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1.
Transposable elements reveal the impact of introgression,rather than transposition,in Pisum diversity,evolution, and domestication 总被引:4,自引:0,他引:4
Vershinin AV Allnutt TR Knox MR Ambrose MJ Ellis TH 《Molecular biology and evolution》2003,20(12):2067-2075
The genetic structure and evolutionary history of the genus Pisum were studied exploiting our germplasm collection to compare the contribution of different mechanisms to the generation of diversity. We used sequence-specific amplification polymorphism (SSAP) markers to assess insertion site polymorphism generated by a representative of each of the two major groups of LTR-containing retrotransposons, PDR1 (Ty1/copia-like) and Cyclops (Ty3/gypsy-like), together with Pis1, a member of the En/Spm transposon superfamily. The analysis of extended sets of the four main Pisum species, P. fulvum, P. elatius, P. abyssinicum, and P. sativum, together with the reference set, revealed a distinct pattern of the NJ (Neighbor-Joining) tree for each basic lineage, which reflects the different evolutionary history of each species. The SSAP markers showed that Pisum is exceptionally polymorphic for an inbreeding species. The patterns of phylogenetic relationships deduced from different transposable elements were in general agreement. The retrotransposon-derived markers gave a clearer separation of the main lineages than the Pis1 markers and were able to distinguish the truly wild form of P. elatius from the antecedents of P. sativum. There were more species-specific and unique PDR1 markers than Pis1 markers in P. fulvum and P. elatius, pointing to PDR1 activity during speciation and diversification, but the proportion of these markers is low. The overall genetic diversity of Pisum and the extreme polymorphism in all species, except P. abyssinicum, indicate a high contribution of recombination between multiple ancestral lineages compared to transposition within lineages. The two independently domesticated pea species, P. abyssinicum and P. sativum, arose in contrasting ways from the common processes of hybridization, introgression, and selection without associated transpositional activity. 相似文献
2.
Recurrent recruitment of the THAP DNA-binding domain and molecular domestication of the P-transposable element 总被引:2,自引:0,他引:2
The recently described THAP domain motif characterizes a DNA-binding domain (DBD) that is widely conserved in human and in animals. It presents a similarity with the DBD of the P element transposase of D. melanogaster. We show here that the P Drosophila neogenes derived from P-transposable elements conserve the THAP domain. Moreover, secondary rearrangements by exon shuffling indicate the recurrent recruitment of this domain by the host genome. As P sequences and THAP genes are found together in many animal genomes, we discuss the possibility that the THAP proteins have acquired their domain as a result of recurrent molecular domestication of P-transposable elements. 相似文献
3.
Tetsuo Ohi‐Toma Sugong Wu Hiroko Murata Jin Murata 《Botanical journal of the Linnean Society. Linnean Society of London》2016,182(1):100-114
Arisaema has a long and complicated taxonomic history regarding its infrageneric classification. In the latest system, 14 sections were recognized, based on an unpublished, tentative phylogenetic analysis; in addition the type species and nomenclatural priority for each section were confirmed. Here, we present an updated, genus‐wide phylogenetic analysis, based on four plastid non‐coding regions (3′trnL–trnF, rpl20–5′rps12, psbB–psbH and rpoC2–rps2) for > 150 accessions. The maximum parsimony and maximum likelihood phylogenetic analyses identified eight major clades and one branch with unique sequence variation, although the relationships were unclear due to a polytomy and weak support. In the phylogenetic trees, most of the sections proposed in the latest system were distinct and corresponded to the major clades, but some sections are not monophyletic. On the basis of the phylogenetic relationship: (1) A. schimperianum is treated as a member of section Arisaema, rather than section Tenuipistillata or section Sinarisaema; and (2) section Fimbriata, which was synonymised into section Attenuata in the latest system but is morphologically distinct from the other species, is redefined as a monotypic section. In conclusion, we recognize 15 sections of Arisaema and species‐level classifications are discussed in a phylogenetic context. 相似文献
4.
