scholarly journals The Molecular Phylogeny of the New Zealand Endemic Genus Hadramphus and the Revival of the Genus Karocolens

Diversity ◽  
2018 ◽  
Vol 10 (3) ◽  
pp. 88
Author(s):  
Emily Fountain ◽  
Robert Cruickshank ◽  
Adrian Paterson
Keyword(s):  
New Zealand ◽  
Gene Sequence ◽  
Mitochondrial Gene ◽  
Single Gene ◽  
Morphological Characteristics ◽  
Nuclear Gene ◽  
Similar Species ◽  
Morphological Similarity ◽  
Coalescent Approach ◽  
Systematic Relationships

The delineation of species is important to the fields of evolution, ecology and conservation. The use of only a single line of evidence, e.g., morphology or a single gene sequence, may underestimate or overestimate the level of diversity within a taxon. This problem often occurs when organisms are morphologically similar but genetically different, i.e., for cryptic species. The Hadramphus genus contains four endangered, morphologically similar species of weevils, each endemic to a specific New Zealand region (Hadramphus spinipennis Chatham Islands, H. stilbocarpae Fiordland, H. tuberculatus McKenzie Country, H. pittospori Poor Knights Islands). The systematic relationships among these species are unclear. We used samples from these species and a closely related genus, Lyperobius huttoni, to obtain data from the mitochondrial gene cytochrome c oxidase subunit I and the nuclear gene internal transcribe spacer 2. In addition to the multi-locus coalescent approach, we modelled morphological characteristics combined with the genetic data. We found that H. spinipennis, H. tuberculatus and H. stilbocarpae were a closely related clade. Despite a strong morphological similarity, Hadramphus pittospori was found to be genetically distinct from the other Hadramphus species, which supports the resurrection of the monotypic genus Karocolens for this species.

scholarly journals Cosegregation of Single Genes Associated with Fertility Restoration and Transcript Processing of Sorghum Mitochondrial orf107 and urf209

Genetics ◽  
1998 ◽  
Vol 150 (1) ◽  
pp. 383-391 ◽  
Author(s):  
Hoang V Tang ◽  
Ruying Chang ◽  
Daryl R Pring
Keyword(s):  
Fertility Restoration ◽  
Mitochondrial Gene ◽  
Pollen Viability ◽  
Single Gene ◽  
Dominant Gene ◽  
Nuclear Gene ◽  
Male Sterile ◽  
Reading Frame ◽  
Transcript Processing ◽  
Backcross Populations

Abstract Defective nuclear-cytoplasmic interactions leading to aberrant microgametogenesis in sorghum carrying the IS1112C male-sterile cytoplasm occur very late in pollen maturation. Amelioration of this condition, the restoration of pollen viability, involves a novel two-gene gametophytic system, wherein genes designated Rf3 and Rf4 are required for viability of individual gametes. Rf3 is tightly linked to, or represents, a single gene that regulates a transcript processing activity that cleaves transcriptsof orf107, a chimeric mitochondrial open reading frame specific to IS1112C. The mitochondrial gene urf 209 is also subject to nucleus-specific enhanced transcript processing, 5′ to the gene, conferred by a single dominant gene designated Mmt1. Examinations of transcript patterns in F2 and two backcross populations indicated cosegregation of the augmented orf107 and urf209 processing activities in IS1112C. Several sorghum lines that do not restore fertility or confer orf107 transcript processing do exhibit urf209 transcript processing, indicating that the activities are distinguishable. We conclude that the nuclear gene(s) conferring enhanced orf107 and urf209 processing activities are tightly linked in IS1112C. Alternatively, the similarity in apparent regulatory action of the genes may indicate allelic differences wherein the IS1112C Rf3 allele may differ from alleles of maintainer lines by the capability to regulate both orf107 and urf209 processing activities.

scholarly journals Gene Sequence Analysis of Mitochondrial COI in Genus Saperda (Coleoptera: Cerambycidae: Lamiinae)

2021 ◽  
Author(s):  
Wei XU ◽  
Qinhua Gan ◽  
Jian Pu ◽  
Yingwen Pan ◽  
Bo Cai ◽  
...  
Keyword(s):  
Sequence Analysis ◽  
Detection Rate ◽  
Gene Sequence ◽  
Mitochondrial Gene ◽  
Dna Barcode ◽  
Nuclear Gene ◽  
Rapid Identification ◽  
Mitochondrial Coi ◽  
Gene Sequence Analysis ◽  
Total Dna

