Mouse Slit1 Conditional Knockout Project (CRISPR/Cas9)
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From Bipotent Neuromesodermal Progenitors to Neural-Mesodermal Interactions During Embryonic Development
International Journal of Molecular Sciences Review From Bipotent Neuromesodermal Progenitors to Neural-Mesodermal Interactions during Embryonic Development Nitza Kahane and Chaya Kalcheim * Department of Medical Neurobiology, Institute of Medical Research Israel-Canada (IMRIC) and the Edmond and Lily Safra Center for Brain Sciences (ELSC), Hebrew University of Jerusalem-Hadassah Medical School, P.O. Box 12272, Jerusalem 9112102, Israel; [email protected] * Correspondence: [email protected] Abstract: To ensure the formation of a properly patterned embryo, multiple processes must operate harmoniously at sequential phases of development. This is implemented by mutual interactions between cells and tissues that together regulate the segregation and specification of cells, their growth and morphogenesis. The formation of the spinal cord and paraxial mesoderm derivatives exquisitely illustrate these processes. Following early gastrulation, while the vertebrate body elongates, a pop- ulation of bipotent neuromesodermal progenitors resident in the posterior region of the embryo generate both neural and mesodermal lineages. At later stages, the somitic mesoderm regulates aspects of neural patterning and differentiation of both central and peripheral neural progenitors. Reciprocally, neural precursors influence the paraxial mesoderm to regulate somite-derived myogen- esis and additional processes by distinct mechanisms. Central to this crosstalk is the activity of the axial notochord, which, via sonic hedgehog signaling, plays pivotal roles in neural, skeletal muscle and cartilage ontogeny. Here, we discuss the cellular and molecular basis underlying this complex Citation: Kahane, N.; Kalcheim, C. developmental plan, with a focus on the logic of sonic hedgehog activities in the coordination of the From Bipotent Neuromesodermal Progenitors to Neural-Mesodermal neural-mesodermal axis. -
Slit1 and Slit2 Cooperate to Prevent Premature Midline Crossing of Retinal Axons in the Mouse Visual System
Neuron, Vol. 33, 219–232, January 17, 2002, Copyright 2002 by Cell Press Slit1 and Slit2 Cooperate to Prevent Premature Midline Crossing of Retinal Axons in the Mouse Visual System Andrew S. Plump,1,2,6 Lynda Erskine,3,6,7 midbrain. Some axons do not cross, projecting to the Christelle Sabatier,1 Katja Brose,1 same targets but ipsilaterally. As with many other brain Charles J. Epstein,2 Corey S. Goodman,4 commissures, formation of the optic chiasm occurs at Carol A. Mason,3 and Marc Tessier-Lavigne1,5,8 an invariant position along the antero-posterior axis of 1 Departments of Anatomy and the developing forebrain. Mechanisms must therefore of Biochemistry and Biophysics exist not only to direct divergence at the midline but also Howard Hughes Medical Institute to prevent retinal axons from crossing at inappropriate 2 Division of Medical Genetics locations. University of California, San Francisco While significant progress in recent years has led to San Francisco, California 94143 a greater understanding of the factors that help establish 3 Departments of Pathology, Anatomy, a topographic map within the retina and its targets and Cell Biology (O’Leary et al., 1999), less progress has been made in Center for Neurobiology and Behavior identifying the rudimentary axon guidance cues that es- Columbia University College of Physicians tablish the basic trajectories within the vertebrate visual and Surgeons system, particularly those that function at the midline New York, New York 10032 to regulate the positioning and decussation of retinal 4 Department of Molecular and Cell Biology axons. In mammals, chondroitin sulfate proteoglycans Howard Hughes Medical Institute (CSPGs), L1, netrin-1, and specific EphB ligands are University of California, Berkeley important for guidance within the retina (Birgbauer et Berkeley, California 94720 al., 2000; Brittis et al., 1992, 1995; Deiner et al., 1997; Snow et al., 1991). -
Supplementary Table 1: Adhesion Genes Data Set