Vadim V. Goremykin Sabine Hansmann William F. Martin 《Plant Systematics and Evolution》1997,206(1-4):337-351
Fifty-eight homologous protein sequences from the completely sequenced chloroplast genomes ofZea mays, Oryza sativa, Nicotiana tabacum, Pinus thunbergii, Marchantia polymorpha andPoryphyra purpurea were investigated. Analyzed individually, only 40 of the 58 proteins gave the true, known topology for these species. Trees constructed from the concatenated 14295 amino acid alignment and from automatically generated subsets of the data containing successively fewer polymorphisms were used to estimate theNicotiana-Zea andPinus-angiosperm divergence times as 160 and 348 million years, respectively, with an uncertainty of about 10%. These estimates based upon phylogenetic analysis of protein data from complete chloroplast genomes are in much better accordance with current interpretations of fossil evidence than previous molecular estimates.This paper is dedicated to emer. Univ.-Prof. DrFriedrich Ehrendorfer on the occasion of his 70th birthday. 相似文献
5.
N. V. Joshi 《Journal of genetics》1990,69(3):127-139
For a population made up of individuals capable of sexual as well as asexual modes of reproduction, conditions for the spread
of a transposable element are explored using a one-locus, two-haplotype model. The analysis is then extended to include the
possibility that the transposable element can modulate the probability of sexual reproduction, thus casting Hickey’s (1982,Genetics 101: 519–531) suggestion in a population genetics framework. The model explicitly includes the cost of sexual reproduction,
fitness disadvantage to the transposable element, probability of transposition, and the predisposition for sexual reproduction
in the presence and absence of the transposable element. The model predicts several kinds of outcome, including initial frequency
dependence and stable polymorphism. More importantly, it is seen that for a wide range of parameter values, the transposable
element can go to fixation. Therefore it is able to convert the population from a predominantly asexual to a predominantly
sexual mode of reproduction. Viewed in conjunction with recent results implicating short stretches of apparently non-coding
DNA in sex determination (McCoubreyet al. 1988,Science 242: 1146–1151), the model hints at the important role this mechanism could have played in the evolution of sexuality. 相似文献
6.
Terezie Mandkov Kaylynn Ashby Bo J. Price Michael D. Windham John G. Carman Martin A. Lysak 《植物分类学报:英文版》2021,59(1):83-92
Apomixis in crucifer (Brassicaceae) species is rare, reported in just four genera (Boechera, Draba, Erysimum, and Parrya), and one intergeneric hybrid (Raphanobrassica). It is well studied only in Boechera, where it is widespread among 100+ recognized species. However, its occurrence in related genera of the tribe Boechereae has not been documented previously. Here we analyzed genome evolution, mode of reproduction, and fertility of the monospecific Boechereae genus Phoenicaulis (P. cheiranthoides), endemic to the northwestern United States. We discovered that the species encompasses diploid (2n = 2x = 14), triploid (2n = 3x = 21), and tetraploid (2n = 4x = 28) populations. Comparative chromosome painting analyses revealed that the three karyotypes are essentially structurally identical, differing only in the presence of a largely heterochromatic chromosome (Het) in the triploid and tetraploid cytotypes. The genome structure of Phoenicaulis appeared identical to that of Boechera species previously analyzed, suggesting genomic stasis despite the morphological and molecular divergence of the two genera. This genome colinearity extended to the presence and structure of the Het chromosomes, which are closely associated with apomictic reproduction in Boechera. Interestingly, all three cytotypes of Phoenicaulis proved to be apomictic, regardless of the presence or absence of a Het chromosome, and sexual populations have yet to be identified. 相似文献
7.
Geovani T. Ragagnin Larissa P. Bernardo Elgion L. S. Loreto 《Genetics and molecular biology》2016,39(1):145-150
Transposable elements (TEs) are nucleotide sequences found in most studied genomes. These elements are highly diversified and have a large variation in nucleotide structure and mechanisms of transposition. hobo is a member of class II, belonging to hAT superfamily, described inDrosophila melanogaster, and it presents in its Open Reading Frame, a repetitive region encoding the amino acids threonine-proline-glutamic acid (TPE), which shows variability in the number of repeats in some regions of the world. Due to this variability some evolutionary scenarios of the hobo element are discussed, such as the scenario of the invasion of hobo element in populations ofD. melanogaster. In the present study, we investigated 22 DNA sequences of D. melanogaster and seven sequences ofD. simulans, both from South America, to check the number of repetitions of TPE, in order to clarify the evolutionary scenario of thehobo element in these populations. Our results showed a monomorphism in populations of both species in South America, with only three TPE repeats. Hence, we discuss and propose an evolutionary scenario of the invasion of the hobo element in populations of D. melanogaster and D. simulans. 相似文献
8.
9.
