st6gal2 gene (Marinus)
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St6gal2 Gene, supplied by Marinus, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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1) Product Images from "Molecular Phylogeny and Functional Genomics of ?-Galactoside ?2,6-Sialyltransferases That Explain Ubiquitous Expression of st6gal1 Gene in Amniotes * "
Article Title: Molecular Phylogeny and Functional Genomics of ?-Galactoside ?2,6-Sialyltransferases That Explain Ubiquitous Expression of st6gal1 Gene in Amniotes
Journal: The Journal of Biological Chemistry
doi: 10.1074/jbc.M110.163931
Figure Legend Snippet: A, ML phylogenetic tree of 36 sialyltransferases of the ST6Gal family. A maximum likelihood phylogenetic tree was inferred by the Phyml, JTT model of amino acid substitution: 36 ST6Gal sequences, 11 vertebrate ST6Gal I, 11 vertebrate ST6Gal II. G-BLOCKS selected 200 positions. Bootstrap values were calculated from 500 replicates, and values of >50% are reported at the left of each divergence point. The tree is rooted with the invertebrate arthropod sequences as the outgroup. B, calculation of divergence time between ST6Gal I and ST6Gal II. The lengths of each horizontal branch were calculated from the linearized tree obtained with ME (Min. Evol.) using MEGA4.0.
Techniques Used:
Figure Legend Snippet: Indel insertion/deletion events in the ST6Gal I and ST6Gal II protein sequences. A, alignments of protein sequences without gap are schematized in gray; indels are indicated by white boxes. Intron insertions are indicated by black bars in the teleost st6gal1 sequence. B, simplified phylogenetic tree and insertion/deletion distribution. The tree was constructed with 200 positions within the catalytic domain, using ME. Filled square, insertion; open squares, indel; filled rectangles, intron insertion; open triangles, deletion. C, correlation between Indel numbers and branch lengths. The tree was constructed as in B. The regression equation was given by PAST 2.01.
Techniques Used: Sequencing, Construct
Figure Legend Snippet: Genomic organization of human st6gal1/st6gal2 cluster paralogon and putative orthologous counterpart is indicative of a WGD event. Eleven putative paralogous genes spanning regions on human chromosomes HSA2q11.3 and HSA3q27 were found. Genes represented were chosen from analysis performed at Ensembl by chromosomal walking and reciprocal TBLASTN searches of genes adjacent to st6gal loci.
Techniques Used:
Figure Legend Snippet: Syntenic relationships of the st6gal gene loci in vertebrate and amphioxus genomes. Physically mapped genomes of human (HSA), mouse (MMU), chicken (GGA), O. latipes (OLA), T. nigroviridis (TNI), G. aculeatus (GAC), and D. rerio (DRE) in Ensembl were used to identify conserved gene neighbors of the st6gal genes. A, conserved syntenic blocks found around the st6gal2 gene; B, disrupted synteny around the st6gal1 gene found in amniotes and in teleost genomes. C, schematic diagram depicting the genetic events that occurred early in the jawed vertebrate lineage and led to modern st6gal genes in fish. The last common ancestor (LCA) of teleost fishes and amniotes around 500 MYA bore an ancestral st6gal gene designated the st6gal1/2 gene, which was located on the protochromosome DRE 15-2-6-9 HSA 2-3; WGD R2 (∼475 MYA) gave rise to st6gal1 and st6gal2 genes found on HSA3 and HSA2, respectively, and on the protochromosome DRE 15-2 and DRE 6-9 of the teleost last common ancestor. The DRE 2/DRE 15 and DRE 6/DRE 9 pairs of chromosomes derived from these single common protochromosomes DRE 15-2 and DRE 6-9 after WGD R3. Rearrangement of a block of genes including st6gal1 occurred in teleosts, resulting in the translocation of st6gal1 on DRE21, whereas the other duplicate, named st6gal1-r, disappeared from DRE 15 through pseudogenization or deletion. st6gal2 and st6gal2-r were maintained on DRE 6 and DRE 9. D, conserved synteny observed between the amphioxus genomic region hosting the st6gal-like gene (scaf V2 104q) and the two sets of human paralogons described in the legend to Fig. 3.
Techniques Used: Derivative Assay, Blocking Assay, Translocation Assay
Figure Legend Snippet: Expression pattern of the zebrafish and amphibian st6gal genes in various adult tissues using RT-PCR. A, fish st6gal genes. Relative expression levels of zebrafish st6gal and β-actin mRNA were evaluated by RT-PCR as described under “Experimental Procedures,” among various adult tissues. Oligonucleotide primer sequences specific to fish st6gal1, st6gal2, and st6gal2-r are given in supplemental Fig. 5 and yield 896-, 628-, and 299-bp PCR fragments, respectively. Lane 1, kidney; lane 2, intestine; lane 3, brain; lane 4, liver; lane 5, muscle; lane 6, heart; lane 7, eggs; lane 8, oocytes. The zebrafish β-actin (378 bp) was amplified as a control of cDNA synthesis and purity. B, amphibian st6gal genes. Oligonucleotides specific to S. tropicalis st6gal1 and st6gal2 are indicated in supplemental Fig. 5 and yield 236- and 465-bp PCR fragments, respectively. Lane 1, muscle; lane 2, eyes; lane 3, heart; lane 4, skin; lane 5, lung; lane 6, stomach; lane 7, ovaries; lane 8, intestine; lane 9, liver; lane 10, brain; lane 11, kidney. The amphibian β-catenin (327 bp) was amplified for 35 cycles as a control of cDNA synthesis and purity.
