A HERV-K provirus in chimpanzees, bonobos and gorillas, but not humans

Slides:



Advertisements
Similar presentations
HA Hong-seok, HUH Jae-Won, KIM Dae-Soo 1, JOO Myung-Jin 2 and KIM Heui-Soo* Division of Biological Sciences, College of Natural Sciences, Pusan National.
Advertisements

Recurrent inversion breaking intron 1 of the factor VIII gene is a frequent cause of severe hemophilia A by Richard D. Bagnall, Naushin Waseem, Peter M.
Volume 7, Issue 6, Pages (December 1997)
RHD gene deletion occurred in the Rhesus box
The Mre11 Complex Is Required for Repair of Hairpin-Capped Double-Strand Breaks and Prevention of Chromosome Rearrangements  Kirill S. Lobachev, Dmitry.
Betaine, Dimethyl Sulfoxide, and 7-Deaza-dGTP, a Powerful Mixture for Amplification of GC-Rich DNA Sequences  Marco Musso, Renata Bocciardi, Sara Parodi,
Volume 38, Issue 4, Pages (May 2010)
Polymorphisms in the H19 Gene and the Risk of Bladder Cancer
Base-Pairing between Untranslated Regions Facilitates Translation of Uncapped, Nonpolyadenylated Viral RNA  Liang Guo, Edwards M. Allen, W.Allen Miller 
Volume 16, Issue 9, Pages (May 2006)
Volume 17, Issue 8, Pages (April 2007)
Volume 19, Issue 4, Pages (October 2003)
Reciprocal Crossovers and a Positional Preference for Strand Exchange in Recombination Events Resulting in Deletion or Duplication of Chromosome 17p11.2 
Transient Gene Expression by Nonintegrating Lentiviral Vectors
Recombination between Palindromes P5 and P1 on the Human Y Chromosome Causes Massive Deletions and Spermatogenic Failure  Sjoerd Repping, Helen Skaletsky,
Volume 146, Issue 6, Pages (September 2011)
High-Resolution Mapping of Crossovers in Human Sperm Defines a Minisatellite- Associated Recombination Hotspot  Alec J Jeffreys, John Murray, Rita Neumann 
Evolution of natural killer cell receptors
ATLAS: A System to Selectively Identify Human-Specific L1 Insertions
Volume 45, Issue 3, Pages (February 2012)
Volume 3, Issue 4, Pages (April 2013)
Catherine E. Keegan, Anthony A. Killeen 
Human Epidermal Differentiation Complex in a Single 2
Myotonic Dystrophy Type 2: Human Founder Haplotype and Evolutionary Conservation of the Repeat Tract  Christina L. Liquori, Yoshio Ikeda, Marcy Weatherspoon,
Size Polymorphisms in the Human Ultrahigh Sulfur Hair Keratin-Associated Protein 4, KAP4, Gene Family  Naoyuki Kariya, Yutaka Shimomura, Masaaki Ito 
Patching Broken Chromosomes with Extranuclear Cellular DNA
Supplemental Figure 3 A B C T-DNA 1 2 RGLG1 2329bp 3 T-DNA 1 2 RGLG2
Structural Analysis of Insulin Minisatellite Alleles Reveals Unusually Large Differences in Diversity between Africans and Non-Africans  John D.H. Stead,
Structure of the GM2A Gene: Identification of an Exon 2 Nonsense Mutation and a Naturally Occurring Transcript with an In-Frame Deletion of Exon 2  Biao.
Lauren M. Mathews, Susan Y
Volume 11, Issue 12, Pages (June 2001)
Yeast Origins Establish a Strand Bias for Replicational Mutagenesis
DNA Transposition by the RAG1 and RAG2 Proteins
Rare Sequence Variation in the Genome Flanking a Short Tandem Repeat Locus Can Lead to a Question of “Nonmaternity”  Anne Deucher, Tsoyu Chiang, Iris.
A Multi-Exonic BRCA1 Deletion Identified in Multiple Families through Single Nucleotide Polymorphism Haplotype Pair Analysis and Gene Amplification with.