Transposable elements (TEs) generate insertions and cause other mutations in the genomic DNA. It is proposed that during co-evolution
between TEs and eukaryotic genomes, an optimal path of the insertion mutagenesis is determined by the surviving TEs. These
TEs can become semi-permanently established, chromatin-regulated ‘source’ or ‘mutator genes’, responsible for targeting insertion
mutations to specific chromosomal regions. Such mutations can manifest themselves in non-random distribution patterns of interspersed
repeats in eukaryotic chromosomes. In this paper we discuss specific models, examples and implications of optimized mutagenesis
in eukaryotes.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
10.
Groth-Malonek M Wahrmund U Polsakiewicz M Knoop V 《Molecular biology and evolution》2007,24(4):1068-1074
Gene transfer from the mitochondrion into the nucleus is a corollary of the endosymbiont hypothesis. The frequent and independent transfer of genes for mitochondrial ribosomal proteins is well documented with many examples in angiosperms, whereas transfer of genes for components of the respiratory chain is a rarity. A notable exception is the nad7 gene, encoding subunit 7 of complex I, in the liverwort Marchantia polymorpha, which resides as a full-length, intron-carrying and transcribed, but nonspliced pseudogene in the chondriome, whereas its functional counterpart is nuclear encoded. To elucidate the patterns of pseudogene degeneration, we have investigated the mitochondrial nad7 locus in 12 other liverworts of broad phylogenetic distribution. We find that the mitochondrial nad7 gene is nonfunctional in 11 of them. However, the modes of pseudogene degeneration vary: whereas point mutations, accompanied by single-nucleotide indels, predominantly introduce stop codons into the reading frame in marchantiid liverworts, larger indels introduce frameshifts in the simple thalloid and leafy jungermanniid taxa. Most notably, however, the mitochondrial nad7 reading frame appears to be intact in the isolated liverwort genus Haplomitrium. Its functional expression is shown by cDNA analysis identifying typical RNA-editing events to reconstitute conserved codon identities and also confirming functional splicing of the 2 liverwort-specific group II introns. We interpret our results 1) to indicate the presence of a functional mitochondrial nad7 gene in the earliest land plants and strongly supporting a basal placement of Haplomitrium among the liverworts, 2) to indicate different modes of pseudogene degeneration and chondriome evolution in the later branching liverwort clades, 3) to suggest a surprisingly long maintenance of a nonfunctional gene in the presumed oldest group of land plants, and 4) to support the model of a secondary loss of RNA-editing activity in marchantiid liverworts. 相似文献
11.
WOLFGANG ARTHOFER SILVIO SCHÜLER FLORIAN M. STEINER BIRGIT C. SCHLICK‐STEINER 《Molecular ecology》2010,19(18):3853-3856
Ongoing genetic transfer from mitochondria and plastids into the nucleus is a well‐documented fact. While in metazoan molecular ecology the need for surveillance against pseudogene‐mediated artefacts when analysing mtDNA sequences is commonly accepted, no comparable measurements have been established for plastid‐based studies. We highlight the impact and management of nuclear mitochondrial insertions, argue that nuclear plastid sequences represent an underestimated but major factor in plant molecular ecology, and discuss potential avenues of remedy in chloroplast studies. 相似文献
12.
该研究比较了十字花科22个属22个物种的叶绿体基因组,以揭示十字花科叶绿体基因组的一般特征和变异特征。结果发现:(1)基因组大小为150kb左右,不同植物的叶绿体基因组之间存在1~5kb的差异,基因组大小的差异主要是大单拷贝(LSC)长度的差异引起的。(2)十字花科物种基因顺序基本一致,未检测到基因的重排和倒置事件。(3)trnY、trnG、ycf15、rps16基因在一些物种中发生丢失,petB、petD内含子序列也在个别物种内丢失。(4)基因组的4个边界相对保守,反向重复区a-大单拷贝区(IRa-LSC)边界处于rps19基因上,反向重复区a-小单拷贝区(IRa-SSC)边界在所有物种中均位于ycf1基因中,但是rps19和ycf1在边界两侧的长度具有差异,反向重复区b-小单拷贝区(IRb-SSC)边界在大部分物种中位于ycf1假基因和ndhF基因的重叠区内,而在庭荠(Alyssum desertorum)、小花南芥(Arabis alpina)2个物种中发生了改变,分别位于ycf1假基因和ndhF基因内。(5)29个蛋白编码基因长度发生变化,基因长度的变异来源于基因内含子或者编码区长度的改变,ycf1基因长度在3个物种中发生了大片段的缺失,部分基因长度的变化具有明显的系统发育信号。(6)基于叶绿体基因组数据构建的系统发育树具有较好的分辨率,各个进化分支具有较高的支持率。研究结果表明,利用叶绿体基因组数据可以为解决进化较快、系统发育分辨率低的植物类群的系统分类和系统发育关系提供更有力的证据。 相似文献
13.
