Literature DB >> 1505963

NF1-related locus on chromosome 15.

E Legius1, D A Marchuk, B K Hall, L B Andersen, M R Wallace, F S Collins, T W Glover.   

Abstract

A neurofibromatosis type I (NF1)-related locus has been identified on chromosome 15. It contains a partial copy of the NF1 GAP-related domain, which is known to interact with the ras protooncogenes. However, the chromosome 15 sequence contains multiple deletions resulting in frameshift mutations and stop codons in several highly conserved sequence blocks. The locus on chromosome 15 therefore represents an NF1 pseudogene. This nonprocessed NF1 pseudogene may produce additional fragments in Southern blotting, pulsed-field gel, and PCR experiments with some NF1 cDNA probes or oligonucleotides. In addition, certain regions of the NF1 gene also cross-hybridize with a locus on chromosome 14. These loci must be considered in mutation analysis of patients with NF1 since aberrant findings may not always reflect changes in the NF1 gene.

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Year:  1992        PMID: 1505963     DOI: 10.1016/0888-7543(92)90055-w

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  8 in total

1.  The chAB4 and NF1-related long-range multisequence DNA families are contiguous in the centromeric heterochromatin of several human chromosomes.

Authors:  Imre Cserpán; Róbert Katona; Tünde Praznovszky; Edit Novák; Márta Rózsavölgyi; Erika Csonka; Mónika Mórocz; Katalin Fodor; Gyula Hadlaczky
Journal:  Nucleic Acids Res       Date:  2002-07-01       Impact factor: 16.971

2.  New nucleotide sequence data on the EMBL File Server.

Authors: 
Journal:  Nucleic Acids Res       Date:  1992-11-25       Impact factor: 16.971

3.  Organisation of the pericentromeric region of chromosome 15: at least four partial gene copies are amplified in patients with a proximal duplication of 15q.

Authors:  J A Fantes; S K Mewborn; C M Lese; J Hedrick; R L Brown; V Dyomin; R S K Chaganti; S L Christian; D H Ledbetter
Journal:  J Med Genet       Date:  2002-03       Impact factor: 6.318

Review 4.  Molecular genetics of neurofibromatosis type 1 (NF1).

Authors:  M H Shen; P S Harper; M Upadhyaya
Journal:  J Med Genet       Date:  1996-01       Impact factor: 6.318

5.  Scanning the first part of the neurofibromatosis type 1 gene by RNA-SSCP: identification of three novel mutations and of two new polymorphisms.

Authors:  P Gasparini; L D'Agruma; G Pio de Cillis; P Balestrazzi; R Mingarelli; L Zelante
Journal:  Hum Genet       Date:  1996-04       Impact factor: 4.132

6.  Minor lesion mutational spectrum of the entire NF1 gene does not explain its high mutability but points to a functional domain upstream of the GAP-related domain.

Authors:  R Fahsold; S Hoffmeyer; C Mischung; C Gille; C Ehlers; N Kücükceylan; M Abdel-Nour; A Gewies; H Peters; D Kaufmann; A Buske; S Tinschert; P Nürnberg
Journal:  Am J Hum Genet       Date:  2000-03       Impact factor: 11.025

7.  A Tsp509I variant in exon 13 of the neurofibromatosis type 1 (NF1) gene allows the identification of both alleles at the mRNA level.

Authors:  V Régnier; G Danglot; V C Nguyen; A Bernheim
Journal:  Hum Genet       Date:  1995-07       Impact factor: 4.132

8.  Deletions spanning the neurofibromatosis 1 gene: identification and phenotype of five patients.

Authors:  L M Kayes; W Burke; V M Riccardi; R Bennett; P Ehrlich; A Rubenstein; K Stephens
Journal:  Am J Hum Genet       Date:  1994-03       Impact factor: 11.025

  8 in total

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