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1.
Neurogenetics ; 18(3): 169-174, 2017 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-28285357

RESUMO

Multiplex ligation-dependent probe amplification (MLPA) has been widely used to identify copy-number variations (CNVs), but MLPA's sensitivity and specificity in mosaic CNV detection are largely unknown. Here, we present two mosaic deletions identified by MLPA as NF1 deletion of exons 17-21 and NF2 deletion of exons 9-10. Through cDNA analysis, genomic breakpoint-spanning PCR and Sanger sequencing, we found however both NF1 and NF2 deletions are each composed of two consecutive deletions, which cannot be differentiated by MLPA. Importantly, these consecutive deletions are most likely originating from a single genomic rearrangement and have been preserved independently in different populations of cells.


Assuntos
Variações do Número de Cópias de DNA/genética , Éxons/genética , Neurofibromatose 1/genética , Neurofibromatose 2/genética , Deleção de Genes , Genoma Humano , Genômica , Humanos , Mutação/genética , Reação em Cadeia da Polimerase/métodos
2.
J Microbiol Methods ; 69(1): 161-73, 2007 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-17289189

RESUMO

The aim of this study was to analyze a total euryarchaeal community at DNA and RNA levels in a Swedish barley field with relation to soil depth (0-10 and 20-30 cm layers), soil fraction (bulk soil and rhizosphere) and time (August and November sample collection). Amplification of 16S rRNA gene using the archaeal universal A2F and Euryarchaea specific EK510R/(EURY498) primer pair, combined with denaturing gradient gel electrophoresis (DGGE), revealed distinct differences between rDNA and rRNA DGGE profiles. The soil depth, time, or rhizosphere effects did not significantly influence Archaeal community structure. Surprisingly, sequence analysis of DGGE-derived amplicons revealed the presence of Euryarchaea as well as uncultured soil Crenarchaea affiliated with group 1. In agreement, sequence comparison analyses showed that the majority of uncultured Crenarchaea group 1 had almost 100% sequence complementarity to the 3' end of the EK510R/(EURY498) primer. Therefore, we propose that EK510R/(EURY498R) is a universal archaeal primer rather than a Euryarchaea specific SSUrRNA primer. Hence, considerable care should be taken during application of this primer in studies of euryarchaeal biodiversity in soil environments.


Assuntos
Archaea/isolamento & purificação , Primers do DNA/química , DNA Arqueal/química , Hordeum , RNA Arqueal/genética , RNA Ribossômico 16S/genética , Solo , Archaea/classificação , Archaea/genética , Biodiversidade , DNA Ribossômico/química , Ecossistema , Eletroforese em Gel de Poliacrilamida , Filogenia
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