In this study, the total DNA of nine species of Saperda (Lopezcolonia) octopunctata (Scopoli, 1772), Saperda (Lopezcolonia) scalaris (Linnaeus, 1758), Saperda interrupta Gebler, Saperda Alberti (Plavilstshikov), Saperda (Saperda) similis Laicharting, 1784, Saperda (Compsidia) populnea (Linnaeus, 1758), Saperda (Saperda) carcharias (Linnaeus, 1758), Saperda (Lopezcolonia) perforata Pallas, 1773 and Saperda ohbayashi were extracted. Two partial sequences of mitochondrial gene and one partial sequence of nuclear gene were amplified. Comparing the COI sequence with the DNA barcode data in GenBank can effectively identify the related species of Saperda. It will be applied to the rapid identification of some species of Saperda in imported wood at ports, and improve the detection rate of plant quarantine.

scholarly journals Phylogeography of the New Zealand whelks Cominella maculosa and C. virgata

2021 ◽  
Author(s):  
◽  
Kerry Walton
Keyword(s):  
New Zealand ◽  
Dna Sequences ◽  
High Frequency ◽  
Phylogenetic Analyses ◽  
Mitochondrial Gene ◽  
Nuclear Gene ◽  
Disjunct Distribution ◽  
Phylogeographic Structure ◽  
Interglacial Period ◽  
Cook Strait

<p>Cominella maculosa and C. virgata are common rocky shore whelk species from New Zealand. This study used DNA sequences from the mitochondrial gene cytochrome c oxidase subunit 1 (CO1) to expand an earlier unpublished dataset and examine the phylogeographic structure of both species in the Cook Strait region, of C. maculosa in the Chatham Islands, and of C. virgata in the northern North Island. Both species are found to have a considerable degree of phylogeographic structure, concordant with that reported by an earlier study and for other species with direct development.  South Island sites sampled for C. maculosa had several private haplotypes and a high frequency haplotype that is shared with populations from the southern North Island. Together, these formed a ‘southern haplogroup’. Low diversity in ‘southern’ populations may reflect founder effects that would have occurred as part of a southward range expansion during the onset of the present interglacial period. The Chatham Islands samples had two haplotypes that formed a separate sub-group to the ‘southern haplogroup’, suggesting Chatham Islands populations are moderately isolated from those on mainland New Zealand but may have been founded from ‘southern’ populations relatively recently.  The high frequency haplotype present in South Island samples of C. virgata is absent in Wellington samples but widespread in those from the north-eastern North Island. South Island populations may have been founded from the Hauraki Gulf through human-mediated translocation events. Phylogenetic analyses with a focus on C. virgata were conducted using the mitochondrial genes CO1 and 16SrRNA, and the nuclear gene 18S rRNA, to expand an earlier published dataset. The purported northern subspecies C. virgata brookesi does not form a monophyletic lineage and voucher specimens fluidly intergrade with the nominal subspecies, with which it is synonymised. A lectotype is designated for Buccinum lineolatum Quoy & Gaimard, 1833, for which Cominella virgata is a replacement name. Potential causes of the disjunct distribution patterns of C. virgata and other mollusc taxa are discussed with particular reference to the formation and timing of marine straits through the Auckland Isthmus and Cook Strait.</p>

scholarly journals Phylogeography of the New Zealand whelks Cominella maculosa and C. virgata

2021 ◽  
Author(s):  
◽  
Kerry Walton
Keyword(s):  
New Zealand ◽  
Dna Sequences ◽  
High Frequency ◽  
Phylogenetic Analyses ◽  
Mitochondrial Gene ◽  
Nuclear Gene ◽  
Disjunct Distribution ◽  
Phylogeographic Structure ◽  
Interglacial Period ◽  
Cook Strait

<p>Cominella maculosa and C. virgata are common rocky shore whelk species from New Zealand. This study used DNA sequences from the mitochondrial gene cytochrome c oxidase subunit 1 (CO1) to expand an earlier unpublished dataset and examine the phylogeographic structure of both species in the Cook Strait region, of C. maculosa in the Chatham Islands, and of C. virgata in the northern North Island. Both species are found to have a considerable degree of phylogeographic structure, concordant with that reported by an earlier study and for other species with direct development.  South Island sites sampled for C. maculosa had several private haplotypes and a high frequency haplotype that is shared with populations from the southern North Island. Together, these formed a ‘southern haplogroup’. Low diversity in ‘southern’ populations may reflect founder effects that would have occurred as part of a southward range expansion during the onset of the present interglacial period. The Chatham Islands samples had two haplotypes that formed a separate sub-group to the ‘southern haplogroup’, suggesting Chatham Islands populations are moderately isolated from those on mainland New Zealand but may have been founded from ‘southern’ populations relatively recently.  The high frequency haplotype present in South Island samples of C. virgata is absent in Wellington samples but widespread in those from the north-eastern North Island. South Island populations may have been founded from the Hauraki Gulf through human-mediated translocation events. Phylogenetic analyses with a focus on C. virgata were conducted using the mitochondrial genes CO1 and 16SrRNA, and the nuclear gene 18S rRNA, to expand an earlier published dataset. The purported northern subspecies C. virgata brookesi does not form a monophyletic lineage and voucher specimens fluidly intergrade with the nominal subspecies, with which it is synonymised. A lectotype is designated for Buccinum lineolatum Quoy & Gaimard, 1833, for which Cominella virgata is a replacement name. Potential causes of the disjunct distribution patterns of C. virgata and other mollusc taxa are discussed with particular reference to the formation and timing of marine straits through the Auckland Isthmus and Cook Strait.</p>

