Regulation of meiotic chromatin loop size by chromosomal position.

PubWeight™: 1.04‹?› | Rank: Top 15%

🔗 View Article (PMC 39712)

Published in Proc Natl Acad Sci U S A on April 02, 1996

Authors

H H Heng1, J W Chamberlain, X M Shi, B Spyropoulos, L C Tsui, P B Moens

Author Affiliations

1: Department of Biology, York University, Downsview, ON Canada.

Articles citing this

Centromere and telomere movements during early meiotic prophase of mouse and man are associated with the onset of chromosome pairing. J Cell Biol (1996) 2.88

A specificity and targeting subunit of a human SWI/SNF family-related chromatin-remodeling complex. Mol Cell Biol (2000) 2.70

Mammalian recombination hot spots: properties, control and evolution. Nat Rev Genet (2010) 2.54

Polymer models of meiotic and mitotic chromosomes. Mol Biol Cell (1997) 1.57

Mammalian meiotic telomeres: protein composition and redistribution in relation to nuclear pores. Mol Biol Cell (2000) 1.39

Telomere attachment, meiotic chromosome condensation, pairing, and bouquet stage duration are modified in spermatocytes lacking axial elements. Mol Biol Cell (2003) 1.26

Meiotic cohesins modulate chromosome compaction during meiotic prophase in fission yeast. J Cell Biol (2006) 1.25

Condensin I reveals new insights on mouse meiotic chromosome structure and dynamics. PLoS One (2007) 0.95

Nucleotide excision repair in rat male germ cells: low level of repair in intact cells contrasts with high dual incision activity in vitro. Nucleic Acids Res (2001) 0.95

Extreme axial equalization and wide distribution of recombination nodules in the primitive ZW pair of Rhea americana (Aves, Ratitae). Chromosome Res (1997) 0.93

Characterization of telomere-subtelomere junctions in Silene latifolia. Mol Genet Genomics (2003) 0.83

Imaging genome abnormalities in cancer research. Cell Chromosome (2004) 0.80

Dynamic relocation of telomere complexes in mouse meiotic chromosomes. Chromosome Res (2003) 0.79

Physical origin of the contact frequency in chromosome conformation capture data. Biophys J (2013) 0.78

Many functions of the meiotic cohesin. Chromosome Res (2010) 0.78

Defective imprint resetting in carriers of Robertsonian translocation Rb (8.12). Mamm Genome (2010) 0.78

Dynamics of response to asynapsis and meiotic silencing in spermatocytes from Robertsonian translocation carriers. PLoS One (2013) 0.77

Chromatin organization and remodeling of interstitial telomeric sites during meiosis in the Mongolian gerbil (Meriones unguiculatus). Genetics (2014) 0.75

Organization of repetitive DNA sequences at pachytene chromosomes of gilthead seabream Sparus aurata (Pisces, Perciformes). Chromosome Res (2000) 0.75

Articles cited by this

The structure of histone-depleted metaphase chromosomes. Cell (1977) 6.78

Hypervariable ultra-long telomeres in mice. Nature (1990) 4.76

Synaptonemal complex proteins: occurrence, epitope mapping and chromosome disjunction. J Cell Sci (1994) 3.21

Telomere-proximal DNA in Saccharomyces cerevisiae is refractory to methyltransferase activity in vivo. Proc Natl Acad Sci U S A (1992) 2.80

High-resolution mapping of mammalian genes by in situ hybridization to free chromatin. Proc Natl Acad Sci U S A (1992) 2.72

Modes of DAPI banding and simultaneous in situ hybridization. Chromosoma (1993) 2.38

Telomeres: no end in sight. Cell (1994) 2.31

Unusual chromatin in human telomeres. Mol Cell Biol (1994) 2.19

Two simple procedures for releasing chromatin from routinely fixed cells for fluorescence in situ hybridization. Cytogenet Cell Genet (1994) 1.61

Nucleosomal organization of telomere-specific chromatin in rat. Cell (1993) 1.33

Differentiation of the synaptonemal complex and the kinetochore in Locusta spermatocytes studied by whole mount electron microscopy. Chromosoma (1973) 1.24

Computer measurements and graphics of three-dimensional cellular ultrastructure. J Ultrastruct Res (1981) 1.19