Comparison of the variable regions of (A) pHNZY32, pHNZY118, and pHNAH24; (B) pHNMCC14; (C) pHNFKU92; (D) pE80; (E) pECB11; (F) p42-2; and (G) pSLK172-2.
Volume 138, Issue 7, Pages (June 2010)
X-Linked Congenital Hypertrichosis Syndrome Is Associated with Interchromosomal Insertions Mediated by a Human-Specific Palindrome near SOX3  Hongwen.
The Divergent U12-Type Spliceosome Is Required for Pre-mRNA Splicing and Is Essential for Development in Drosophila  Leo R. Otake, Petra Scamborova, Carl.
Human Genomic Deletions Mediated by Recombination between Alu Elements
A Comprehensive Analysis of Recently Integrated Human Ta L1 Elements
Beth Elliott, Christine Richardson, Maria Jasin  Molecular Cell 
Karmella A. Haynes, Amy A. Caudy, Lynne Collins, Sarah C.R. Elgin 
A DNA Replication Mechanism for Generating Nonrecurrent Rearrangements Associated with Genomic Disorders  Jennifer A. Lee, Claudia M.B. Carvalho, James.
Michael A. Rogers, Hermelita Winter, Christian Wolf, Jürgen Schweizer 
Reciprocal Crossovers and a Positional Preference for Strand Exchange in Recombination Events Resulting in Deletion or Duplication of Chromosome 17p11.2 
A modest but significant effect of CGB5 gene promoter polymorphisms in modulating the risk of recurrent miscarriage  Kristiina Rull, M.D., Ph.D., Ole.
Sex-Linked period Genes in the Silkmoth, Antheraea pernyi
Complete Haplotype Sequence of the Human Immunoglobulin Heavy-Chain Variable, Diversity, and Joining Genes and Characterization of Allelic and Copy-Number.
Volume 6, Issue 7, Pages (July 1996)
Gene Density, Transcription, and Insulators Contribute to the Partition of the Drosophila Genome into Physical Domains  Chunhui Hou, Li Li, Zhaohui S.
Evolutionary History of the ADRB2 Gene in Humans
Template Switching by RNA Polymerase II In Vivo
Volume 6, Issue 4, Pages (July 2013)
Neanderthal and Denisovan retroviruses in modern humans
Volume 17, Issue 5, Pages (May 2009)
Volume 16, Issue 4, Pages (April 2002)
Sugar Receptors in Drosophila
Jingwei Ni, Amy L Tien, Maurille J Fournier  Cell 
Promoting in Tandem: The Promoter for Telomere Transposon HeT-A and Implications for the Evolution of Retroviral LTRs  O.N Danilevskaya, I.R Arkhipova,
Identification of TSIX, Encoding an RNA Antisense to Human XIST, Reveals Differences from its Murine Counterpart: Implications for X Inactivation  Barbara.
MicroRNA Binding Sites in Arabidopsis Class III HD-ZIP mRNAs Are Required for Methylation of the Template Chromosome  Ning Bao, Khar-Wai Lye, M.Kathryn.
Volume 21, Issue 23, Pages (December 2011)
Mutation of the Ca2+ Channel β Subunit Gene Cchb4 Is Associated with Ataxia and Seizures in the Lethargic (lh) Mouse  Daniel L Burgess, Julie M Jones,
Volume 9, Issue 16, Pages S1-868 (August 1999)
Rodney A King, Sarbani Banik-Maiti, Ding Jun Jin, Robert A Weisberg 
Molecular Characterization of the Pericentric Inversion That Causes Differences Between Chimpanzee Chromosome 19 and Human Chromosome 17  Hildegard Kehrer-Sawatzki,
Exon Skipping in IVD RNA Processing in Isovaleric Acidemia Caused by Point Mutations in the Coding Region of the IVD Gene  Jerry Vockley, Peter K. Rogan,
CRISPR Immunological Memory Requires a Host Factor for Specificity
Meiotic DNA Breaks at the S. pombe Recombination Hot Spot M26
Presentation transcript:

