate between these two reaction models under defined limiting conditions are developed. In the general case, the product of both reciprocal relaxation times can be used to distinguish both models. If only one relaxation time can be resolved experimentally, it is possible under conditions described to determine only a reduced set of individual rate constants for most of the limiting cases considered. If both relaxation times are observed, all rate constants are determinable in the general case as well as in most of the limiting cases discussed. 相似文献
98.
Jurriaan J Hölzenspies Willem Stoorvogel Ben Colenbrander Bernard AJ Roelen Dagmar R Gutknecht Theo van Haeften 《BMC developmental biology》2009,9(1):1-16
Background
Fibronectin 1 (FN1), a glycoprotein component of the extracellular matrix, exerts different functions during reproductive processes such as fertilisation, gastrulation and implantation. FN1 expression has been described to increase significantly from the morula towards the early blastocyst stage, suggesting that FN1 may also be involved in early blastocyst formation. By alternative splicing at 3 defined regions, different FN1 isoforms are generated, each with a unique biological function. The analysis of the alternative FN1 splicing on the one hand and the search for candidate FN1 receptors on the other hand during early bovine embryo development may reveal more about its function during bovine preimplantation embryo development. 相似文献99.
Tania Maes Sharen Provoost Ellen A Lanckacker Didier D Cataldo Jeroen AJ Vanoirbeek Benoit Nemery Kurt G Tournoy Guy F Joos 《Respiratory research》2010,11(1):1-16
Background
Nicotinic acetylcholine receptors (nAChR) have been identified on a variety of cells of the immune system and are generally considered to trigger anti-inflammatory events. In the present study, we determine the nAChR inventory of rat alveolar macrophages (AM), and investigate the cellular events evoked by stimulation with nicotine.Methods
Rat AM were isolated freshly by bronchoalveolar lavage. The expression of nAChR subunits was analyzed by RT-PCR, immunohistochemistry, and Western blotting. To evaluate function of nAChR subunits, electrophysiological recordings and measurements of intracellular calcium concentration ([Ca2+]i) were conducted.Results
Positive RT-PCR results were obtained for nAChR subunits α3, α5, α9, α10, β1, and β2, with most stable expression being noted for subunits α9, α10, β1, and β2. Notably, mRNA coding for subunit α7 which is proposed to convey the nicotinic anti-inflammatory response of macrophages from other sources than the lung was not detected. RT-PCR data were supported by immunohistochemistry on AM isolated by lavage, as well as in lung tissue sections and by Western blotting. Neither whole-cell patch clamp recordings nor measurements of [Ca2+]i revealed changes in membrane current in response to ACh and in [Ca2+]i in response to nicotine, respectively. However, nicotine (100 μM), given 2 min prior to ATP, significantly reduced the ATP-induced rise in [Ca2+]i by 30%. This effect was blocked by α-bungarotoxin and did not depend on the presence of extracellular calcium.Conclusions
Rat AM are equipped with modulatory nAChR with properties distinct from ionotropic nAChR mediating synaptic transmission in the nervous system. Their stimulation with nicotine dampens ATP-induced Ca2+-release from intracellular stores. Thus, the present study identifies the first acute receptor-mediated nicotinic effect on AM with anti-inflammatory potential. 相似文献100.
Andreas Stein Martina Knödler Markus Makowski Sandra Kühnel Stefan Nekolla Alexandra Keithahn Eliane Weidl Philip Groha Maren Schürmann Atti Saraste Rene Botnar Robert AJ Oostendorp Ilka Ott 《BMC cardiovascular disorders》2010,10(1):43