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Positive selection is a general phenomenon in the evolution of abalone sperm lysin 总被引:36,自引:21,他引:15
Lysin is a 16kDa acrosomal protein used by abalone sperm to create a hole
in the egg vitelline envelope (VE). The interaction of lysin with the VE is
species-selective and is one step in the multistep fertilization process
that restricts heterospecific (cross-species) fertilization. For this
reason, the evolution of lysin could play a role in establishing prezygotic
reproductive isolation between species. Previously, we sequenced sperm
lysin cDNAs from seven California abalone species and showed that positive
Darwinian selection promotes their divergence. In this paper an additional
13 lysin sequences are presented representing species from Japan, Taiwan,
Australia, New Zealand, South Africa, and Europe. The total of 20 sequences
represents the most extensive analysis of a fertilization protein to date.
The phylogenetic analysis divides the sequences into two major clades, one
composed of species from the northern Pacific (California and Japan) and
the other composed of species from other parts of the world. Analysis of
nucleotide substitution demonstrates that positive selection is a general
process in the evolution of this fertilization protein. Analysis of
nucleotide and codon usage bias shows that neither parameter can account
for the robust data supporting positive selection. The selection pressure
responsible for the positive selection on lysin remains unknown.
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2.
Maize streak virus genes essential for systemic spread and symptom development 总被引:22,自引:0,他引:22
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The entire genome of single component geminiviruses such as maize streak virus (MSV) consists of a single-stranded circular DNA of ~2.7 kb. Although this size is sufficient to encode only three average sized proteins, the virus is capable of causing severe disease of many monocots with symptoms of chlorosis and stunting. We have identified viral gene functions essential for systemic spread and symptom development during MSV infection. Deletions and gene replacement mutants were created by site-directed mutagenesis and insertion between flanking MSV or reporter gene sequences contained in Agrobacterium T-DNA derived vectors. Following Agrobacterium-mediated inoculation of maize seedlings, the mutated MSV DNAs were excised from these binary vectors by homologous recombination within the flanking sequences. Our analyses show that the capsid gene of MSV, while not required for replication, is essential for systemic spread and subsequent disease development. The `+' strand open reading frame (ORF) located immediately upstream from the capsid ORF and predicted to encode a 10.9 kd protein was also found to be dispensable for replication but essential for systemic spread. By this analysis, MSV sequences that support autonomous replication were localized to a 1.7 kb segment containing the two viral intergenic regions and two overlapping complementary `-' strand ORFs. Despite the inability of the gene replacement mutants to spread systemically, both inoculated and newly developed leaves displayed chlorotic patterns similar to the phenotype observed in certain developmental mutants of maize. The similarity of the MSV mutant phenotype to these developmental mutants is discussed. 相似文献
3.
Mitochondrial DNA and bindin gene sequence evolution among allopatric species of the sea urchin genus Arbacia 总被引:3,自引:1,他引:2
Sea urchins of the genus Arbacia (order Stirodonta) have discontinuous
allopatric distributions ranging over thousands of kilometers.
Mitochondrial DNA (mtDNA) sequences were used to reconstruct phylogenetic
relationships of four Arbacia species and their geographic populations.
There is little evidence of genetic structuring of populations within
species, except in two cases at range extremes. The mtDNA sequence
differentiation between species suggests that divergence occurred about 4-9
MYA. Gene sequences encoding the sperm protein bindin and its intron were
obtained and compared with the mtDNA phylogeny. Sea urchins among the
well-studied echinoid order Camarodonta, with degrees of mtDNA divergence
similar to those of Arbacia species, are known to have remarkable variation
in bindin. However, in Arbacia, little variation in deduced amino acid
sequences of bindin was found, indicating that purifying selection acts on
the protein. In contrast, bindin intron sequences showed much
differentiation, including numerous insertion/deletions. Fertilization
experiments performed between a divergent pair of Arbacia species from the
Atlantic and Pacific Oceans revealed no evidence of blocks to gamete
recognition. In Arbacia, fertilization specificities may have evolved
relatively slowly as a result of extensive gene flow within species,
greater functional constraint on the bindin polypeptide, or reduced
selective pressure for species recognition in singly occurring species.
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4.
