Mechanisms and consequences of small supernumerary marker chromosomes: from Barbara McClintock to modern genetic-counseling issues.

Abstract:

:Supernumerary marker chromosomes (SMCs) are common, but their molecular content and mechanism of origin are often not precisely characterized. We analyzed all centromere regions to identify the junction between the unique chromosome arm and the pericentromeric repeats. A molecular-ruler clone panel for each chromosome arm was developed and used for the design of a custom oligonucleotide array. Of 27 nonsatellited SMCs analyzed by array comparative genomic hybridization (aCGH) and/or fluorescence in situ hybridization (FISH), seven (approximately 26%) were shown to be unique sequence negative. Of the 20 unique-sequence-positive SMCs, the average unique DNA content was approximately 6.5 Mb (range 0.3-22.2 Mb) and 33 known genes (range 0-149). Of the 14 informative nonacrocentric SMCs, five (approximately 36%) contained unique DNA from both the p and q arms, whereas nine (approximately 64%) contained unique DNA from only one arm. The latter cases are consistent with ring-chromosome formation by centromere misdivision, as first described by McClintock in maize. In one case, a r(4) containing approximately 4.4 Mb of unique DNA from 4p was also present in the proband's mother. However, FISH revealed a cryptic deletion in one chromosome 4 and reduced alpha satellite in the del(4) and r(4), indicating that the mother was a balanced ring and deletion carrier. Our data, and recent reports in the literature, suggest that this "McClintock mechanism" of small-ring formation might be the predominant mechanism of origin. Comprehensive analysis of SMCs by aCGH and FISH can distinguish unique-negative from unique-positive cases, determine the precise gene content, and provide information on mechanism of origin, inheritance, and recurrence risk.

journal_name

Am J Hum Genet

authors

Baldwin EL,May LF,Justice AN,Martin CL,Ledbetter DH

doi

10.1016/j.ajhg.2007.10.013

subject

Has Abstract

pub_date

2008-02-01 00:00:00

pages

398-410

issue

2

eissn

0002-9297

issn

1537-6605

pii

S0002-9297(08)00092-X

journal_volume

82

pub_type

杂志文章
  • The interleukin 1 gene cluster contains a major susceptibility locus for ankylosing spondylitis.

    abstract::Ankylosing spondylitis (AS) is a common and highly heritable inflammatory arthropathy. Although the gene HLA-B27 is almost essential for the inheritance of the condition, it alone is not sufficient to explain the pattern of familial recurrence of the disease. We have previously demonstrated suggestive linkage of AS to...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:10.1086/424695

    authors: Timms AE,Crane AM,Sims AM,Cordell HJ,Bradbury LA,Abbott A,Coyne MR,Beynon O,Herzberg I,Duff GW,Calin A,Cardon LR,Wordsworth BP,Brown MA

    更新日期:2004-10-01 00:00:00

  • BMP9 mutations cause a vascular-anomaly syndrome with phenotypic overlap with hereditary hemorrhagic telangiectasia.

    abstract::Hereditary hemorrhagic telangiectasia (HHT), the most common inherited vascular disorder, is caused by mutations in genes involved in the transforming growth factor beta (TGF-β) signaling pathway (ENG, ACVRL1, and SMAD4). Yet, approximately 15% of individuals with clinical features of HHT do not have mutations in thes...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:10.1016/j.ajhg.2013.07.004

    authors: Wooderchak-Donahue WL,McDonald J,O'Fallon B,Upton PD,Li W,Roman BL,Young S,Plant P,Fülöp GT,Langa C,Morrell NW,Botella LM,Bernabeu C,Stevenson DA,Runo JR,Bayrak-Toydemir P

    更新日期:2013-09-05 00:00:00

  • Spinal muscular atrophy associated with progressive myoclonic epilepsy is caused by mutations in ASAH1.

