TY - JOUR
T1 - Selfish supernumerary chromosome reveals its origin as a mosaic of host genome and organellar sequences
AU - Martis, Mihaela Maria
AU - Klemme, Sonja
AU - Banaei-Moghaddam, Ali Mohammad
AU - Blattner, Frank R.
AU - Macas, Jiř́i
AU - Schmutzer, Thomas
AU - Scholz, Uwe
AU - Gundlach, Heidrun
AU - Wicker, Thomas
AU - Sǐmková, Hana
AU - Novaḱ, Petr
AU - Neumann, Pavel
AU - Kubalaḱová, Marie
AU - Bauer, Eva
AU - Haseneyer, Grit
AU - Fuchs, Jörg
AU - Dolezěl, Jaroslav
AU - Stein, Nils
AU - Mayer, Klaus F.X.
AU - Houben, Andreas
PY - 2012/8/14
Y1 - 2012/8/14
N2 - 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.
AB - 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.
KW - Centromere
KW - Genome evolution
KW - Non-Mendelian chromosome transmission
KW - Promiscuous DNA
UR - http://www.scopus.com/inward/record.url?scp=84865161947&partnerID=8YFLogxK
U2 - 10.1073/pnas.1204237109
DO - 10.1073/pnas.1204237109
M3 - Article
C2 - 22847450
AN - SCOPUS:84865161947
VL - 109
SP - 13343
EP - 13346
JO - National Academy of Sciences, Proceedings
JF - National Academy of Sciences, Proceedings
SN - 0027-8424
IS - 33
ER -