Literature DB >> 8178828

Tetrasomy 15q: two marker chromosomes with no detectable alpha-satellite DNA.

E Blennow1, H Telenius, D de Vos, C Larsson, P Henriksson, O Johansson, N P Carter, M Nordenskjöld.   

Abstract

Two patients with specific and similar phenotypes were both found to have an unusual marker chromosome present in 70%-80% of their lymphocytes at routine cytogenetic examination. The marker chromosomes were isolated by flow sorting and were amplified by degenerate oligonucleotide-primed PCR. These libraries and a cosmid probe located at 15q26 were used to characterize the marker chromosomes by FISH. Both marker chromosomes were found to consist of duplicated chromosome material from the distal part of chromosome 15q and were identified as inv dup(15) (qter-->q23::q23-->qter) and inv dup(15) (qter-->q24::q24-->qter), respectively. Hence, the markers did not include any known centromere region, and no alpha-satellite DNA could be detected at the site of the primary constriction. Tetrasomy 15q may be a new syndrome, associated with a specific type of marker chromosome. In addition, further analyses of this type of marker chromosome might give new insight into the structure and function of the mammalian centromere.

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Year:  1994        PMID: 8178828      PMCID: PMC1918253     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  28 in total

1.  Extra structurally abnormal chromosomes (ESAC) detected at amniocentesis: frequency in approximately 75,000 prenatal cytogenetic diagnoses and associations with maternal and paternal age.

Authors:  E B Hook; P K Cross
Journal:  Am J Hum Genet       Date:  1987-02       Impact factor: 11.025

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Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

4.  Characterization of supernumerary ring marker chromosomes by fluorescence in situ hybridization (FISH).

Authors:  E Blennow; G Annerén; T H Bui; E Berggren; E Asadi; M Nordenskjöld
Journal:  Am J Hum Genet       Date:  1993-08       Impact factor: 11.025

5.  Partial trisomy 15(q25qter) in two brothers.

Authors:  U Kristoffersson; B Bergwall
Journal:  Hereditas       Date:  1984       Impact factor: 3.271

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Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

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Journal:  J Genet Hum       Date:  1978-09

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Journal:  Clin Genet       Date:  1982-07       Impact factor: 4.438

9.  Cytogenetic and clinical studies in five cases of inv dup(15).

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Journal:  Hum Genet       Date:  1979-09       Impact factor: 4.132

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Authors:  D Pinkel; T Straume; J W Gray
Journal:  Proc Natl Acad Sci U S A       Date:  1986-05       Impact factor: 11.205

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  23 in total

Review 1.  Reverse painting highlights the origin of chromosome aberrations.

Authors:  Elisabeth Blennow
Journal:  Chromosome Res       Date:  2004       Impact factor: 5.239

2.  Distal Partial Trisomy 15q26 and Partial Monosomy 16p13.3 in a 36-Year-Old Male with Clinical Features of Both Chromosomal Abnormalities.

Authors:  Devin M Cox; Merlin G Butler
Journal:  Cytogenet Genome Res       Date:  2015-04-08       Impact factor: 1.636

Review 3.  Neocentromeres: new insights into centromere structure, disease development, and karyotype evolution.

Authors:  Owen J Marshall; Anderly C Chueh; Lee H Wong; K H Andy Choo
Journal:  Am J Hum Genet       Date:  2008-02       Impact factor: 11.025

Review 4.  Centromere DNA dynamics: latent centromeres and neocentromere formation.

Authors:  K H Choo
Journal:  Am J Hum Genet       Date:  1997-12       Impact factor: 11.025

5.  Additional complexity on human chromosome 15q: identification of a set of newly recognized duplicons (LCR15) on 15q11-q13, 15q24, and 15q26.

Authors:  M A Pujana; M Nadal; M Gratacòs; B Peral; K Csiszar; R González-Sarmiento; L Sumoy; X Estivill
Journal:  Genome Res       Date:  2001-01       Impact factor: 9.043

Review 6.  Molecular cytogenetic analysis of eight inversion duplications of human chromosome 13q that each contain a neocentromere.

Authors:  P E Warburton; M Dolled; R Mahmood; A Alonso; S Li; K Naritomi; T Tohma; T Nagai; T Hasegawa; H Ohashi; L C Govaerts; B H Eussen; J O Van Hemel ; C Lozzio; S Schwartz; J J Dowhanick-Morrissette; N B Spinner; H Rivera; J A Crolla; C Yu; D Warburton
Journal:  Am J Hum Genet       Date:  2000-04-24       Impact factor: 11.025

7.  Multiplex ligation dependent probe amplification (MLPA) for rapid distinction between unique sequence positive and negative marker chromosomes in prenatal diagnosis.

Authors:  Diane Van Opstal; Marjan Boter; Petra Noomen; Malgorzata Srebniak; Guus Hamers; Robert-Jan H Galjaard
Journal:  Mol Cytogenet       Date:  2011-01-14       Impact factor: 2.009

8.  An unusual dicentric Y chromosome with a functional centromere with no detectable alpha-satellite.

Authors:  N Bukvic; F Susca; M Gentile; E Tangari; A Ianniruberto; G Guanti
Journal:  Hum Genet       Date:  1996-04       Impact factor: 4.132

9.  A stable acentric marker chromosome: possible existence of an intercalary ancient centromere at distal 8p.

Authors:  H Ohashi; K Wakui; K Ogawa; T Okano; N Niikawa; Y Fukushima
Journal:  Am J Hum Genet       Date:  1994-12       Impact factor: 11.025

10.  Identification of the origin of double minutes in normal human cells by laser-based chromosome microdissection approach.

Authors:  E Rajcan-Separovic; H S Wang; M D Speevak; L Janes; R G Korneluk; K Wakasa; J E Ikeda
Journal:  Hum Genet       Date:  1995-07       Impact factor: 4.132

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