    abstract::Spinal muscular atrophy (SMA) is a clinically and genetically heterogeneous disease characterized by the degeneration of lower motor neurons. The most frequent form is linked to mutations in SMN1. Childhood SMA associated with progressive myoclonic epilepsy (SMA-PME) has been reported as a rare autosomal-recessive con...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:10.1016/j.ajhg.2012.05.001

    authors: Zhou J,Tawk M,Tiziano FD,Veillet J,Bayes M,Nolent F,Garcia V,Servidei S,Bertini E,Castro-Giner F,Renda Y,Carpentier S,Andrieu-Abadie N,Gut I,Levade T,Topaloglu H,Melki J

    更新日期:2012-07-13 00:00:00

  • Population heterogeneity of the Hpa I restriction site associated with the beta globin gene: implications for prenatal diagnosis.

    abstract::The Hpa I restriction endonuclease site polymorphism that results in some human beta globin genes being contained in a 13-kilobase (kb) DNA restriction fragment rather than in the usual 7.6-kb fragment has been reported to be in linkage disequilibrium with the beta S mutation. The frequency of the 13-kb fragment among...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:

    authors: Panny SR,Scott AF,Smith KD,Phillips JA 3rd,Kazazian HH Jr,Talbot CC Jr,Boehm CD

    更新日期:1981-01-01 00:00:00

  • Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35.

    abstract::Isolated or nonsyndromic cleft lip with or without cleft palate (CL/P) is a common birth defect with a complex etiology. A 10-cM genome scan of 388 extended multiplex families with CL/P from seven diverse populations (2,551 genotyped individuals) revealed CL/P genes in six chromosomal regions, including a novel region...

    journal_title:American journal of human genetics

    pub_type: 杂志文章,meta分析

    doi:10.1086/422475

    authors: Marazita ML,Murray JC,Lidral AC,Arcos-Burgos M,Cooper ME,Goldstein T,Maher BS,Daack-Hirsch S,Schultz R,Mansilla MA,Field LL,Liu YE,Prescott N,Malcolm S,Winter R,Ray A,Moreno L,Valencia C,Neiswanger K,Wyszynski DF,

    更新日期:2004-08-01 00:00:00

  • Proportion of genome shared identical by descent by relatives: concept, computation, and applications.

    abstract::One widely used measure of genetic similarity for pairs of relatives is gene identity-by-descent (IBD) sharing. Genes that are copies of a single gene in a common ancestor of the individuals who now carry them are said to be IBD. One obvious extension of the IBD concept is IBD gene(s) shared by more than two individua...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:

    authors: Guo SW

    更新日期:1995-06-01 00:00:00

  • Studies on phenotypic complementation of ataxia-telangiectasia cells by chromosome transfer.

    abstract::Cells derived from patients with the cancer-prone inherited disorder ataxia-telangiectasia (A-T) show an abnormal response to ionizing radiation-induced DNA damage, such as an increased cell killing and a diminished inhibition of DNA synthesis. The enhanced killing of A-T (group D) cells by X-rays can be corrected by ...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:

    authors: Jongmans W,Verhaegh GW,Jaspers NG,Oshimura M,Stanbridge EJ,Lohman PH,Zdzienicka MZ

    更新日期:1995-02-01 00:00:00

  • Genetic variation in radiation-induced expression phenotypes.

    abstract::Studies have demonstrated that natural variation in the expression level of genes at baseline is extensive, and the determinants of this variation can be mapped by a genetic-linkage approach. In this study, we used lymphoblastoid cells to explore the variation in radiation-induced transcriptional changes. We found tha...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:10.1086/425221

    authors: Correa CR,Cheung VG

    更新日期:2004-11-01 00:00:00

  • Leaky splicing mutation in the acid maltase gene is associated with delayed onset of glycogenosis type II.

    abstract::An autosomal recessive deficiency of acid alpha-glucosidase (GAA), type II glycogenosis, is genetically and clinically heterogeneous. The discovery of an enzyme-inactivating genomic deletion of exon 18 in three unrelated genetic compound patients--two infants and an adult--provided a rare opportunity to analyze the ef...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:

    authors: Boerkoel CF,Exelbert R,Nicastri C,Nichols RC,Miller FW,Plotz PH,Raben N

    更新日期:1995-04-01 00:00:00

  • Truncating Mutations of MAGEL2, a Gene within the Prader-Willi Locus, Are Responsible for Severe Arthrogryposis.

