In silico cloning of mouse Muc5b gene and upregulation of its expression in mouse asthma model

Citation
Y. Chen et al., In silico cloning of mouse Muc5b gene and upregulation of its expression in mouse asthma model, AM J R CRIT, 164(6), 2001, pp. 1059-1066
Citations number
27
Categorie Soggetti
Cardiovascular & Respiratory Systems","da verificare
Journal title
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE
ISSN journal
1073449X → ACNP
Volume
164
Issue
6
Year of publication
2001
Pages
1059 - 1066
Database
ISI
SICI code
1073-449X(20010915)164:6<1059:ISCOMM>2.0.ZU;2-O
Abstract
Using a BLAST-searching approach, we identified a mouse expressed sequence tag (EST) clone (AA038672) showing great similarity to the 3' end of the hu man MUC5B gene. The clone was named "3pmmuc5b-1" after complete nucleotide sequencing (Genbank Accession, AF369933). A subsequent search of the mouse genome database with the 3pmmuc5b-1 sequence identified two overlapping gen omic clones (AC020817 and AC020794) that contained the sequence of both 3pm muc5b-1 and the mouse Muc5ac gene. Like their human homologs, the genomic o rder of the mouse Muc genes is 5'-Muc5ac-Muc5b-3'. These results suggest th at the newly identified EST clone, 3pmmuc5b-1, is part of the 3' portion of the mouse Muc5b gene. In situ hybridization demonstrated that this putativ e mouse Muc5b message was expressed in a restricted manner in the sublingua l gland region of the tongue and the submucosal gland region of the mouse t rachea in a normal animal. However, the gene expression was greatly enhance d in airway surface epithelium and the submucosal gland region in ovalbumin -induced asthmatic mice. These results were consistent with previous studie s of human airway tissues. We therefore conclude that this newly cloned mou se Muc5b gene could be used as a marker for studying aberrant mucin gene ex pression in mouse models of various airway diseases.