Supplementary Table 1: Adhesion genes data set PROBE Entrez Gene ID Celera Gene ID Gene_Symbol Gene_Name 160832 1 hCG201364.3 A1BG alpha-1-B glycoprotein 223658 1 hCG201364.3 A1BG alpha-1-B glycoprotein 212988 102 hCG40040.3 ADAM10 ADAM metallopeptidase domain 10 133411 4185 hCG28232.2 ADAM11 ADAM metallopeptidase domain 11 110695 8038 hCG40937.4 ADAM12 ADAM metallopeptidase domain 12 (meltrin alpha) 195222 8038 hCG40937.4 ADAM12 ADAM metallopeptidase domain 12 (meltrin alpha) 165344 8751 hCG20021.3 ADAM15 ADAM metallopeptidase domain 15 (metargidin) 189065 6868 null ADAM17 ADAM metallopeptidase domain 17 (tumor necrosis factor, alpha, converting enzyme) 108119 8728 hCG15398.4 ADAM19 ADAM metallopeptidase domain 19 (meltrin beta) 117763 8748 hCG20675.3 ADAM20 ADAM metallopeptidase domain 20 126448 8747 hCG1785634.2 ADAM21 ADAM metallopeptidase domain 21 208981 8747 hCG1785634.2|hCG2042897 ADAM21 ADAM metallopeptidase domain 21 180903 53616 hCG17212.4 ADAM22 ADAM metallopeptidase domain 22 177272 8745 hCG1811623.1 ADAM23 ADAM metallopeptidase domain 23 102384 10863 hCG1818505.1 ADAM28 ADAM metallopeptidase domain 28 119968 11086 hCG1786734.2 ADAM29 ADAM metallopeptidase domain 29 205542 11085 hCG1997196.1 ADAM30 ADAM metallopeptidase domain 30 148417 80332 hCG39255.4 ADAM33 ADAM metallopeptidase domain 33 140492 8756 hCG1789002.2 ADAM7 ADAM metallopeptidase domain 7 122603 101 hCG1816947.1 ADAM8 ADAM metallopeptidase domain 8 183965 8754 hCG1996391 ADAM9 ADAM metallopeptidase domain 9 (meltrin gamma) 129974 27299 hCG15447.3 ADAMDEC1 ADAM-like, -
Slit Proteins: Molecular Guidance Cues for Cells Ranging from Neurons to Leukocytes Kit Wong, Hwan Tae Park*, Jane Y Wu* and Yi Rao†
583 Slit proteins: molecular guidance cues for cells ranging from neurons to leukocytes Kit Wong, Hwan Tae Park*, Jane Y Wu* and Yi Rao† Recent studies of molecular guidance cues including the Slit midline glial cells was thought to be abnormal [2,3]. family of secreted proteins have provided new insights into the Projection of the commissural axons was also abnormal: mechanisms of cell migration. Initially discovered in the nervous instead of crossing the midline once before projecting system, Slit functions through its receptor, Roundabout, and an longitudinally, the commissural axons from two sides of the intracellular signal transduction pathway that includes the nerve cord are fused at the midline in slit mutants [2,3]. Abelson kinase, the Enabled protein, GTPase activating proteins Because the midline glial cells are known to be important and the Rho family of small GTPases. Interestingly, Slit also in axon guidance, the commissural axon phenotype in slit appears to use Roundabout to control leukocyte chemotaxis, mutants was initially thought to be secondary to the cell- which occurs in contexts different from neuronal migration, differentiation phenotype [3]. suggesting a fundamental conservation of mechanisms guiding the migration of distinct types of somatic cells. In early 1999, results from three groups demonstrated independently that Slit functioned as an extracellular cue Addresses to guide axon pathfinding [4–6], to promote axon branching Department of Anatomy and Neurobiology, and *Departments of [7], and to control neuronal migration [8]. The functional Pediatrics and Molecular Biology and Pharmacology, Box 8108, roles of Slit in axon guidance and neuronal migration were Washington University School of Medicine, 660 S Euclid Avenue St Louis, soon supported by other studies in Drosophila [9] and in Missouri 63110, USA *e-mail: [email protected] vertebrates [10–14]. -
Cellular-Resolution Gene Expression Profiling in the Neonatal Marmoset Brain Reveals Dynamic Species- and Region-Specific Differences
Cellular-resolution gene expression profiling in the neonatal marmoset brain reveals dynamic species- and region-specific differences Yoshiaki Kitaa, Hirozumi Nishibea, Yan Wanga, Tsutomu Hashikawaa, Satomi S. Kikuchia, Mami Ua, Aya C. Yoshidaa, Chihiro Yoshidaa, Takashi Kawaseb, Shin Ishiib, Henrik Skibbec, and Tomomi Shimogoria,1 aLaboratory for Molecular Mechanisms of Brain Development, Center for Brain Science, RIKEN, Saitama 351-0198, Japan; bIntegrated Systems Biology Laboratory, Department of Systems Science, Graduate School of Informatics, Kyoto University, Kyoto 606-8501, Japan; and cBrain Image Analysis Unit, Center for Brain Science, RIKEN, Saitama 351-0198, Japan Edited by Edward M. Callaway, Salk Institute for Biological Studies, La Jolla, CA, and approved March 12, 2021 (received for review September 25, 2020) Precise spatiotemporal control of gene expression in the develop- (12). However, these studies are highly resource intensive, re- ing brain is critical for neural circuit formation, and comprehensive quiring substantial time and cost. Consequently, such