Literature DB >> 9630578

Promoter analysis of the human mismatch repair gene hMSH2.

Y Iwahashi1, E Ito, Y Yanagisawa, Y Akiyama, Y Yuasa, T Onodera, K Maruyama.   

Abstract

The human DNA mismatch repair gene homologue hMSH2 is involved in hereditary nonpolyposis colorectal cancer. We isolated and characterized the 5' upstream region, about 4.4kbp, of the hMSH2 gene. This region contains CpG islands and a number of elements involved in constitutive expression, but there is no TATA-box nearby the transcription start points. This is the typical structure for many promoters of housekeeping genes. Alu sequences and mononucleotide repeats are clustered in this region and there are two transcription start points. Deletion analysis revealed that less than 300bp was sufficient to initiate transcription. Although no mutation that influences promoter activity of this region was found, a polymorphism was detected by PCR-RFLP analysis. Because informative cases (C/T heterozygous) were relatively high ( approximately 30%), this polymorphism is suitable for a marker to examine allelic losses. Copyright 1998 Elsevier Science B.V. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  1998        PMID: 9630578     DOI: 10.1016/s0378-1119(98)00187-5

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  10 in total

1.  Regulation of the human MSH6 gene by the Sp1 transcription factor and alteration of promoter activity and expression by polymorphisms.

Authors:  Isabella Gazzoli; Richard D Kolodner
Journal:  Mol Cell Biol       Date:  2003-11       Impact factor: 4.272

2.  Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study.

Authors:  Marlies J E Kempers; Roland P Kuiper; Charlotte W Ockeloen; Pierre O Chappuis; Pierre Hutter; Nils Rahner; Hans K Schackert; Verena Steinke; Elke Holinski-Feder; Monika Morak; Matthias Kloor; Reinhard Büttner; Eugene T P Verwiel; J Han van Krieken; Iris D Nagtegaal; Monique Goossens; Rachel S van der Post; Renée C Niessen; Rolf H Sijmons; Irma Kluijt; Frans B L Hogervorst; Edward M Leter; Johan J P Gille; Cora M Aalfs; Egbert J W Redeker; Frederik J Hes; Carli M J Tops; Bernadette P M van Nesselrooij; Marielle E van Gijn; Encarna B Gómez García; Diana M Eccles; David J Bunyan; Sapna Syngal; Elena M Stoffel; Julie O Culver; Melanie R Palomares; Tracy Graham; Lea Velsher; Janos Papp; Edith Oláh; Tsun L Chan; Suet Y Leung; Ad Geurts van Kessel; Lambertus A L M Kiemeney; Nicoline Hoogerbrugge; Marjolijn J L Ligtenberg
Journal:  Lancet Oncol       Date:  2010-12-08       Impact factor: 41.316

3.  hMSH2 expression is driven by AP1-dependent regulation through phorbol-ester exposure.

Authors:  Odile Humbert; Ikbel Achour; Dominique Lautier; Guy Laurent; Bernard Salles
Journal:  Nucleic Acids Res       Date:  2003-10-01       Impact factor: 16.971

4.  Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3' exons of TACSTD1.

Authors:  Marjolijn J L Ligtenberg; Roland P Kuiper; Tsun Leung Chan; Monique Goossens; Konnie M Hebeda; Marsha Voorendt; Tracy Y H Lee; Danielle Bodmer; Eveline Hoenselaar; Sandra J B Hendriks-Cornelissen; Wai Yin Tsui; Chi Kwan Kong; Han G Brunner; Ad Geurts van Kessel; Siu Tsan Yuen; J Han J M van Krieken; Suet Yi Leung; Nicoline Hoogerbrugge
Journal:  Nat Genet       Date:  2008-12-21       Impact factor: 38.330

5.  Differential MSH2 promoter methylation in blood cells of Neurofibromatosis type 1 (NF1) patients.

Authors:  Sabrina Titze; Hartmut Peters; Sandra Währisch; Thomas Harder; Katrin Guse; Annegret Buske; Sigrid Tinschert; Anja Harder
Journal:  Eur J Hum Genet       Date:  2010-01       Impact factor: 4.246

6.  Identification of Polycomb Group Protein EZH2-Mediated DNA Mismatch Repair Gene MSH2 in Human Uterine Fibroids.

Authors:  Qiwei Yang; Archana Laknaur; Lelyand Elam; Nahed Ismail; Larisa Gavrilova-Jordan; John Lue; Michael P Diamond; Ayman Al-Hendy
Journal:  Reprod Sci       Date:  2016-03-31       Impact factor: 3.060

Review 7.  Novel Implications in Molecular Diagnosis of Lynch Syndrome.

Authors:  Raffaella Liccardo; Marina De Rosa; Paola Izzo; Francesca Duraturo
Journal:  Gastroenterol Res Pract       Date:  2017-01-29       Impact factor: 2.260

8.  Germline MLH1, MSH2 and MSH6 variants in Brazilian patients with colorectal cancer and clinical features suggestive of Lynch Syndrome.

Authors:  Nayê Balzan Schneider; Tatiane Pastor; André Escremim de Paula; Maria Isabel Achatz; Ândrea Ribeiro Dos Santos; Fernanda Sales Luiz Vianna; Clévia Rosset; Manuela Pinheiro; Patricia Ashton-Prolla; Miguel Ângelo Martins Moreira; Edenir Inêz Palmero
Journal:  Cancer Med       Date:  2018-03-25       Impact factor: 4.452

9.  The association between genetic variants in hMLH1 and hMSH2 and the development of sporadic colorectal cancer in the Danish population.

Authors:  Lise Lotte Christensen; Bo E Madsen; Friedrik P Wikman; Carsten Wiuf; Karen Koed; Anne Tjønneland; Anja Olsen; Ann-Christine Syvänen; Claus L Andersen; Torben F Orntoft
Journal:  BMC Med Genet       Date:  2008-06-11       Impact factor: 2.103

10.  WRN Germline Mutation Is the Likely Inherited Etiology of Various Cancer Types in One Iranian Family.

Authors:  Mahnaz Norouzi; Mohammad Shafiei; Zeinab Abdollahi; Paniz Miar; Hamid Galehdari; Mohammad Hasan Emami; Mehrdad Zeinalian; Mohammad Amin Tabatabaiefar
Journal:  Front Oncol       Date:  2021-06-07       Impact factor: 6.244

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.