    abstract::Arthrogryposis multiplex congenita (AMC) is characterized by the presence of multiple joint contractures resulting from reduced or absent fetal movement. Here, we report two unrelated families affected by lethal AMC. By genetic mapping and whole-exome sequencing in a multiplex family, a heterozygous truncating MAGEL2 ...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:10.1016/j.ajhg.2015.08.010

    authors: Mejlachowicz D,Nolent F,Maluenda J,Ranjatoelina-Randrianaivo H,Giuliano F,Gut I,Sternberg D,Laquerrière A,Melki J

    更新日期:2015-10-01 00:00:00

  • How rapidly does the human mitochondrial genome evolve?

    abstract::The results of an empirical nucleotide-sequencing approach indicate that the evolution of the human mitochondrial noncoding D-loop is both more rapid and more complex than is revealed by standard phylogenetic approaches. The nucleotide sequence of the D-loop region of the mitochondrial genome was determined for 45 mem...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:

    authors: Howell N,Kubacka I,Mackey DA

    更新日期:1996-09-01 00:00:00

  • Walking the interactome for prioritization of candidate disease genes.

    abstract::The identification of genes associated with hereditary disorders has contributed to improving medical care and to a better understanding of gene functions, interactions, and pathways. However, there are well over 1500 Mendelian disorders whose molecular basis remains unknown. At present, methods such as linkage analys...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:10.1016/j.ajhg.2008.02.013

    authors: Köhler S,Bauer S,Horn D,Robinson PN

    更新日期:2008-04-01 00:00:00

  • Comparative genomics and the evolution of human mitochondrial DNA: assessing the effects of selection.

    abstract::This article provides evidence that selection has been a significant force during the evolution of the human mitochondrial genome. Both gene-by-gene and whole-genome approaches were used here to assess selection in the 560 mitochondrial DNA (mtDNA) coding-region sequences that were used previously for reduced-median-n...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:10.1086/381505

    authors: Elson JL,Turnbull DM,Howell N

    更新日期:2004-02-01 00:00:00

  • A note on Cannings and Thompson's sequential sampling scheme for pedigrees.

    abstract::We consider sequential sampling of pedigrees for genetic analysis. Cannings and Thompson (1977) gave simple, general guidelines for valid sequential sampling schemes. We show that their formulation of the likelihood contains an error, which is, however, easily corrected so as to maintain the validity of the sequential...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:

    authors: Hodge SE,Boehnke M

    更新日期:1986-08-01 00:00:00

  • Unusual splice-site mutations in the RSK2 gene and suggestion of genetic heterogeneity in Coffin-Lowry syndrome.

    abstract::Coffin-Lowry syndrome (CLS) is a syndromic form of X-linked mental retardation that is characterized, in male patients, by psychomotor and growth retardation and various skeletal anomalies. Typical facial changes and specific clinical and radiological hand aspects exhibited by patients are essential clues for the diag...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:10.1086/340607

    authors: Zeniou M,Pannetier S,Fryns JP,Hanauer A

    更新日期:2002-06-01 00:00:00

  • Trans-ethnic Fine Mapping Highlights Kidney-Function Genes Linked to Salt Sensitivity.

    abstract::We analyzed genome-wide association studies (GWASs), including data from 71,638 individuals from four ancestries, for estimated glomerular filtration rate (eGFR), a measure of kidney function used to define chronic kidney disease (CKD). We identified 20 loci attaining genome-wide-significant evidence of association (p...

    journal_title:American journal of human genetics

    pub_type: 杂志文章,meta分析

    doi:10.1016/j.ajhg.2016.07.012

    authors: Mahajan A,Rodan AR,Le TH,Gaulton KJ,Haessler J,Stilp AM,Kamatani Y,Zhu G,Sofer T,Puri S,Schellinger JN,Chu PL,Cechova S,van Zuydam N,SUMMIT Consortium.,BioBank Japan Project.,Arnlov J,Flessner MF,Giedraitis V,Heath

