Emergence of primate genes by retrotransposon-mediated sequence transduction
- Jinchuan Xing†,
- Hui Wang†,
- Victoria P. Belancio‡,
- Richard Cordaux†,
- Prescott L. Deininger‡, and
- Mark A. Batzer†,§
- †Department of Biological Sciences, Biological Computation and Visualization Center, Center for BioModular Multi-Scale Systems, Louisiana State University, 202 Life Sciences Building, Baton Rouge, LA 70803; and
- ‡Tulane Cancer Center SL-66, Department of Environmental Health Sciences, Tulane University Health Sciences Center, New Orleans, LA 70112
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Edited by Susan R. Wessler, University of Georgia, Athens, GA, and approved June 28, 2006 (received for review April 20, 2006)
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Fig. 1.Identification of SVA 3′ transduction events and their source elements. Shown are the schematic diagrams for the identification process. Flanking sequences of the source locus are shown as blue boxes; TSDs are shown as yellow and green arrows. SVA elements are depicted as red bars, and the transduced sequences are shown as blue bars and labeled “TD.” SVA element poly(A) tails are shown as “(AAA)n.” The numbers in parentheses correspond to the total number of SVA elements/groups identified in each step.
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Fig. 2.Length distribution of 3′ transduction events. The number of human SVA-mediated 3′ transduction events in each 100-bp size interval is shown.
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Fig. 3.SVA 3′ transduction events. One group of SVA 3′ transduction events (H3_186) is shown. Flanking sequences of the original locus are shown as blue boxes, and the flanking sequences of the transduced loci are shown as light blue boxes. TSDs are shown as yellow and green arrows. SVA elements are depicted as red bars, and the transduced sequences are shown as blue bars and labeled “TD.” SVA element poly(A) tails are shown as “(AAA)n.”
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Fig. 4.SVA transduction-mediated gene duplication. (A) Schematic diagram of the H17_76 transduction group in the human genome. Flanking sequences of the original locus are shown as blue boxes, and the flanking sequences of the transduced loci are shown as light blue boxes. TSDs are shown as yellow and green arrows. SVA elements are depicted as red bars, the transduced sequences are shown as blue bars, and coding regions are shown as purple bars. SVA element poly(A) tails are shown as “(AAA)n.” (B) Schematic diagrams for putative evolutionary scenarios of the SVA transduction-mediated gene duplications. Approximately 7 million to 14 million years ago, one active SVA element was inserted upstream of the original AMAC gene locus. Then, transcription of this active SVA element transduced the full-length AMAC gene sequence. During the retrotransposition process, the intron of the gene was removed by RNA processing machinery. Finally, the SVA element along with the intronless AMAC gene sequence retrotransposed into new genomic locations. The original retrotransposition-competent SVA element upstream of the source locus was eventually lost in the population. The predicted RNA transcripts are shown as curved lines. (C) The phylogenetic relationships among various species used in dN/dS analysis.
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Fig. 5.Expression analysis of AMAC gene duplicates in humans. (A) Agarose gel chromatograph of RT-PCR products derived from human testis (T) and placental (P) RNA templates. Negative controls with no reverse transcriptase (RT −) are on the left, a 100-bp marker (M) is in the middle, and reactions with reverse transcriptase (RT +) are on the right; the sizes of the correct fragments are indicated. (B) Relative expression levels of four human AMAC gene duplicates in human testis and placenta. Human genomic DNA (HeLa) amplification is the control for uniform amplification of all gene duplicates.
Footnotes
- §To whom correspondence should be addressed. E-mail: mbatzer{at}lsu.edu
- © 2006 by The National Academy of Sciences of the USA
