Literature DB >> 2831714

Localization of gelsolin proximal to ABL on chromosome 9.

D J Kwiatkowski1, C A Westbrook, G A Bruns, C C Morton.   

Abstract

Gelsolin is a plasma and cytoskeletal protein that severs actin filaments and is regulated by both Ca+2 and polyphosphoinositides. The two forms of gelsolin are encoded by a single gene and derived through alternative message splicing. By Southern blot analysis of somatic cell hybrids and in situ chromosomal localization, we demonstrate that the gelsolin gene is present on human chromosome 9 in bands q32-q34. In situ hybridization of gelsolin to cells containing a Philadelphia chromosome [(9;22)(q34;q11)], as well as Southern blot analysis of K562 cell DNA, indicates that gelsolin is centromeric to the ABL locus in 9q34. Southern blot analysis of NotI-digested, pulsed-field gel electrophoresis-separated DNA indicates the gelsolin gene is greater than or equal to 40 kb centromeric to ABL. These studies and standard Southern blot analysis of digested DNA also indicate that the NotI restriction site contained in the gelsolin gene is uncleavable in DNA from white blood cells and hematopoietic cell lines.

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Year:  1988        PMID: 2831714      PMCID: PMC1715225     

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


  33 in total

1.  Segregation of ABO, AK1 and ACONs in families with abnormalities of chromosome 9.

Authors:  P J Cook; E B Robson; K E Buckton; C A Slaughter; J E Gray; C E Blank; F E James; M A Ridler; J Insley; M Hultén
Journal:  Ann Hum Genet       Date:  1978-01       Impact factor: 1.670

2.  BrdU-33258 Hoechst analysis of DNA replication in human lymphocytes with supernumerary or structurally abnormal X chromosomes.

Authors:  S A Latt; H F Willard; P S Gerald
Journal:  Chromosoma       Date:  1976-08-17       Impact factor: 4.316

3.  F-Actin-depolymerizing activity of human serum.

Authors:  R Norberg; R Thorstensson; G Utter; A Fagraeus
Journal:  Eur J Biochem       Date:  1979-10-15

4.  Letter: A new consistent chromosomal abnormality in chronic myelogenous leukaemia identified by quinacrine fluorescence and Giemsa staining.

Authors:  J D Rowley
Journal:  Nature       Date:  1973-06-01       Impact factor: 49.962

5.  Control of cytoplasmic actin gel-sol transformation by gelsolin, a calcium-dependent regulatory protein.

Authors:  H L Yin; T P Stossel
Journal:  Nature       Date:  1979-10-18       Impact factor: 49.962

6.  Establishment and characterization of a human histiocytic lymphoma cell line (U-937).

Authors:  C Sundström; K Nilsson
Journal:  Int J Cancer       Date:  1976-05-15       Impact factor: 7.396

7.  The first intron in the human c-abl gene is at least 200 kilobases long and is a target for translocations in chronic myelogenous leukemia.

Authors:  A Bernards; C M Rubin; C A Westbrook; M Paskind; D Baltimore
Journal:  Mol Cell Biol       Date:  1987-09       Impact factor: 4.272

8.  Human lysosomal genes: arylsulfatase A and beta-galactosidase.

Authors:  G A Bruns; B J Mintz; A C Leary; V M Regina; P S Gerald
Journal:  Biochem Genet       Date:  1979-12       Impact factor: 1.890

9.  An actin-destabilizing factor is present in human plasma.

Authors:  C Chaponnier; R Borgia; E Rungger-Brändle; R Weil; G Gabbiani
Journal:  Experientia       Date:  1979-08-15

10.  Identification of gelsolin, a Ca2+-dependent regulatory protein of actin gel-sol transformation, and its intracellular distribution in a variety of cells and tissues.

Authors:  H L Yin; J H Albrecht; A Fattoum
Journal:  J Cell Biol       Date:  1981-12       Impact factor: 10.539

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  17 in total

Review 1.  The Finnish Disease Heritage III: the individual diseases.

Authors:  Reijo Norio
Journal:  Hum Genet       Date:  2003-03-08       Impact factor: 4.132

2.  Dinucleotide repeat polymorphism at the GSN locus (9q32-34).

Authors:  D J Kwiatkowski; S Perman
Journal:  Nucleic Acids Res       Date:  1991-02-25       Impact factor: 16.971

Review 3.  Mouse chromosome 2.

Authors:  L D Siracusa; C M Abbott
Journal:  Mamm Genome       Date:  1991       Impact factor: 2.957

4.  Amyloid in familial amyloidosis, Finnish type, is antigenically and structurally related to gelsolin.

Authors:  M Haltia; J Ghiso; F Prelli; G Gallo; S Kiuru; H Somer; J Palo; B Frangione
Journal:  Am J Pathol       Date:  1990-06       Impact factor: 4.307

5.  Plasma gelsolin protects HIV-1 gp120-induced neuronal injury via voltage-gated K+ channel Kv2.1.

Authors:  Han Liu; Jianuo Liu; Shangdong Liang; Huangui Xiong
Journal:  Mol Cell Neurosci       Date:  2013-11       Impact factor: 4.314

Review 6.  The genetics of primary torsion dystonia.

Authors:  U Müller; K G Kupke
Journal:  Hum Genet       Date:  1990-01       Impact factor: 4.132

7.  Gelsolin-related amyloidosis. Identification of the amyloid protein in Finnish hereditary amyloidosis as a fragment of variant gelsolin.

Authors:  C P Maury
Journal:  J Clin Invest       Date:  1991-04       Impact factor: 14.808

8.  Finnish type of familial amyloidosis: cosegregation of Asp187----Asn mutation of gelsolin with the disease in three large families.

Authors:  T Hiltunen; S Kiuru; V Hongell; T Heliö; J Palo; L Peltonen
Journal:  Am J Hum Genet       Date:  1991-09       Impact factor: 11.025

9.  Gelsolin gene expression is upregulated in damaged rat and human livers within non-parenchymal cells and not in hepatocytes.

Authors:  Katrin Neubauer; Yacoov Baruch; Alexander Lindhorst; Bernhard Saile; Giuliano Ramadori
Journal:  Histochem Cell Biol       Date:  2003-08-28       Impact factor: 4.304

10.  Lewy bodies are immunoreactive with antibodies raised to gelsolin related amyloid-Finnish type.

Authors:  T Wisniewski; M Haltia; J Ghiso; B Frangione
Journal:  Am J Pathol       Date:  1991-05       Impact factor: 4.307

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