Techniques Used: Expressing, Reverse Transcription Polymerase Chain Reaction, Amplification, Control, cDNA Synthesis
Figure Legend Snippet: Expression pattern of the zebrafish st6gal genes during zebrafish embryonic development using whole mount ISH at early developmental stages (A) and later developmental stages (B). The st6gal1 gene shows no labeling at early developmental stages (gastrula (G), early somitogenesis (ES), and middle somitogenesis (MS)). st6gal1 is found in the ventricular part of telencephalon, in the ventral part of diencephalon, in the lateral part of the hindbrain (discontinuous patches of cells), and in the lateral part of the spinal cord at 24 and 36 hpf. st6gal1 gene expression is detected in the ganglion cell layer of the retina (except in the proliferative zone), cranial ganglia, and brain marginal zone at 48 hpf and is not detected later. The st6gal2 gene is expressed at the gastrula stage in the prechordal plate mesendoderm and at early somitogenesis in polster, anterior border of neural plate, adaxial cells, formed somites, and also weakly in segmental plates. At middle somitogenesis, it is expressed in polster, anterior head epidermis, caudal adaxial cells, and the last formed somites. At 24 hpf, the st6gal2 gene is expressed in tail somites and adaxial cells and weakly in the CNS; later, at 36 hpf, a stronger signal is found in the marginal zone, and no labeling is detected in tectum. At 48 hpf and 5 days postfertilization, the st6gal2 transcript is detected in anterior diencephalon and in the ganglion cell layer of retina but not in the proliferative zone. The st6gal2-r gene is weakly expressed at the gastrula stage and shows also a weak basal level of expression at early somitogenesis and middle somitogenesis and more labeling in hatching glands. At later developmental stages, from pharyngula to larva stages (24 hpf to 5 days postfertilization (dpf)), the st6gal2-r gene is detected in hatching glands, mucus cells, proctodeum, intestinal bulb, gall bladder, inner nuclear cell layer of retina (except in the proliferative zone), nucleus in diencephalon, nucleus in anterior tectum, and nucleus in hindbrain at the larval stage. hg, hatching gland; inl of retina, inner nuclear layer of retina; i bulb, intestinal bulb; n in diencephalon, nucleus in diencephalon; n in ant tectum, nucleus in anterior tectum; n in hb, nucleus in hindbrain; up mesoderm, unsegmented paraxial mesoderm; tg, tegmentum; ventral dc, ventral diencephalon. LV, lateral view; DV, dorsal view.
Techniques Used: Expressing, Labeling, Gene Expression
![a Illustration shows pathways involved in sialic acid and sialylated glycans biosynthesis. Relative expression for each gene was extracted from bulk RNA-Seq data comparing naive and arthritic SFs directly isolated from mouse synovium. b Synovial fibroblasts expanded from healthy or arthritic mouse joints were stimulated in vitro for 6 h with recombinant IL-1β, TNF, or IL-17A [10 ng/ml]. mRNA expression for genes involved in sialylation [as shown in a ] was evaluated by RT-qPCR. Il6 was included as a positive control to confirm cell activation. Volcano plots show log2 fold difference in stimulated cells ( x axis) and p -value ( y axis). Each dot represents the mean of three independent experiments analyzed in triplicate, with naive cells in blue and arthritic cells in red. The pink line indicates a twofold-change in gene expression threshold and blue lines indicate p = 0.05 threshold in the t -test to evaluate statistical significance. c TNF, but not IL-1β or IL-17A reduces α2-6-sialylation of synovial fibroblasts both at RNA ( St6gal1 expression) and protein (SNA binding) levels. Expression of St6gal1 (left panel ) was evaluated by RT-qPCR. Results show the mean of three independent experiments analyzed in triplicate, error bars represent SEM. Statistical significance was determined using two-tail unpaired t -tests where * p < 0.05 and ** p < 0.01. Actual p -values: a 0.0069, b 0.0277. Expression of α2-6 sialylated glycoconjugates was determined by SNA binding (right panel) as in Fig. . Results are merged from 3 (naive) and 2 (CIA) independent experiments, n = 10 (DMEM naive), 16 (IL-1 naive and IL-17 naive), 13 (TNF naive), 10 (DMEM CIA), 12 (IL-1 naive and IL-17 naive), and 9 (TNF CIA). Statistical significance was determined using two-tail unpaired t -tests, where ** p < 0.01 and *** p < 0.001. Actual p -values: c 0.0124, d 0.0091. d SFs were expanded from OA human synovium. Cells were stimulated with recombinant human TNF (10 ng/ml) for 6 h. IL6 , ST6GAL1, and <t>ST6GAL2</t> expression were determined by qPCR. Results show relative expression to HPRT, showing mean ± SEM. Statistics: one-tail unpaired t -test, n = 3 biological replicates from cells pooled from three donors, *** p < 0.001, * p < 0.05. Actual p -values: e <0.0001, f 0.0170, g 0.0321. e Relative expression of individual sialylated glycan structures was evaluated by MALDI-TOF MS analysis as in Fig. . Ratios of sialylated vs non-sialylated twin structures were evaluated for non-stimulated cells (blue) and TNF stimulated (red) cells (48 h, 10 ng/ml). Results are from one single experiment using pooled cells from three animals.](https://pub-med-central-images-cdn.bioz.com/pub_med_central_ids_ending_with_8094/pmc08058094/pmc08058094__41467_2021_22365_Fig5_HTML.jpg)