First published online July 7, 2006; 10.1105/tpc.106.041905
The Plant Cell 18:1791-1802 (2006)
© 2006 American Society of Plant Biologists
High Rate of Chimeric Gene Origination by Retroposition in Plant Genomes[W]
Wen Wanga,b,1,
Hongkun Zhengb,c,1,
Chuanzhu Fand,1,
Jun Lib,
Junjie Shib,e,
Zhengqiu Caib,
Guojie Zhanga,b,f,
Dongyuan Liub,
Jianguo Zhangb,
Søren Vangg,
Zhike Lub,
Gane Ka-Shu Wongb,
Manyuan Longd,2 and
Jun Wangb,c,g,2
a CAS-Max-Plank Junior Research Group, Key Laboratory of Cellular and Molecular Evolution, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming 650223, China
b Beijing Genomics Institute, Chinese Academy of Sciences, Beijing 101300, China
c Department of Biochemistry and Molecular Biology, University of Southern Denmark, DK-5230, Odense M, Denmark
d Department of Ecology and Evolution, University of Chicago, Chicago 60637, Illinois
e Key Laboratory of Plant Stress Research, College of Life Science, Shandong Normal University, Jinan 250014, China
f Graduate School of Chinese Academy Sciences, Beijing 100039, China
g Institute of Human Genetics, University of Aarhus, DK-8000, Aarhus C, Denmark
2 To whom correspondence should be addressed. E-mail mlong{at}uchicago.edu or wangj{at}genomics.org.cn; fax 773-702-9740.
Retroposition is widely found to play essential roles in origination of new mammalian and other animal genes. However, the scarcity of retrogenes in plants has led to the assumption that plant genomes rarely evolve new gene duplicates by retroposition, despite abundant retrotransposons in plants and a reported long terminal repeat (LTR) retrotransposon-mediated mechanism of retroposing cellular genes in maize (Zea mays). We show extensive retropositions in the rice (Oryza sativa) genome, with 1235 identified primary retrogenes. We identified 27 of these primary retrogenes within LTR retrotransposons, confirming a previously observed role of retroelements in generating plant retrogenes. Substitution analyses revealed that the vast majority are subject to negative selection, suggesting, along with expression data and evidence of age, that they are likely functional retrogenes. In addition, 42% of these retrosequences have recruited new exons from flanking regions, generating a large number of chimerical genes. We also identified young chimerical genes, suggesting that gene origination through retroposition is ongoing, with a rate an order of magnitude higher than the rate in primates. Finally, we observed that retropositions have followed an unexpected spatial pattern in which functional retrogenes avoid centromeric regions, while retropseudogenes are randomly distributed. These observations suggest that retroposition is an important mechanism that governs gene evolution in rice and other grass species.
This article has been cited by other articles:

|
 |

|
 |
 
Z. Zhu, Y. Zhang, and M. Long
Extensive Structural Renovation of Retrogenes in the Evolution of the Populus Genome
Plant Physiology,
December 1, 2009;
151(4):
1943 - 1951.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
M. Matsuno,, V. Compagnon, G. A. Schoch, M. Schmitt, D. Debayle, J.-E. Bassard, B. Pollet, A. Hehn, D. Heintz, P. Ullmann, et al.
Evolution of a Novel Phenolic Pathway for Pollen Development
Science,
September 25, 2009;
325(5948):
1688 - 1692.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
C. Zou, M. D. Lehti-Shiu, F. Thibaud-Nissen, T. Prakash, C. R. Buell, and S.-H. Shiu
Evolutionary and Expression Signatures of Pseudogenes in Arabidopsis and Rice
Plant Physiology,
September 1, 2009;
151(1):
3 - 15.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
M. Fablet, M. Bueno, L. Potrzebowski, and H. Kaessmann
Evolutionary Origin and Functions of Retrogene Introns
Mol. Biol. Evol.,
September 1, 2009;
26(9):
2147 - 2156.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
L. Yang and J. L. Bennetzen
Structure-based discovery and description of plant and animal Helitrons
PNAS,
August 4, 2009;
106(31):
12832 - 12837.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
S.-Y. Jiang, A. Christoffels, R. Ramamoorthy, and S. Ramachandran
Expansion Mechanisms and Functional Annotations of Hypothetical Genes in the Rice Genome
Plant Physiology,
August 1, 2009;
150(4):
1997 - 2008.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
X. Cheng, D. Zhang, Z. Cheng, B. Keller, and H.-Q. Ling
A New Family of Ty1-copia-Like Retrotransposons Originated in the Tomato Genome by a Recent Horizontal Transfer Event
Genetics,
April 1, 2009;
181(4):
1183 - 1193.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
K. Hanada, V. Vallejo, K. Nobuta, R. K. Slotkin, D. Lisch, B. C. Meyers, S.-H. Shiu, and N. Jiang
The Functional Role of Pack-MULEs in Rice Inferred from Purifying Selection and Expression Profile
PLANT CELL,
January 1, 2009;
21(1):
25 - 38.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
R. L. Rogers, T. Bedford, and D. L. Hartl
Formation and Longevity of Chimeric and Duplicate Genes in Drosophila melanogaster
Genetics,
January 1, 2009;
181(1):
313 - 322.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
A. Wawrzynski, T. Ashfield, N. W.G. Chen, J. Mammadov, A. Nguyen, R. Podicheti, S. B. Cannon, V. Thareau, C. Ameline-Torregrosa, E. Cannon, et al.
Replication of Nonautonomous Retroelements in Soybean Appears to Be Both Recent and Common
Plant Physiology,
December 1, 2008;
148(4):
1760 - 1771.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
S. D. Russell, P. L. Bhalla, and M. B. Singh
Transcriptome-Based Examination of Putative Pollen Allergens of Rice (Oryza sativa ssp. japonica)
Mol Plant,
September 1, 2008;
1(5):
751 - 759.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
C. Fan, Y. Zhang, Y. Yu, S. Rounsley, M. Long, and R. A. Wing
The Subtelomere of Oryza sativa Chromosome 3 Short Arm as a Hot Bed of New Gene Origination in Rice
Mol Plant,
September 1, 2008;
1(5):
839 - 850.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
Q. Zhou, G. Zhang, Y. Zhang, S. Xu, R. Zhao, Z. Zhan, X. Li, Y. Ding, S. Yang, and W. Wang
On the origin of new genes in Drosophila
Genome Res.,
September 1, 2008;
18(9):
1446 - 1455.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
H. Dai, Y. Chen, S. Chen, Q. Mao, D. Kennedy, P. Landback, A. Eyre-Walker, W. Du, and M. Long
The evolution of courtship behaviors through the origination of a new gene in Drosophila
PNAS,
May 27, 2008;
105(21):
7478 - 7483.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
B. S. Gaut and J. Ross-Ibarra
Selection on Major Components of Angiosperm Genomes
Science,
April 25, 2008;
320(5875):
484 - 486.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
P. H. Maxwell and M. J. Curcio
Retrosequence formation restructures the yeast genome
Genes & Dev.,
December 15, 2007;
21(24):
3308 - 3318.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
M.-S. Shiao, P. Khil, R. D. Camerini-Otero, T. Shiroishi, K. Moriwaki, H.-T. Yu, and M. Long
Origins of New Male Germ-line Functions from X-Derived Autosomal Retrogenes in the Mouse
Mol. Biol. Evol.,
October 1, 2007;
24(10):
2242 - 2253.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
H. Zheng, J. Shi, X. Fang, Y. Li, S. Vang, W. Fan, J. Wang, Z. Zhang, W. Wang, K. Kristiansen, et al.
FGF: A web tool for Fishing Gene Family in a whole genome database
Nucleic Acids Res.,
July 13, 2007;
35(suppl_2):
W121 - W125.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
B. Xue, A. P. Rooney, M. Kajikawa, N. Okada, and W. L. Roelofs
Novel sex pheromone desaturases in the genomes of corn borers generated through gene duplication and retroposon fusion
PNAS,
March 13, 2007;
104(11):
4467 - 4472.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
H. Chen, V. J. Karplus, H. Ma, and X. W. Deng
Plant Biology Research Comes of Age in China
PLANT CELL,
November 1, 2006;
18(11):
2855 - 2864.
[Full Text]
[PDF]
|
 |
|
|
|