Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
1995-9-7
pubmed:databankReference
pubmed:abstractText
Using gene targeting in embryonic stem cells, we have derived mice with a null mutation in a DNA mismatch repair gene homolog, PMS2. We observed microsatellite instability in the male germline, in tail, and in tumor DNA of PMS2-deficient animals. We therefore conclude that PMS2 is involved in DNA mismatch repair in a variety of tissues. PMS2-deficient animals appear prone to sarcomas and lymphomas. PMS2-deficient males are infertile, producing only abnormal spermatozoa. Analysis of axial element and synaptonemal complex formation during prophase of meiosis I indicates abnormalities in chromosome synapsis. These observations suggest links among mismatch repair, genetic recombination, and chromosome synapsis in meiosis.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0092-8674
pubmed:author
pubmed:issnType
Print
pubmed:day
28
pubmed:volume
82
pubmed:geneSymbol
PMS2
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
309-19
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed-meshheading:7628019-Adenosine Triphosphatases, pubmed-meshheading:7628019-Alleles, pubmed-meshheading:7628019-Amino Acid Sequence, pubmed-meshheading:7628019-Animals, pubmed-meshheading:7628019-Base Composition, pubmed-meshheading:7628019-Base Sequence, pubmed-meshheading:7628019-Chromosome Aberrations, pubmed-meshheading:7628019-Chromosome Disorders, pubmed-meshheading:7628019-Cloning, Molecular, pubmed-meshheading:7628019-DNA, pubmed-meshheading:7628019-DNA Primers, pubmed-meshheading:7628019-DNA Repair, pubmed-meshheading:7628019-DNA Repair Enzymes, pubmed-meshheading:7628019-DNA-Binding Proteins, pubmed-meshheading:7628019-Embryo, Mammalian, pubmed-meshheading:7628019-Female, pubmed-meshheading:7628019-Genetic Predisposition to Disease, pubmed-meshheading:7628019-Genotype, pubmed-meshheading:7628019-Humans, pubmed-meshheading:7628019-Lymphoma, pubmed-meshheading:7628019-Male, pubmed-meshheading:7628019-Meiosis, pubmed-meshheading:7628019-Mice, pubmed-meshheading:7628019-Mice, Mutant Strains, pubmed-meshheading:7628019-Molecular Sequence Data, pubmed-meshheading:7628019-Oligodeoxyribonucleotides, pubmed-meshheading:7628019-Polymerase Chain Reaction, pubmed-meshheading:7628019-Protein Biosynthesis, pubmed-meshheading:7628019-Proteins, pubmed-meshheading:7628019-Recombinant Proteins, pubmed-meshheading:7628019-Restriction Mapping, pubmed-meshheading:7628019-Sarcoma, pubmed-meshheading:7628019-Seminiferous Tubules, pubmed-meshheading:7628019-Sequence Homology, Amino Acid, pubmed-meshheading:7628019-Spermatocytes, pubmed-meshheading:7628019-Spermatozoa
pubmed:year
1995
pubmed:articleTitle
Male mice defective in the DNA mismatch repair gene PMS2 exhibit abnormal chromosome synapsis in meiosis.
pubmed:affiliation
Department of Molecular and Medical Genetics, Oregon Health Sciences University, Portland 97201-3098, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't