Tissue-specific and cell surface expression of human major histocompatibility complex class I heavy (HLA-B7) and light (beta 2-microglobulin) chain genes in transgenic mice. Proc Natl Acad Sci U S A (1988) 1.15

Telomere and centromere DNA are associated with the cores of meiotic prophase chromosomes. Chromosoma (1990) 1.04

Mammalian meiotic recombination: a reexamination. Hum Genet (1994) 1.02

Satellite DNA I in chromatin loops of rat pachytene chromosomes and in spermatids. Chromosoma (1989) 0.97

Organization of heterologous DNA inserts on the mouse meiotic chromosome core. Chromosoma (1994) 0.96

Synaptonemal complexes from DNase-treated rat pachytene chromosomes contain (GT)n and LINE/SINE sequences. Genetics (1992) 0.92

Isolation and preliminary characterization of the synaptonemal complex from rat pachytene spermatocytes. Exp Cell Res (1983) 0.82

Articles by these authors

Identification of the cystic fibrosis gene: genetic analysis. Science (1989) 33.61

Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomas. Nat Genet (1997) 6.83

Cystic fibrosis locus defined by a genetically linked polymorphic DNA marker. Science (1985) 5.81

Spindles, spindle plaques, and meiosis in the yeast Saccharomyces cerevisiae (Hansen). J Cell Biol (1971) 5.79

Mutations in the human Sonic Hedgehog gene cause holoprosencephaly. Nat Genet (1996) 5.70

A cluster of cystic fibrosis mutations in the first nucleotide-binding fold of the cystic fibrosis conductance regulator protein. Nature (1990) 5.42

A polymorphic DNA marker linked to cystic fibrosis is located on chromosome 7. Nature (1985) 5.07

The relation between genotype and phenotype in cystic fibrosis--analysis of the most common mutation (delta F508). N Engl J Med (1990) 4.70

Mutation analysis for heterozygote detection and the prenatal diagnosis of cystic fibrosis. N Engl J Med (1990) 4.60

A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome. Nat Genet (2001) 4.58

Genomic DNA sequence of the cystic fibrosis transmembrane conductance regulator (CFTR) gene. Genomics (1991) 4.27

MADR2 maps to 18q21 and encodes a TGFbeta-regulated MAD-related protein that is functionally mutated in colorectal carcinoma. Cell (1996) 4.13

Correction of the cystic fibrosis defect in vitro by retrovirus-mediated gene transfer. Cell (1990) 3.70

Specific and redundant functions of Gli2 and Gli3 zinc finger genes in skeletal patterning and development. Development (1997) 3.66

Expression of the cystic fibrosis gene in non-epithelial invertebrate cells produces a regulated anion conductance. Cell (1991) 3.56

Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly. Nat Genet (1996) 3.50

Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor. Cell (1997) 3.42

Cystic fibrosis: genotypic and phenotypic variations. Annu Rev Genet (1995) 3.27

Synaptonemal complex proteins: occurrence, epitope mapping and chromosome disjunction. J Cell Sci (1994) 3.21

Multi-ion pore behaviour in the CFTR chloride channel. Nature (1993) 3.14

A suggested nomenclature for designating mutations. Hum Mutat (1993) 3.10

Comparative analysis of the gene-dense ACHE/TFR2 region on human chromosome 7q22 with the orthologous region on mouse chromosome 5. Nucleic Acids Res (2001) 2.89

Plant viral synergism: the potyviral genome encodes a broad-range pathogenicity enhancer that transactivates replication of heterologous viruses. Plant Cell (1997) 2.84

High-resolution mapping of mammalian genes by in situ hybridization to free chromatin. Proc Natl Acad Sci U S A (1992) 2.72

Rapid nonradioactive detection of the major cystic fibrosis mutation. Am J Hum Genet (1990) 2.72

Structure and chromosomal localization of the human constitutive endothelial nitric oxide synthase gene. J Biol Chem (1993) 2.69

Modulation of disease severity in cystic fibrosis transmembrane conductance regulator deficient mice by a secondary genetic factor. Nat Genet (1996) 2.65

A mutation in CFTR produces different phenotypes depending on chromosomal background. Nat Genet (1993) 2.64

Introduction and recovery of a selectable bacterial gene from the genome of mammalian cells. Mol Cell Biol (1982) 2.59

A human gene that shows identity with the gene encoding the angiotensin receptor is located on chromosome 11. Gene (1993) 2.59

Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy. Nat Genet (1998) 2.51

Fine structure of ascospore development in the yeast Saccharomyces cerevisiae. Can J Microbiol (1971) 2.50

Genetic determination of exocrine pancreatic function in cystic fibrosis. Am J Hum Genet (1992) 2.48

Modes of DAPI banding and simultaneous in situ hybridization. Chromosoma (1993) 2.38

Two patients with cystic fibrosis, nonsense mutations in each cystic fibrosis gene, and mild pulmonary disease. N Engl J Med (1990) 2.37

Characterization of the human beta-crystallin gene Hu beta A3/A1 reveals ancestral relationships among the beta gamma-crystallin superfamily. J Biol Chem (1986) 2.31

Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development. Hum Mol Genet (1996) 2.29

Aberrant nuclear behavior at meiosis and anucleate spore formation by sporulation-deficient (SPO) mutants of Saccharomyces cerevisiae. Exp Cell Res (1974) 2.27

Genetic ablation: targeted expression of a toxin gene causes microphthalmia in transgenic mice. Science (1987) 2.27

Permeability of wild-type and mutant cystic fibrosis transmembrane conductance regulator chloride channels to polyatomic anions. J Gen Physiol (1997) 2.26

Molecular characterization of a common fragile site (FRA7H) on human chromosome 7 by the cloning of a simian virus 40 integration site. Proc Natl Acad Sci U S A (1998) 2.16

Identification of mutations in exons 1 through 8 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene. Genomics (1991) 2.07

Meiosis in a temperature-sensitive DNA-synthesis mutant and in an apomictic yeast strain (Saccharomyces cerevisiae). Philos Trans R Soc Lond B Biol Sci (1977) 1.95

Rad51 immunocytology in rat and mouse spermatocytes and oocytes. Chromosoma (1997) 1.90

Methods for analysis of multiple cystic fibrosis mutations. Hum Genet (1991) 1.88

Chromosome number of a small protist: accurate determination. Science (1969) 1.87

The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier protein. Nat Genet (1999) 1.87

Atm deficiency results in severe meiotic disruption as early as leptonema of prophase I. Development (1998) 1.81

RAD51 and DMC1 form mixed complexes associated with mouse meiotic chromosome cores and synaptonemal complexes. J Cell Biol (1999) 1.81

Identification of revertants for the cystic fibrosis delta F508 mutation using STE6-CFTR chimeras in yeast. Cell (1993) 1.72

Correlation of sweat chloride concentration with classes of the cystic fibrosis transmembrane conductance regulator gene mutations. J Pediatr (1995) 1.70

DNA marker haplotype association with pancreatic sufficiency in cystic fibrosis. Am J Hum Genet (1989) 1.66

Synaptonemal complex antigen location and conservation. J Cell Biol (1987) 1.65

Modification of sporulation in yeast strains with two-spored asci (Saccharomyces, Ascomycetes). J Cell Sci (1974) 1.65

Two-dimensional protein patterns during growth and sporulation in Saccharomyces cerevisiae. J Bacteriol (1979) 1.63

Molecular analysis of the PDS gene in Pendred syndrome. Hum Mol Genet (1998) 1.58

CFTR gene variant for patients with congenital absence of vas deferens. Am J Hum Genet (1995) 1.47

Persistence of freely replicating SV40 recombinant molecules carrying a selectable marker in permissive simian cells. Cell (1982) 1.47

An everted repeat mediates retinoic acid induction of the gamma F-crystallin gene: evidence of a direct role for retinoids in lens development. Genes Dev (1993) 1.46

Spindle and kinetochore morphology of Dictyostelium discoideum. J Cell Biol (1976) 1.45

Lung disease in mice with cystic fibrosis. J Clin Invest (1997) 1.44

The fine structure of meiotic chromosome polarization and pairing in Locusta migratoria spermatocytes. Chromosoma (1969) 1.43

Cloning and characterization of PDK4 on 7q21.3 encoding a fourth pyruvate dehydrogenase kinase isoenzyme in human. J Biol Chem (1996) 1.41

Detection of a cystic fibrosis modifier locus for meconium ileus on human chromosome 19q13. Nat Genet (1999) 1.41

PMS2-related genes flank the rearrangement breakpoints associated with Williams syndrome and other diseases on human chromosome 7. Genomics (1997) 1.38

