Alu insertion polymorphisms for the study of human genomic diversity

Astrid M. Roy-Engel, Tulane University School of Public Health and Tropical Medicine
Marion L. Carroll, LSUHSC School of Medicine
Erika Vogel, Tulane University School of Public Health and Tropical Medicine
Randall K. Garber, LSUHSC School of Medicine
Son V. Nguyen, LSUHSC School of Medicine
Abdel Halim Salem, LSUHSC School of Medicine
Mark A. Batzer, LSUHSC School of Medicine
Prescott L. Deininger, Tulane University School of Public Health and Tropical Medicine

Abstract

Genomic database mining has been a very useful aid in the identification and retrieval of recently integrated Alu elements from the human genome. We analyzed Alu elements retrieved from the GenBank database and identified two new Alu subfamilies, Alu Yb9 and Alu Yc2, and further characterized Yc1 subfamily members. Some members of each of the three subfamilies have inserted in the human genome so recently that about a one-third of the analyzed elements are polymorphic for the presence/absence of the Alu repeat in diverse human populations. These newly identified Alu insertion polymorphisms will serve as identical-by-descent genetic markers for the study of human evolution and forensics. Three previously classified Alu Y elements linked with disease belong to the Yc1 subfamily, supporting the retroposition potential of this subfamily and demonstrating that the Alu Y subfamily currently has a very low amplification rate in the human genome.