efforts expression mapping in the developing primate brain is crucial to have been limited, focusing on a few brain regions in limited species understand brain function in health and disease. Here, we devel- (13). Thus, interspecific comparison of brain-cell heterogeneity has oped an unbiased, automated, large-scale, cellular-resolution in situ not been possible. hybridization (ISH)–based gene expression profiling system (GePS) Here, we describe the development and implementation of an and companion analysis to reveal gene expression patterns in the unbiased gene expression profiling system (GePS) for use with neonatal New World marmoset cortex, thalamus, and striatum the Marmoset Gene Atlas (MGA) (https://gene-atlas.brainminds. -
A Concise Review of Human Brain Methylome During Aging and Neurodegenerative Diseases
BMB Rep. 2019; 52(10): 577-588 BMB www.bmbreports.org Reports Invited Mini Review A concise review of human brain methylome during aging and neurodegenerative diseases Renuka Prasad G & Eek-hoon Jho* Department of Life Science, University of Seoul, Seoul 02504, Korea DNA methylation at CpG sites is an essential epigenetic mark position of carbon in the cytosine within CG dinucleotides that regulates gene expression during mammalian development with resultant formation of 5mC. The symmetrical CG and diseases. Methylome refers to the entire set of methylation dinucleotides are also called as CpG, due to the presence of modifications present in the whole genome. Over the last phosphodiester bond between cytosine and guanine. The several years, an increasing number of reports on brain DNA human genome contains short lengths of DNA (∼1,000 bp) in methylome reported the association between aberrant which CpG is commonly located (∼1 per 10 bp) in methylation and the abnormalities in the expression of critical unmethylated form and referred as CpG islands; they genes known to have critical roles during aging and neuro- commonly overlap with the transcription start sites (TSSs) of degenerative diseases. Consequently, the role of methylation genes. In human DNA, 5mC is present in approximately 1.5% in understanding neurodegenerative diseases has been under of the whole genome and CpG base pairs are 5-fold enriched focus. This review outlines the current knowledge of the human in CpG islands than other regions of the genome (3, 4). CpG brain DNA methylomes during aging and neurodegenerative islands have the following salient features. In the human diseases. -
Supplementary Information – Postema Et Al., the Genetics of Situs Inversus Totalis Without Primary Ciliary Dyskinesia
1 Supplementary information – Postema et al., The genetics of situs inversus totalis without primary ciliary dyskinesia Table of Contents: Supplementary Methods 2 Supplementary Results 5 Supplementary References 6 Supplementary Tables and Figures Table S1. Subject characteristics 9 Table S2. Inbreeding coefficients per subject 10 Figure S1. Multidimensional scaling to capture overall genomic diversity 11 among the 30 study samples Table S3. Significantly enriched gene-sets under a recessive mutation model 12 Table S4. Broader list of candidate genes, and the sources that led to their 13 inclusion Table S5. Potential recessive and X-linked mutations in the unsolved cases 15 Table S6. Potential mutations in the unsolved cases, dominant model 22 2 1.0 Supplementary Methods 1.1 Participants Fifteen people with radiologically documented SIT, including nine without PCD and six with Kartagener syndrome, and 15 healthy controls matched for age, sex, education and handedness, were recruited from Ghent University Hospital and Middelheim Hospital Antwerp. Details about the recruitment and selection procedure have been described elsewhere (1). Briefly, among the 15 people with radiologically documented SIT, those who had symptoms reminiscent of PCD, or who were formally diagnosed with PCD according to their medical record, were categorized as having Kartagener syndrome. Those who had no reported symptoms or formal diagnosis of PCD were assigned to the non-PCD SIT group. Handedness was assessed using the Edinburgh Handedness Inventory (EHI) (2). Tables 1 and S1 give overviews of the participants and their characteristics. Note that one non-PCD SIT subject reported being forced to switch from left- to right-handedness in childhood, in which case five out of nine of the non-PCD SIT cases are naturally left-handed (Table 1, Table S1). -
Specific Expression and Methylation of SLIT1, SLIT2, SLIT3, and Mir‑218