scholarly journals SNP and SCAR Markers for Specific Discrimination of Antler-Shaped Ganoderma lucidum

2019 ◽  
Vol 7 (1) ◽  
pp. 12 ◽  
Author(s):  
O-Chul Kwon ◽  
Chang-Soo Lee ◽  
Young-Jin Park
Keyword(s):  
Ganoderma Lucidum ◽  
Gene Sequence ◽  
Rapd Analysis ◽  
Random Amplified Polymorphic Dna ◽  
Morphological Characteristics ◽  
Pcr Analysis ◽  
Scar Markers ◽  
Nucleotide Polymorphism ◽  
Single Nucleotide ◽  
Specific Fragment

In this study we identified single nucleotide polymorphism (SNP) and sequence characteristic amplification region (SCAR) markers for specific identification of antler-shaped Ganoderma lucidum strains. When the partial mitochondrial SSU rDNA gene sequence of various antler- and kidney-shaped G. lucidum strains were analyzed and aligned, an SNP was found only in the antler-shaped G. lucidum strain at position 456 bp. In addition, this SNP of antler-shaped strains was digested by HinfI restriction enzyme. We further analyzed the polymorphism of various G. lucidum strains by random amplified polymorphic DNA (RAPD) analysis. In RAPD analysis, we isolated and sequenced a fragment, specific for antler-shaped G. lucidum strains. Based on this specific fragment sequence, two sets of specific primer pairs for antler-shaped G. lucidum strains were designed. PCR analysis revealed that two specific bands were observed only from antler-shaped strains. These two molecular markers will be helpful for identification of morphological characteristics of G. lucidum.

scholarly journals BAGET 2.0: an updated web tool for the effortless retrieval of prokaryotic gene context and sequence

2021 ◽  
Author(s):  
Benjamin Hepp ◽  
Violette Da Cunha ◽  
Florence Lorieux ◽  
Jacques Oberto
Keyword(s):  
Gene Sequence ◽  
Single Gene ◽  
Daily Basis ◽  
Web Tool ◽  
Web Based ◽  
Internet Explorer ◽  
Prokaryotic Genomes ◽  
Exploration Tool ◽  
Genome Browsers ◽  
Archaeal Gene

Abstract Motivation The retrieval of a single gene sequence and context from completely sequenced bacterial and archaeal genomes constitutes an intimidating task for the wet bench biologist. Existing web-based genome browsers are either too complex for routine use or only provide a subset of the available prokaryotic genomes. Results We have developed BAGET 2.0 (Bacterial and Archaeal Gene Exploration Tool), an updated web service granting access in just three mouse clicks to the sequence and synteny of any gene from completely sequenced bacteria and archaea. User-provided annotated genomes can be processed as well. BAGET 2.0 relies on a local database updated on a daily basis. Availability and implementation BAGET 2.0 befits all current browsers such as Chrome, Firefox, Edge, Opera and Safari. Internet Explorer 11 is supported. BAGET 2.0 is freely accessible at https://archaea.i2bc.paris-saclay.fr/baget/

Yeast CBP1 mRNA 3' end formation is regulated during the induction of mitochondrial function

1991 ◽  
Vol 11 (2) ◽  
pp. 813-821
Author(s):  
S A Mayer ◽  
C L Dieckmann
Keyword(s):  
Mitochondrial Function ◽  
Developmental Stages ◽  
Single Gene ◽  
Mitochondrial Protein ◽  
Nuclear Gene ◽  
State Level ◽  
Yeast Cells ◽  
Cdna Clones ◽  
Coding Sequence ◽  
Polyadenylation Sites

