Concerted Evolution of the Tandemly Repeated Genes Encoding Human U2 SnRNA (the RNU2 Locus) Involves Rapid Intrachromosomal Homogenization and Rare Interchromosomal Gene Conversion

Overview

Journal EMBO J

Specialties Biotechnology
Molecular Biology

Date 1997 Feb 3

PMID 9034341

Citations 40

Authors

D Liao

T Pavelitz

J R Kidd

K K Kidd

A M Weiner

Affiliations

Soon will be listed here.

Abstract

We have surveyed the tandemly repeated genes encoding U2 snRNA in a diverse panel of humans. We found only two polymorphisms within the U2 repeat unit: a SacI polymorphism (alleles SacI+ or SacI-) and a CT microsatellite polymorphism (alleles CT+ or CT-). Surprisingly, individual U2 tandem arrays are entirely SacI+ or SacI-, and entirely CT+ or CT-, although the SacI and CT alleles can occur in any combination. We also found that polymorphisms in the left and right junction regions flanking the tandem array fall into only two haplotypes (JL+ and JL-, JR+ and JR-). Most surprisingly, JL+ is always associated with JR+, and JL- with JR-. Thus individual U2 arrays do not exchange flanking markers, despite independent assortment and subsequent homogenization of the SacI and CT alleles within the U2 repeat units. We propose that the primary driving force for concerted evolution of the tandem U2 genes is intrachromosomal homogenization; interchromosomal genetic exchanges are much rarer, and reciprocal nonsister chromatid exchange apparently does not occur. Thus concerted evolution of the U2 tandem array occurs in situ along a chromosome lineage, and linkage disequilibrium between sequences flanking the U2 array may persist for long periods of time.

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