Koch MA Dobes C Kiefer C Schmickl R Klimes L Lysak MA 《Molecular biology and evolution》2007,24(1):63-73
The occurrence of nonfunctional trnF pseudogenes has been rarely described in flowering plants. However, we describe the first large-scale supernetwork for the Brassiccaeae built from gene trees for 5 loci (adh, chs, matK, trnL-F, and ITS) and report multiple independent origins for trnF pseudogenes in crucifers. The duplicated regions of the original trnF gene are comprised of its anticodon domain and several other highly structured motifs not related to the original gene. Length variation of the trnL-F intergenic spacer region in different taxa ranges from 219 to 900 bp as a result of differences in pseudocopy number (1-14). It is speculated that functional constraints favor 2-3 or 5-6 copies, as found in Arabidopsis and Boechera. The phylogenetic distribution of microstructural changes for the trnL-F region supports ancient patterns of divergence in crucifer evolution for some but not all gene loci. 相似文献
14.
Mark W. Chase FLS Michael F. Fay FLS Joo‐Hwan Kim 《Botanical journal of the Linnean Society. Linnean Society of London》2016,181(4):567-584
Melanthiaceae (Liliales) comprise 17 genera of rhizomatous or bulbous perennials and are distributed across the Northern Hemisphere. The relationships among the five tribes in this family have been evaluated in many molecular and morphological studies. In this study, we performed a phylogenetic analysis of the 17 genera, including 106 species of Melanthiaceae sensu APG III and nine related species as outgroups, based on sequences of five plastid regions (atpB, rbcL, matK, ndhF and trnL‐F). Support values for the monophyly of the family (BSMP = 96%, BSML = 100%, PPBI = 1.00) and each tribe were improved in comparison with previous studies. Among the tribes, Melanthieae were sister to the remainder of the family and sister relationships between Xerophylleae and Parideae (BSMP = 96%, BSML = 100%, PPBI = 1.00) and Chionographideae and Heloniadeae (BSMP = 96%, BSML = 100%, PPBI = 1.00) were confirmed. Notably, the generic concept of Veratrum s.l. including Melanthium was not supported in the present study and these genera should be treated as distinct. In the case of Parideae, the relationship of Trillium govanianum to the other species remains uncertain and requires further studies. Finally, we mapped seven representative morphological characters onto the molecular phylogenetic tree for Melanthiaceae. 相似文献
15.
Schmidt AL Anderson LM 《Biological reviews of the Cambridge Philosophical Society》2006,81(4):531-543
There is no logical or theoretical barrier to the proposition that organismal and cell signaling could transduce environmental signals into specific, beneficial changes in primary structure of noncoding DNA via repetitive element movement or mutation. Repetitive DNA elements, including transposons and microsatellites, are known to influence the structure and expression of protein-coding genes, and to be responsive to environmental signals in some cases. These effects may create fodder for adaptive evolution, at rates exceeding those observed for point mutations. In many cases, the changes are no doubt random, and fitness is increased through simple natural selection. However, some transposons insert at specific sites, and certain regions of the genome exhibit selectively and beneficially high mutation rates in a range of organisms. In multicellular organisms, this could benefit individuals in situations with significant potential for clonal expansion: early life stages or regenerative tissues in animals, and most plant tissues. Transmission of the change to the next generation could occur in plants and, under some circumstances, in animals. 相似文献
16.
人类基因组上的假基因 总被引:5,自引:0,他引:5
假基因是基因组上与编码基因序列非常相似的非功能性基因组DNA拷贝,一般情况都不被转录,且没有明确生理意义。假基因根据其来源可分为复制假基因和已加工假基因。迄今为止,明确鉴定的人类假基因多为已加工假基因,有8000个之多。在Swiss-Prot/TrEMBL收录的编码蛋白质的将近25500个基因序列中,约10%在基因组中有一个或多个近全长已加工假基因。其余的功能基因都没有已加工假基因。核糖体蛋白基因具有最多数量的已加工假基因,约有l700个(占已加工假基因数的22%),少数基因,如cyclophilinA、肌动蛋白(actin)、角蛋白(keratin)、GAPDH、细胞色素C(cytochromec)和nucleophosmin等则有很多份已加工假基因。总体上讲,假基因在人类染色体上的分布与染色体长度成比例,但已加工假基因在GC含量为41%~46%的染色体区域密度最高。已加工假基因的拷贝数和功能基因在生殖器官中的表达高度一致,说明许多假基因发生在胚胎阶段,另外也和基因中GC含量和基因大小密切相关。假基因的准确鉴定对基因组进化、分子医学研究和医学应用具有重要意义。 相似文献
17.