Alternative mRNA processing is one mechanism for generating two or more polypeptides from a single gene. While many mammalian genes contain multiple mRNA 3' cleavage and polyadenylation signals that change the coding sequence of the mature mRNA when used at different developmental stages or in different tissues, only one yeast gene has been identified with this capacity. The Saccharomyces cerevisiae nuclear gene CPB1 encodes a mitochondrial protein that is required for cytochrome b mRNA stability. This 66-kDa protein is encoded by a 2.2-kb mRNA transcribed from CPB1. Previously we showed that a second 1.2-kb transcript is initiated at the CBP1 promoter but has a 3' end near the middle of the coding sequence. Furthermore, it was shown that the ratio of the steady-state level of 2.2-kb CBP1 message to 1.2-kb message decreases 10-fold during the induction of mitochondrial function, while the combined levels of both messages remain constant. Having proposed that regulation of 3' end formation dictates the amount of each CBP1 transcript, we now show that a 146-bp fragment from the middle of CBP1 is sufficient to direct carbon source-regulated production of two transcripts when inserted into the yeast URA3 gene. This fragment contains seven polyadenylation sites for the wild-type 1.2-kb mRNA, as mapped by sequence analysis of CBP1 cDNA clones. Deletion mutations upstream of the polyadenylation sites abolished formation of the 1.2-kb transcript, whereas deletion of three of the sites only led to a reduction in abundance of the 1.2-kb mRNA. Our results indicate that regulation of the abundance of both CBP1 transcripts is controlled by elements in a short segment of the gene that directs 3' end formation of the 1.2-kb transcript, a unique case in yeast cells.

In vivo analysis of sequences necessary for CBP1-dependent accumulation of cytochrome b transcripts in yeast mitochondria

1993 ◽  
Vol 13 (7) ◽  
pp. 4203-4213
Author(s):  
T M Mittelmeier ◽  
C L Dieckmann
Keyword(s):  
Cytochrome B ◽  
Mitochondrial Gene ◽  
Microprojectile Bombardment ◽  
Nuclear Gene ◽  
State Level ◽  
Transcription Unit ◽  
Endonucleolytic Cleavage ◽  
In Vivo Analysis ◽  
Nucleotide Region

In Saccharomyces cerevisiae, cytochrome b, an essential component of the respiratory chain, is encoded by the mitochondrial gene cob. The cob transcription unit includes the tRNA(Glu) gene from positions -1170 to -1099 relative to the cob ATG at +1. The initial tRNA(Glu)-cob transcript undergoes several processing events, including removal of tRNA(Glu) and production of the mature 5' end of cob mRNA at nucleotide -954. The nuclear gene product CBP1 is specifically required for the accumulation of cob mRNA. In cbp1 mutant strains, cob transcripts are not detectable by Northern (RNA) blot analysis, but the steady-state level of tRNA(Glu) is similar to that of wild type. The results of a previous study led to the conclusion that a 400-nucleotide region just downstream of tRNA(Glu) is sufficient for CBP1 function. In the present study, the microprojectile bombardment method of mitochondrial transformation was used to introduce deletions within this region of cob. The analysis of cob transcripts in strains carrying the mitochondrial deletion genomes indicates that a 63-nucleotide sequence that encompasses the cleavage site at -954 is sufficient both for CBP1 function and for correct positioning of the cleavage. Furthermore, the data indicate that CBP1 prevents the degradation of unprocessed cob transcripts produced by endonucleolytic cleavage at the 3' end of tRNA(Glu).

Three new species of semi-aquatic freshwater earthworms of the genus Glyphidrilus Horst, 1889 from Malaysia (Clitellata: Oligochaeta: Almidae)

Zootaxa ◽  
2012 ◽  
Vol 3458 (1) ◽  
pp. 120 ◽  
Author(s):  
RATMANEE CHANABUN ◽  
CHIRASAK SUTCHARIT ◽  
PIYOROS TONGKERD ◽  
SHAU-HWAI AILEEN TAN ◽  
SOMSAK PANHA
Keyword(s):  
New Species ◽  
Morphological Characteristics ◽  
Similar Species ◽  
Three New Species

Three new species of semi-aquatic freshwater earthworms of the genus Glyphidrilus Horst, 1889 are described from Malaysia.Glyphidrilus bisegmentus sp. n. was collected from Air Banun Pandig, Perak, Glyphidrilus kotatinggi sp. n. from Kota Tinggiwaterfall, Johor, and Glyphidrilus peninsularis sp. n. from Sungei Bantang, Johor. For comparison, type and non-type materialof five morphologically similar species was reinvestigated. The descriptions of the new species include illustrations of the external and internal morphological characteristics.

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