A HERV-K provirus in chimpanzees, bonobos and gorillas, but not humans Madalina Barbulescu, Geoffrey Turner, Mei Su, Rachel Kim, Michael I Jensen-Seaman, Amos S Deinard, Kenneth K Kidd, Jack Lenz  Current Biology  Volume 11, Issue 10, Pages 779-783 (May 2001) DOI: 10.1016/S0960-9822(01)00227-5

Figure 1 PCR amplification of HERV-K-GC1 from primate genomic DNAs. Species abbreviations are: M.m., Macaca mulatta; P.py., Pongo pygmaeus; G.g., Gorilla gorilla; P.pa., Pan paniscus; P.t., Pan troglodytes; and H.s., Homo sapiens. (a) A map of the HERV-K-GC1 preintegration and proviral loci. Arrows show the positions of PCR primers used in this study. Primers within HERV-K were from Barbulescu et al. [14]. Those from the flanking sequences were based on the human sequence from BAC RPCI11–500M8 (GenBank Accession number AC005832). Macaca mulatta lacks a stretch of about 600 bp relative to the hominoid species near primer 3′f. The white boxes indicate the 5 bp target sequence that was duplicated during the integration of HERV-K-GC1. The black rectangles denote the HERV-K long terminal repeats (LTRs). (b) PCR amplification of the provirus junctions and preintegration site. Each lane shows the products from a different individual of the indicated species. M, marker. (c) PCR amplification of the HERV-K-GC1 provirus and preintegration site using different primer pairs in one individual of each of the indicated species Current Biology 2001 11, 779-783DOI: (10.1016/S0960-9822(01)00227-5)

Figure 2 Sequences flanking the HERV-K-GC1 insertion site in different primate species. Sequences were entered into GenBank (Accession numbers AF294259-AF294264). (a) A diagram showing the sequenced region relative to the position of the provirus in Gorilla and Pan. The numbers to the left of each line show the differences between the corresponding sequence and the human sequence, in which each substitution, insertion, or deletion relative to human was counted as one difference. The black rectangles indicate the HERV-K long terminal repeats (LTRs). The white boxes indicate the 5 bp (ATTAT) that were duplicated flanking the provirus in Gorilla and Pan. These are present only once in Homo, Pongo, and Macaca. The 5 bp sequence is present at nucleotide 173,033 of version AC005832.1 of the BAC. GENSCAN 1.0 analysis of the human BAC predicted the presence of a gene similar to one of unknown function predicted within the Drosophila melanogaster genome (CG9986, GenBank Accession numbers AAF56802) ∼2 kb downstream of the position of the provirus in Gorilla and Pan and in the opposite transcriptional orientation. RepeatMasker analysis of the human BAC indicated that there were several L1 sequences and an Alu element within a 5 kbp stretch surrounding the provirus insertion site in apes. (b) The sequences corresponding to 165 bp flanking either side of the provirus. Asterisks indicate the positions of single base pair substitutions. Deletions in the indicated species are shown as gaps. (c) Sequences of 40 bp immediately flanking either side of the provirus. Dots indicate sequence identity relative to the human sequence. Dashes indicate the absence of the corresponding nucleotide. The last five nucleotides of the viral LTRs are shown in the black rectangles. (d) Segregation of the empty preintegration allele (E) and the provirus allele (V) in the Homo, Pan, and Gorilla lineages. E + V indicates that both alleles were present in the population of the cognate species. LCA, last common ancestor Current Biology 2001 11, 779-783DOI: (10.1016/S0960-9822(01)00227-5)