INTERNATIONAL JOURNAL OF ONCOLOGY 48: 2497-2507, 2016 Specific expression and methylation ofSLIT1 , SLIT2, SLIT3, and miR‑218 in gastric cancer subtypes MIRANG KIM1,2, JONG-HWAN KIM1,2, SU-JIN BAEK1,2, SEON-YOUNG KIM1,2 and YONG SUNG KIM1,2 1Genome Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB); 2Department of Functional Genomics, University of Science and Technology, Daejeon 34141, Republic of Korea Received December 20, 2015; Accepted January 27, 2016 DOI: 10.3892/ijo.2016.3473 Abstract. SLIT has been suggested as a key regulator of microsatellite instability (MSI), genomically stable (GS), and cancer development and a promising therapeutic target for chromosomal instability (CIN) (2). Nearly 9% of gastric cancer treatment. Herein, we analyzed expression and meth- cancer is EBV-positive (3), for which methylation of tumor ylation of SLIT1/SLIT2/SLIT3 in 11 gastric cancer cell lines, suppressor genes is a key abnormality (4). MSI is a common 96 paired gastric tumors and adjacent normal gastric tissues, feature of gastric cancers that occurs in 15-30% of cases (5). and 250 gastric cancers provided by The Cancer Genome DNA mismatch repair deficiency such as methylation of the Atlas. Methylation of SLIT1/SLIT2/SLIT3 was found both in MLH1 promoter increases the frequency of mutations across early gastric cancers, and in advanced gastric cancers. Even the genome, creating MSI (5). Not only MLH1 but also many normal gastric tissue showed increased methylation of SLIT1 other tumor suppressor genes are frequently hypermethylated and SLIT3 that correlated with patient age. Furthermore, in MSI-positive gastric cancer (6). -
Conserved Modularity and Potential for Alternate Splicing in Mouse and Human Slit Genes
Int. J. Dev. Biol. 46: 385-391 (2002) Conserved modularity and potential for alternate splicing in mouse and human Slit genes MELISSA LITTLE*, BREE RUMBALLE1, KYLIE GEORGAS, TOSHIYA YAMADA and ROHAN D. TEASDALE Institute for Molecular Bioscience and Centre for Functional and Applied Genomics, University of Queensland, St. Lucia, Australia and 1Department of Biochemistry, University of Queensland, St. Lucia, Australia ABSTRACT The vertebrate Slit gene family currently consists of three members; Slit1, Slit2 and Slit3. Each gene encodes a protein containing multiple epidermal growth factor and leucine rich repeat motifs, which are likely to have importance in cell-cell interactions. In this study, we sought to fully define and characterise the vertebrate Slit gene family. Using long distance PCR coupled with in silico mapping, we determined the genomic structure of all three Slit genes in mouse and man. Analysis of EST and genomic databases revealed no evidence of further Slit family members in either organism. All three Slit genes were encoded by 36 (Slit3) or 37 (Slit1 and Slit2) exons covering at least 143 kb or 183 kb of mouse or human genomic DNA respectively. Two additional potential leucine-rich repeat encoding exons were identified within intron 12 of Slit2. These could be inserted in frame, suggesting that alternate splicing may occur in Slit2. A search for STS sequences within human Slit3 anchored this gene to D5S2075 at the 5’ end (exon 4) and SGC32449 within the 3’ UTR, suggesting that Slit3 may cover greater than 693 kb. The genomic structure of all Slit genes demonstrated considerable modularity in the placement of exon-intron boundaries such that individual leucine-rich repeat motifs were encoded by individual 72 bp exons. -
Cholesterol 25-Hydroxylase on Chromosome 10Q Is a Susceptibility Gene for Sporadic Alzheimer’S Disease
Zurich Open Repository and Archive University of Zurich Main Library Strickhofstrasse 39 CH-8057 Zurich www.zora.uzh.ch Year: 2005 Cholesterol 25-hydroxylase on chromosome 10q is a susceptibility gene for sporadic Alzheimer’s disease Papassotiropoulos, A ; Lambert, J C ; Wavrant-De Vrièze, F ; Wollmer, M A ; von der Kammer, H ; Streffer, J R ; Maddalena, A ; Huynh, K D ; Wolleb, S ; Lütjohann, D ; Schneider, B;Thal,DR Grimaldi, L M E ; Tsolaki, M ; Kapaki, E ; Ravid, R ; Konietzko, U ; Hegi, T ; Pasch, T ; Jung, H ; Braak, H ; Amouyel, P ; Rogaev, E I ; Hardy, J ; Hock, C ; Nitsch, R M Abstract: Alzheimer’s disease (AD) is the most common cause of dementia. It is characterized by beta- amyloid (A beta) plaques, neurofibrillary tangles and the degeneration of specifically vulnerable brain neurons. We observed high expression of the cholesterol 25-hydroxylase (CH25H) gene in specifically