Literature DB >> 11641464

Population-based screening for rare mutations: high-throughput DNA extraction and molecular amplification from Guthrie cards.

A Hamvas1, M Trusgnich, H Brice, J Baumgartner, Y Hong, L M Nogee, F S Cole.   

Abstract

To determine the population-based frequency of a rare mutation (the 121ins2 mutation in the surfactant protein B gene), we developed high-throughput techniques to extract reliably and rapidly amplifiable DNA from Guthrie cards. Using a 3-mm punch from each of 10,044 Guthrie cards obtained from the Missouri Department of Health, we extracted DNA with deionized water by heating in the presence of 2% Chelex in a 96-well format. Average yield of DNA from each punch was 52.6 +/- 21 microg. Using 36mer primers and a 10-microL reaction volume, we amplified a 354-bp fragment of the surfactant protein B gene that contained the mutation and identified the mutation by its susceptibility to restriction enzyme digestion with SfuI. The procedure required 5 h per 96 samples but only 2 h of technician time. The amplification rate on the first attempt was 99.2%. Based on detection of eight individuals heterozygous for the mutation (confirmed by direct sequencing), we estimate the allele frequency to be 0.8/1000 individuals, an estimate not significantly different from previous estimates based on independent methods. High-throughput DNA extraction and amplification will permit establishment of DNA banks as well as efficient estimation of population-based genotype frequency for both rare and common genetic disorders.

Entities:  

Mesh:

Substances:

Year:  2001        PMID: 11641464     DOI: 10.1203/00006450-200111000-00021

Source DB:  PubMed          Journal:  Pediatr Res        ISSN: 0031-3998            Impact factor:   3.756


  17 in total

1.  Population and disease-based prevalence of the common mutations associated with surfactant deficiency.

Authors:  Tami H Garmany; Jennifer A Wambach; Hillary B Heins; Julie M Watkins-Torry; Daniel J Wegner; Kate Bennet; Ping An; Garland Land; Ola D Saugstad; Howard Henderson; Lawrence M Nogee; F Sessions Cole; Aaron Hamvas
Journal:  Pediatr Res       Date:  2008-06       Impact factor: 3.756

2.  Recombination as a mechanism for sporadic mutation in the surfactant protein-C gene.

Authors:  Amy D McBee; Daniel J Wegner; Christopher S Carlson; Jennifer A Wambach; Ping Yang; Hillary B Heins; Ola D Saugstad; Michelle A Trusgnich; Julie Watkins-Torry; Lawrence M Nogee; Howard Henderson; F Sessions Cole; Aaron Hamvas
Journal:  Pediatr Pulmonol       Date:  2008-05

3.  Single ABCA3 mutations increase risk for neonatal respiratory distress syndrome.

Authors:  Jennifer A Wambach; Daniel J Wegner; Kelcey Depass; Hillary Heins; Todd E Druley; Robi D Mitra; Ping An; Qunyuan Zhang; Lawrence M Nogee; F Sessions Cole; Aaron Hamvas
Journal:  Pediatrics       Date:  2012-11-19       Impact factor: 7.124

4.  Diffuse lung disease in children: summary of a scientific conference.

Authors:  Aaron Hamvas; Robin Deterding; William E Balch; David A Schwartz; Kurt H Albertine; Jeffrey A Whitsett; Wellington V Cardoso; Darrell N Kotton; Stella Kourembanas; James S Hagood
Journal:  Pediatr Pulmonol       Date:  2013-06-24

Review 5.  An official American Thoracic Society clinical practice guideline: classification, evaluation, and management of childhood interstitial lung disease in infancy.

Authors:  Geoffrey Kurland; Robin R Deterding; James S Hagood; Lisa R Young; Alan S Brody; Robert G Castile; Sharon Dell; Leland L Fan; Aaron Hamvas; Bettina C Hilman; Claire Langston; Lawrence M Nogee; Gregory J Redding
Journal:  Am J Respir Crit Care Med       Date:  2013-08-01       Impact factor: 21.405

6.  ABCA3 mutations associated with pediatric interstitial lung disease.

Authors:  Janine E Bullard; Susan E Wert; Jeffrey A Whitsett; Michael Dean; Lawrence M Nogee
Journal:  Am J Respir Crit Care Med       Date:  2005-06-23       Impact factor: 21.405

7.  Comprehensive genetic variant discovery in the surfactant protein B gene.

Authors:  Aaron Hamvas; Daniel J Wegner; Christopher S Carlson; Kelly R Bergmann; Michelle A Trusgnich; Lucinda Fulton; Yumi Kasai; Ping An; Elaine R Mardis; Richard K Wilson; F Sessions Cole
Journal:  Pediatr Res       Date:  2007-08       Impact factor: 3.756

Review 8.  Genetic disorders of surfactant dysfunction.

Authors:  Susan E Wert; Jeffrey A Whitsett; Lawrence M Nogee
Journal:  Pediatr Dev Pathol       Date:  2009 Jul-Aug

9.  Population-based frequency of surfactant dysfunction mutations in a native Chinese cohort.

Authors:  Yu-Jun Chen; Jennifer Anne Wambach; Kelcey DePass; Daniel James Wegner; Shao-Ke Chen; Qun-Yuan Zhang; Hillary Heins; Francis Sessions Cole; Aaron Hamvas
Journal:  World J Pediatr       Date:  2015-11-07       Impact factor: 2.764

10.  Quantification of rare allelic variants from pooled genomic DNA.

Authors:  Todd E Druley; Francesco L M Vallania; Daniel J Wegner; Katherine E Varley; Olivia L Knowles; Jacqueline A Bonds; Sarah W Robison; Scott W Doniger; Aaron Hamvas; F Sessions Cole; Justin C Fay; Robi D Mitra
Journal:  Nat Methods       Date:  2009-03-01       Impact factor: 28.547

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.