Females of the sea urchin Strongylocentrotus purpuratus differ in the structures of their egg jelly sulfated fucans 总被引:1,自引:0,他引:1
The egg jelly coats of sea urchins contain sulfated fucans which bind to a
sperm surface receptor glycoprotein to initiate the signal transduction
events resulting in the sperm acrosome reaction. The acrosome reaction is
an ion channel regulated exocytosis which is an obligatory event for sperm
binding to, and fusion with, the egg. Approximately 90% of individual
females of the sea urchin Strongylocentrotus purpuratus spawned eggs having
only one of two possible sulfated fucan electrophoretic isotypes, a slow
migrating (sulfated fucan I), or a fast migrating (sulfated fucan II)
isotype. The remaining 10% of females spawned eggs having both sulfated
fucan isotypes. The two sulfated fucan isotypes were purified from egg
jelly coats and their structures determined by NMR spectroscopy and
methylation analysis. Both sulfated fucans are linear polysaccharides
composed of 1-->3-linked alpha-L-fucopyranosyl units. Sulfated fucan I
is entirely sulfated at the O -2 position but with a heterogeneous
sulfation pattern at O -4 position. Sulfated fucan II is composed of a
regular repeating sequence of 3 residues, as follows: [3-alpha-L-Fuc p -
2,4(OSO3)-1-->3-alpha-L-Fuc p -4(OSO3)-1-->3-alpha-L-Fuc p -4(OSO3)-
1]n. Both purified sulfated fucans have approximately equal potency in
inducing the sperm acrosome reaction. The significance of two structurally
different sulfated fucans in the egg jelly coat of this species could
relate to the finding that the sperm receptor protein which binds sulfated
fucan contains two carbohydrate recognition modules of the C-type lectin
variety which differ by 50% in their primary structure.
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5.
D. A. Lalli A. G. Abbott T. N. Zhebentyayeva M. L. Badenes V. Damsteegt J. Polák B. Krška J. Salava 《Tree Genetics & Genomes》2008,4(3):481-493
Plum pox virus (sharka; PPV) can cause severe crop loss in economically important Prunus species such as peach, plum, apricot, and cherry. Of these species, certain apricot cultivars (‘Stark Early Orange’, ‘Goldrich’,
‘Harlayne’) display significant levels of resistance to the disease and are the genetic substrate for studies of several xlaboratories
working cooperatively to genetically characterize and mark the resistance locus or loci for marker-assisted breeding. The
goals of the work presented in this communication are the characterization of the genetics of PPV resistance in ‘Stark Early
Orange’ and the development of co-dominant molecular markers for marker-assisted selection (MAS) in PPV resistance breeding.
We present the first genetic linkage map for an apricot backcross population of ‘Stark Early Orange’ and the susceptible cultivar
‘Vestar’ that segregates for resistance to PPV. This map is comprised of 357 loci (330 amplified fragment length polymorphisms
(AFLPs), 26 simple sequence repeats (SSRs), and 1 morphological marker for PPV resistance) assigned to eight linkage groups.
Twenty-two of the mapped SSRs are shared in common with genetic reference map for Prunus (T × E; Joobeur et al. 1998) and anchor our apricot map to the general Prunus map. A PPV resistance locus was mapped in linkage group 1 and four AFLP markers segregating with the PPV resistance trait,
identified through bulk segregant analysis, facilitated the development of SSRs in this region.
Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.
Lalli, D.A. and Salava, J. contributed equally to this work. 相似文献
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F. E. Gildow V. D. Damsteegt A. L. Stone O. P. Smith S. M. Gray 《Journal of Phytopathology》2000,148(6):333-342
Transmission of soybean dwarf viruses (SbDV) indigenous to Japan (SbDV‐D) and to the eastern United States (SbDV‐Va19) were compared in vector and nonvector aphid species. Absolute vector‐specificity was maintained when Aulacorthum solani, Acyrthosiphon pisum, and Myzus persicae were allowed to feed on solutions of either virus (100 μg/ml) through Parafil© membranes. SbDVD was transmitted only by A. solani, and SbDV‐Va19 was transmitted only by A. pisum and M. persicae. Similar results were obtained when individual aphids were micro‐injected with 2 ng virus and subsequently allowed to feed on healthy plants. Ultrastructural studies of A. solani and M. persicae indicated that both SbDV‐D and SbDV‐Va20 were acquired specifically through the aphid hindgut. No difference in hindgut acquisition specificity was observed, and both A. solani and M. persicae were able to transport SbDV‐D and SbDV‐Va20 into the haemocoel by endocytotic/exocytotic pathways. When injected, SbDV was shown to be associated with only the accessory salivary glands (ASG) in aphids, indicating a high level of tissue specificity. Two different interactions with the ASG were observed for SbDV‐D and SbDV‐Va20 in A. solani and M. persicae. SbDV‐D penetrated the ASG basal lamina of A. solani, but was never observed in the basal lamina of M. persicae. The ASG basal lamina was a barrier to SbDV‐D transmission by M. persicae. SbDV‐Va19 penetrated the ASG basal lamina of both A. solani and M. persicae. However, SbDV‐Va20 was not observed in the ASG cytoplasm in A. solani, indicating that the basal plasmalemma functioned as the transmission barrier. Observations indicated that capsid protein structure, aphid basal lamina composition and cell membrane components influenced virus‐aphid interactions regulating SbDV transmission. 相似文献
8.
Identification and mapping of resistance gene analogs (RGAs) in Prunus: a resistance map for Prunus 总被引:1,自引:0,他引:1
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