Petrov DA Aminetzach YT Davis JC Bensasson D Hirsh AE 《Molecular biology and evolution》2003,20(6):880-892
The Drosophila melanogaster genome contains approximately 100 distinct families of transposable elements (TEs). In the euchromatic part of the genome, each family is present in a small number of copies (5-150 copies), with individual copies of TEs often present at very low frequencies in populations. This pattern is likely to reflect a balance between the inflow of TEs by transposition and the removal of TEs by natural selection. The nature of natural selection acting against TEs remains controversial. We provide evidence that selection against chromosome abnormalities caused by ectopic recombination limits the spread of some TEs. We also demonstrate for the first time that some TE families in the Drosophila euchromatin appear to be only marginally affected by purifying selection and contain many copies at high population frequencies. We argue that TEs in these families attain high population frequencies and even reach fixation as a result of low family-wide transposition rates leading to low TE copy numbers and consequently reduced strength of selection acting on individual TE copies. Fixation of TEs in these families should provide an upward pressure on the size of intergenic sequences counterbalancing rapid DNA loss through small deletions. Copy-number-dependent selection on TE families caused by ectopic recombination may also promote diversity among TEs in the Drosophila genome. 相似文献
18.
Complete Nucleotide Sequence of the Chloroplast Genome from the Tasmanian Blue Gum, Eucalyptus globulus (Myrtaceae) 总被引:1,自引:0,他引:1
The complete nucleotide sequence of the chloroplast genome ofthe hardwood species Eucalyptus globulus is presented and comparedwith chloroplast genomes of tree and non-tree angiosperms andtwo softwood tree species. The 160 286 bp genome is similarin gene order to that of Nicotiana, with an inverted repeat(IR) (26 393 bp) separated by a large single copy (LSC) regionof 89 012 bp and a small single copy region of 18 488 bp. Thereare 128 genes (112 individual gene species and 16 genes duplicatedin the inverted repeat) coding for 30 transfer RNAs, 4 ribosomalRNAs and 78 proteins. One pseudogene (-infA) and one pseudo-ycf(-ycf15) were identified. The chloroplast genome of E. globulusis essentially co-linear with that of another hardwood treespecies, Populus trichocarpa, except that the latter lacks rps16and rpl32, and the IR has expanded in Populus to include rps19(part of the LSC in E. globulus). Since the chloroplast genomeof E. globulus is not significantly different from other treeand non-tree angiosperm taxa, a comparison of hardwood and softwoodchloroplasts becomes, in essence, a comparison of angiospermand gymnosperm chloroplasts. When compared with E. globulus,Pinus chloroplasts have a very small IR, two extra tRNAs andfour additional photosynthetic genes, lack any functional ndhgenes and have a significantly different genome arrangement.There does not appear to be any correlation between plant habitand chloroplast genome composition and arrangement. 相似文献
19.
20.
The origin and evolution of the thousands of species-specific genes with unknown functions, the so-called orphan genes, has been a mystery. Here, we have studied the rates and patterns of orphan sequence evolution, using the Rickettsia as our reference system. Of the Rickettsia conorii orphans examined in this study, 80% were found to be short gene fragments or fusions of short segments from neighboring genes. We reconstructed the putative sequences of the full-length genes from which the short orphan fragments are thought to have originated. One of the genes thus reconstructed displays weak similarity to the ankyrin-repeat protein family, an identification that is strongly supported by comparative molecular modeling. Studies of the patterns of gene fragmentation underscore the importance of short repeated sequences as targets for recombination events that result in sequence loss and the formation of short, transient open reading frames. Our analysis demonstrates that gene sequences present in the common ancestor can be inferred even in cases when no full-length open reading frame is present in any of the contemporary species. Such reconstructions support the identification of lost protein functions and hint at important lifestyle changes. 相似文献