Literature DB >> 8661053

Assembly of a 1-Mb restriction-mapped cosmid contig spanning the candidate region for Finnish congenital nephrosis (NPHS1) in 19q13.1.

A S Olsen1, A Georgescu, S Johnson, A V Carrano.   

Abstract

We describe the assembly of a 1-Mb cosmid contig and restriction map spanning the candidate region for Finnish congenital nephrosis (NPHS1) in 19q13.1. The map was constructed from 16 smaller contigs assembled by fingerprinting, a BAC and a PAC clone, and 42 previously unmapped cosmids. In most cases, single-step cosmid walks were sufficient to join two previously assembled contigs, and all but one gap was filled from this cosmid contig library. The remaining gap of about 19 kb was spanned with a single BAC and a single PAC clone. EcoRI mapping of a dense set of overlapping clones validated the assembly of the map and indicated a length of 1040 kb for the contig. This high-resolution clone map provides an ideal resource for gene identification through cDNA selection, exon trapping, and DNA sequencing.

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Year:  1996        PMID: 8661053     DOI: 10.1006/geno.1996.0270

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


  6 in total

1.  Comparative maps of human 19p13.3 and mouse chromosome 10 allow identification of sequences at evolutionary breakpoints.

Authors:  R Puttagunta; L A Gordon; G E Meyer; D Kapfhamer; J E Lamerdin; P Kantheti; K M Portman; W K Chung; D E Jenne; A S Olsen; M Burmeister
Journal:  Genome Res       Date:  2000-09       Impact factor: 9.043

2.  Non-methylated Genomic Sites Coincidence Cloning (NGSCC): an approach to large scale analysis of hypomethylated CpG patterns at predetermined genomic loci.

Authors:  T Azhikina; I Gainetdinov; Yu Skvortsova; A Batrak; N Dmitrieva; E Sverdlov
Journal:  Mol Genet Genomics       Date:  2003-12-10       Impact factor: 3.291

Review 3.  Glomerular diseases: genetic causes and future therapeutics.

Authors:  Chih-Kang Chiang; Reiko Inagi
Journal:  Nat Rev Nephrol       Date:  2010-07-20       Impact factor: 28.314

4.  Methylation-free site patterns along a 1-Mb locus on Chr19 in cancerous and normal cells are similar. A new fast approach for analyzing unmethylated CCGG sites distribution.

Authors:  Tatyana Azhikina; Ildar Gainetdinov; Yulia Skvortsova; Eugene Sverdlov
Journal:  Mol Genet Genomics       Date:  2006-02-25       Impact factor: 3.291

5.  Identification and characterization of the human homologue of the short PDE4A cAMP-specific phosphodiesterase RD1 (PDE4A1) by analysis of the human HSPDE4A gene locus located at chromosome 19p13.2.

Authors:  M Sullivan; G Rena; F Begg; L Gordon; A S Olsen; M D Houslay
Journal:  Biochem J       Date:  1998-08-01       Impact factor: 3.857

6.  Induction of transcription within chromosomal DNA loops flanked by MAR elements causes an association of loop DNA with the nuclear matrix.

Authors:  Olga V Iarovaia; Sergey B Akopov; Lev G Nikolaev; Eugene D Sverdlov; Sergey V Razin
Journal:  Nucleic Acids Res       Date:  2005-07-26       Impact factor: 16.971

  6 in total

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