    更新日期:2016-09-01 00:00:00

  • Functional variants in the promoter region of Chitinase 3-like 1 (CHI3L1) and susceptibility to schizophrenia.

    abstract::The chitinase 3-like 1 gene (CHI3L1) is abnormally expressed in the hippocampus of subjects with schizophrenia and may be involved in the cellular response to various environmental events that are reported to increase the risk of schizophrenia. Here, we provide evidence that the functional variants at the CHI3L1 locus...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:10.1086/510438

    authors: Zhao X,Tang R,Gao B,Shi Y,Zhou J,Guo S,Zhang J,Wang Y,Tang W,Meng J,Li S,Wang H,Ma G,Lin C,Xiao Y,Feng G,Lin Z,Zhu S,Xing Y,Sang H,St Clair D,He L

    更新日期:2007-01-01 00:00:00

  • A yeast artificial chromosome telomere clone spanning a possible location of the Huntington disease gene.

    abstract::The Huntington disease (HD) gene has been mapped to the most distal subband of chromosome 4p. Analysis of recombination events has not provided an unequivocal location of the HD gene, but it indicates a position very close to the telomere as one possibility. We have constructed a yeast artificial chromosome (YAC) vect...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:

    authors: Bates GP,MacDonald ME,Baxendale S,Sedlacek Z,Youngman S,Romano D,Whaley WL,Allitto BA,Poustka A,Gusella JF

    更新日期:1990-04-01 00:00:00

  • Evidence that methylation of the FMR-I locus is responsible for variable phenotypic expression of the fragile X syndrome.

    abstract::DNA at the FMR-1 locus was analyzed by Southern blot using probe StB12.3 in an unusual fragile X family with six brothers, three of whom are affected with fragile X to varying degrees, two of whom are nonpenetrant carriers, and one of whom is unaffected. Fragile X chromosome studies, detailed physical examinations, an...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:

    authors: McConkie-Rosell A,Lachiewicz AM,Spiridigliozzi GA,Tarleton J,Schoenwald S,Phelan MC,Goonewardena P,Ding X,Brown WT

    更新日期:1993-10-01 00:00:00

  • Contrasting linkage-disequilibrium patterns between cases and controls as a novel association-mapping method.

    abstract::Identification and description of genetic variation underlying disease susceptibility, efficacy, and adverse reactions to drugs remains a difficult problem. One of the important steps in the analysis of variation in a candidate region is the characterization of linkage disequilibrium (LD). In a region of genetic assoc...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:10.1086/503710

    authors: Zaykin DV,Meng Z,Ehm MG

    更新日期:2006-05-01 00:00:00

  • A DNA polymorphism in close physical linkage with the proopiomelanocortin gene.

    abstract::Cellular DNAs from a panel of 20 unrelated individuals were screened for restriction fragment length polymorphisms (RFLP) with a DNA probe containing the first exon of the proopiomelanocortin gene (POMC), which has been assigned to chromosome 2p23-25. Digestion with the restriction endonuclease Sst 1 revealed a high f...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:

    authors: Feder J,Migone N,Chang AC,Cochet M,Cohen SN,Cann H,Cavalli-Sforza LL

    更新日期:1983-11-01 00:00:00

  • HLA antigens in cardiomyopathic Chilean chagasics.

    abstract::The distribution of HLA antigens in a sample of 124 Chagas serologically positive Chilean individuals was studied. The sample was subdivided according to the presence or absence of chagasic cardiomyopathy, in order to search for genetic differences associated with this pathological condition. The frequency of antigen ...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:

    authors: Llop E,Rothhammer F,Acuña M,Apt W

    更新日期:1988-11-01 00:00:00

  • Linkage disequilibrium mapping of the gene for Margarita Island ectodermal dysplasia (ED4) to 11q23.

    abstract::Margarita Island ectodermal dysplasia (ED4) is an autosomal recessive disorder characterized by unusual facies, dental anomalies, hypotrichosis, palmoplantar hyperkeratosis and onychodysplasia, syndactyly, and cleft lip/cleft palate. We have used an affected-only DNA-pooling strategy to carry out linkage disequilibriu...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:10.1086/302072

    authors: Suzuki K,Bustos T,Spritz RA

    更新日期:1998-10-01 00:00:00

  • Improved power by use of a weighted score test for linkage disequilibrium mapping.