A frameshift mutation in the gamma E-crystallin gene of the Elo mouse. Nat Genet (1992) 1.37

Clinical and genetic comparisons of patients with cystic fibrosis, with or without meconium ileus. J Pediatr (1989) 1.37

Synaptonemal complex proteins. Genome (1989) 1.36

Molecular cytogenetic characterization of a critical region in bands 7q35-q36 commonly deleted in malignant myeloid disorders. Blood (1998) 1.36

Identification of two major components of the lateral elements of synaptonemal complexes of the rat. Eur J Cell Biol (1987) 1.35

Characterization of a novel human SMC heterodimer homologous to the Schizosaccharomyces pombe Rad18/Spr18 complex. Mol Biol Cell (2001) 1.34

Phosphatase inhibitors activate normal and defective CFTR chloride channels. Proc Natl Acad Sci U S A (1994) 1.34

Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patients. Genomics (1996) 1.33

Synaptic structures in the nuclei of sporulating yeast, Saccharomyces cerevisiae (Hansen). J Cell Sci (1971) 1.33

Localization of the gene encoding the alpha 2/delta-subunits of the L-type voltage-dependent calcium channel to chromosome 7q and analysis of the segregation of flanking markers in malignant hyperthermia susceptible families. Hum Mol Genet (1994) 1.32

Genetic analysis of cystic fibrosis using linked DNA markers. Am J Hum Genet (1986) 1.32

Cloning and chromosomal mapping of three novel genes, GPR9, GPR10, and GPR14, encoding receptors related to interleukin 8, neuropeptide Y, and somatostatin receptors. Genomics (1995) 1.32

Human and mouse homologs of Schizosaccharomyces pombe rad1(+) and Saccharomyces cerevisiae RAD17: linkage to checkpoint control and mammalian meiosis. Genes Dev (1998) 1.31

A locus for a human hereditary cataract is closely linked to the gamma-crystallin gene family. Proc Natl Acad Sci U S A (1987) 1.31

Identification of the human cortactin-binding protein-2 gene from the autism candidate region at 7q31. Genomics (2001) 1.30

5' proximal potyviral sequences mediate potato virus X/potyviral synergistic disease in transgenic tobacco. Virology (1995) 1.30

Structural and evolutionary relationships among five members of the human gamma-crystallin gene family. Mol Cell Biol (1985) 1.29

DNA amplification for detection of the XV-2c polymorphism linked to cystic fibrosis. Nucleic Acids Res (1989) 1.29

Involvement of the HLXB9 homeobox gene in Currarino syndrome. Am J Hum Genet (2000) 1.29

Cystic fibrosis transmembrane conductance regulator and obstructive azoospermia. Lancet (1995) 1.29

Localization of the gene for X-linked recessive type of retinitis pigmentosa (XLRP) to Xp21 by linkage analysis. Am J Hum Genet (1988) 1.28

Sequence analysis and chromosomal localization of human Cap Z. Conserved residues within the actin-binding domain may link Cap Z to gelsolin/severin and profilin protein families. J Biol Chem (1995) 1.27

Replication delay along FRA7H, a common fragile site on human chromosome 7, leads to chromosomal instability. Mol Cell Biol (2000) 1.27

Immunocytology of chiasmata and chromosomal disjunction at mouse meiosis. Chromosoma (1995) 1.27

Cloning of human genes encoding novel G protein-coupled receptors. Genomics (1994) 1.26

Uncertainty in the diagnosis of cystic fibrosis: possible role of in vivo nasal potential difference measurements. J Pediatr (1998) 1.26

Cytogenetic rearrangements involving the loss of the Sonic Hedgehog gene at 7q36 cause holoprosencephaly. Hum Genet (1997) 1.25

Lens-specific promoter activity of a mouse gamma-crystallin gene. Mol Cell Biol (1985) 1.24

cAMP-inducible chloride conductance in mouse fibroblast lines stably expressing the human cystic fibrosis transmembrane conductance regulator. Proc Natl Acad Sci U S A (1991) 1.23

Signal for T-cell differentiation to a CD4 cell lineage is delivered by CD4 transmembrane region and/or cytoplasmic tail. Nature (1992) 1.23

Expression and nuclear localization of BLM, a chromosome stability protein mutated in Bloom's syndrome, suggest a role in recombination during meiotic prophase. J Cell Sci (2000) 1.23