Showing posts with label pubmed. Show all posts
Showing posts with label pubmed. Show all posts

Thursday, 2 August 2012

Selfish supernumerary chromosome reveals its origin as a mosaic of host genome and organellar sequences.


 2012 Jul 30. [Epub ahead of print]

Selfish supernumerary chromosome reveals its origin as a mosaic of host genome and organellar sequences.

Source

Institute of Bioinformatics and Systems Biology/Munich Information Center for Protein Sequences, Helmholtz Center Munich, German Research Center for Environmental Health, 85764 Neuherberg, Germany.

Abstract

Supernumerary B chromosomes are optional additions to the basic set of A chromosomes, and occur in all eukaryotic groups. They differ from the basic complement in morphology, pairing behavior, and inheritance and are not required for normal growth and development. The current view is that B chromosomes are parasitic elements comparable to selfish DNA, like transposons. In contrast to transposons, they are autonomously inherited independent of the host genome and have their own mechanisms of mitotic or meiotic drive. Although B chromosomes were first described a century ago, little is known about their origin and molecular makeup. The widely accepted view is that they are derived from fragments of A chromosomes and/or generated in response to interspecific hybridization. Through next-generation sequencing of sorted A and B chromosomes, we show that B chromosomes of rye are rich in gene-derived sequences, allowing us to trace their origin to fragments of A chromosomes, with the largest parts corresponding to rye chromosomes 3R and 7R. Compared with A chromosomes, B chromosomes were also found to accumulate large amounts of specific repeats and insertions of organellar DNA. The origin of rye B chromosomes occurred an estimated ∼1.1-1.3 Mya, overlapping in time with the onset of the genus Secale (1.7 Mya). We propose a comprehensive model of B chromosome evolution, including its origin by recombination of several A chromosomes followed by capturing of additional A-derived and organellar sequences and amplification of B-specific repeats.
PMID:
 
22847450
 
[PubMed - as supplied by publisher]


 
(¦sü·pər′nü·mə′rer·ē ′krō·mə′sōm)
(cell and molecular biology) A chromosome present in addition to the normal chromosome complement. Also known as accessory chromosome.


KevinL: have you thought about what you really were sequencing and mapping ? 
Read more: http://www.answers.com/topic/supernumerary-chromosome#ixzz22JMRmxt4

Saturday, 30 April 2011

Evaluation of next-generation sequencing software in mapping and assembly.

Evaluation of next-generation sequencing software in mapping and assembly.

J Hum Genet. 2011 Apr 28;

Authors: Bao S, Jiang R, Kwan W, Wang B, Ma X, Song YQ

Next-generation high-throughput DNA sequencing technologies have advanced progressively in sequence-based genomic research and novel biological applications with the promise of sequencing DNA at unprecedented speed. These new non-Sanger-based technologies feature several advantages when compared with traditional sequencing methods in terms of higher sequencing speed, lower per run cost and higher accuracy. However, reads from next-generation sequencing (NGS) platforms, such as 454/Roche, ABI/SOLiD and Illumina/Solexa, are usually short, thereby restricting the applications of NGS platforms in genome assembly and annotation. We presented an overview of the challenges that these novel technologies meet and particularly illustrated various bioinformatics attempts on mapping and assembly for problem solving. We then compared the performance of several programs in these two fields, and further provided advices on selecting suitable tools for specific biological applications.Journal of Human Genetics advance online publication, 28 April 2011; doi:10.1038/jhg.2011.43.

PMID: 21525877 [PubMed - as supplied by publisher]



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