    abstract::Association studies offer an exciting approach to finding underlying genetic variants of complex human diseases. However, identification of genetic variants still includes difficult challenges, and it is important to develop powerful new statistical methods. Currently, association methods may depend on single-locus an...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:10.1086/511312

    authors: Wang T,Elston RC

    更新日期:2007-02-01 00:00:00

  • A high-density screen for linkage in multiple sclerosis.

    abstract::To provide a definitive linkage map for multiple sclerosis, we have genotyped the Illumina BeadArray linkage mapping panel (version 4) in a data set of 730 multiplex families of Northern European descent. After the application of stringent quality thresholds, data from 4,506 markers in 2,692 individuals were included ...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:10.1086/444547

    authors: Sawcer S,Ban M,Maranian M,Yeo TW,Compston A,Kirby A,Daly MJ,De Jager PL,Walsh E,Lander ES,Rioux JD,Hafler DA,Ivinson A,Rimmler J,Gregory SG,Schmidt S,Pericak-Vance MA,Akesson E,Hillert J,Datta P,Oturai A,Ryder L

    更新日期:2005-09-01 00:00:00

  • Testing for association between disease and linked marker loci: a log-linear-model analysis.

    abstract::One approach frequently used for identifying genetic factors involved in the process of a complex disease is the comparison of patients and controls for a number of genetic markers near a candidate gene. The analysis of such association studies raises some specific problems because of the fact that genotypic and not g...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:

    authors: Tiret L,Amouyel P,Rakotovao R,Cambien F,Ducimetière P

    更新日期:1991-05-01 00:00:00

  • Testing association between candidate-gene markers and phenotype in related individuals, by use of estimating equations.

    abstract::Association studies are one of the major strategies for identifying genetic factors underlying complex traits. In samples of related individuals, conventional statistical procedures are not valid for testing association, and maximum likelihood (ML) methods have to be used, but they are computationally demanding and ar...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:10.1086/513895

    authors: Trégouët DA,Ducimetière P,Tiret L

    更新日期:1997-07-01 00:00:00

  • Mutant GlialCAM causes megalencephalic leukoencephalopathy with subcortical cysts, benign familial macrocephaly, and macrocephaly with retardation and autism.

    abstract::Megalencephalic leukoencephalopathy with subcortical cysts (MLC) is a leukodystrophy characterized by early-onset macrocephaly and delayed-onset neurological deterioration. Recessive MLC1 mutations are observed in 75% of patients with MLC. Genetic-linkage studies failed to identify another gene. We recently showed tha...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:10.1016/j.ajhg.2011.02.009

    authors: López-Hernández T,Ridder MC,Montolio M,Capdevila-Nortes X,Polder E,Sirisi S,Duarri A,Schulte U,Fakler B,Nunes V,Scheper GC,Martínez A,Estévez R,van der Knaap MS

    更新日期:2011-04-08 00:00:00

  • Biases and reconciliation in estimates of linkage disequilibrium in the human genome.

    abstract::Genetic association studies of common disease often rely on linkage disequilibrium (LD) along the human genome and in the population under study. Although understanding the characteristics of this correlation has been the focus of many large-scale surveys (culminating in genomewide haplotype maps), the results of diff...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:10.1086/502803

    authors: Pe'er I,Chretien YR,de Bakker PI,Barrett JC,Daly MJ,Altshuler DM

    更新日期:2006-04-01 00:00:00

  • Privacy Risks from Genomic Data-Sharing Beacons.

    abstract::The human genetics community needs robust protocols that enable secure sharing of genomic data from participants in genetic research. Beacons are web servers that answer allele-presence queries--such as "Do you have a genome that has a specific nucleotide (e.g., A) at a specific genomic position (e.g., position 11,272...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:10.1016/j.ajhg.2015.09.010

    authors: Shringarpure SS,Bustamante CD

    更新日期:2015-11-05 00:00:00