vulnerable brain regions of AD patients. CH25H maps to a region within 10q23 that has been previ- ously linked to sporadic AD. Sequencing of the 5’ region of CH25H revealed three common haplotypes, CH25Hchi2, CH25Hchi3 and CH25Hchi4; CSF levels of the cholesterol precursor lathosterol were higher in carriers of the CH25Hchi4 haplotype. In 1,282 patients with AD and 1,312 healthy control subjects from five independent populations, a common variation in the vicinity of CH25H was significantly associated with the risk for sporadic AD (p = 0.006). Quantitative neuropathology of brains from elderly non- demented subjects showed brain A beta deposits in carriers of CH25Hchi4 and CH25Hchi3 haplotypes, whereas no A beta deposits were present in CH25Hchi2 carriers. -
A Concise Review of Human Brain Methylome During Aging and Neurodegenerative Diseases
BMB Rep. 2019; 52(10): 577-588 BMB www.bmbreports.org Reports Invited Mini Review A concise review of human brain methylome during aging and neurodegenerative diseases Renuka Prasad G & Eek-hoon Jho* Department of Life Science, University of Seoul, Seoul 02504, Korea DNA methylation at CpG sites is an essential epigenetic mark position of carbon in the cytosine within CG dinucleotides that regulates gene expression during mammalian development with resultant formation of 5mC. The symmetrical CG and diseases. Methylome refers to the entire set of methylation dinucleotides are also called as CpG, due to the presence of modifications present in the whole genome. Over the last phosphodiester bond between cytosine and guanine. The several years, an increasing number of reports on brain DNA human genome contains short lengths of DNA (∼1,000 bp) in methylome reported the association between aberrant which CpG is commonly located (∼1 per 10 bp) in methylation and the abnormalities in the expression of critical unmethylated form and referred as CpG islands; they genes known to have critical roles during aging and neuro- commonly overlap with the transcription start sites (TSSs) of degenerative diseases. Consequently, the role of methylation genes. In human DNA, 5mC is present in approximately 1.5% in understanding neurodegenerative diseases has been under of the whole genome and CpG base pairs are 5-fold enriched focus. This review outlines the current knowledge of the human in CpG islands than other regions of the genome (3, 4). CpG brain DNA methylomes during aging and neurodegenerative islands have the following salient features. In the human diseases. -
Results to Test Classic Anthropological Hypotheses: Human Third Molar Agenesis and the ‘Probable Mutation Effect’ Alexis Sullivan [email protected]
Wayne State University Human Biology Open Access Pre-Prints WSU Press 9-1-2016 Extending genome-wide association study (GWAS) results to test classic anthropological hypotheses: Human third molar agenesis and the ‘probable mutation effect’ Alexis Sullivan [email protected] Adrijana Vukelic [email protected] Jacob Cohen [email protected] George (PJ) Perry Pennsylvania State University, [email protected] Recommended Citation Sullivan, Alexis; Vukelic, Adrijana; Cohen, Jacob; and Perry, George (PJ), "Extending genome-wide association study (GWAS) results to test classic anthropological hypotheses: Human third molar agenesis and the ‘probable mutation effect’" (2016). Human Biology Open Access Pre-Prints. 116. http://digitalcommons.wayne.edu/humbiol_preprints/116 This Open Access Preprint is brought to you for free and open access by the WSU Press at DigitalCommons@WayneState. It has been accepted for inclusion in Human Biology Open Access Pre-Prints by an authorized administrator of DigitalCommons@WayneState. Invited Commentary Extending genome-wide association study (GWAS) results to test classic anthropological hypotheses: Human third molar agenesis and the ‘probable mutation effect’ Adrijana Vukelic1,2, Jacob A. Cohen2, Alexis P. Sullivan2, George H. Perry1,2 1 Department of Anthropology, Pennsylvania State University, University Park, PA 16802 2 Department of Biology, Pennsylvania State University, University Park, PA 16802 Date Submitted: May 10 2016 Date Accepted: Feb 24 2017 Running title: Human M3 agenesis evolutionary genetics Keywords: Anthropometric traits; evolutionary genomics; Human dental formula evolution; wisdom tooth Corresponding author: George H. Perry 513 Carpenter Building Pennsylvania State University University Park, PA 16802 USA E-mail: [email protected] Phone: +1-814-863-7654 Pre-print version.