Expression of tandem gene duplicates is often greater than twofold

Tandem gene duplication is an important mutational process in evolutionary adaptation and human disease. Hypothetically, two tandem gene copies should produce twice the output of a single gene, but this expectation has not been rigorously investigated. Here, we show that tandem duplication often results in more than double the gene activity. A naturally occurring tandem duplication of the Alcohol dehydrogenase (Adh) gene exhibits 2.6-fold greater expression than the single-copy gene in transgenic Drosophila This tandem duplication also exhibits greater activity than two copies of the gene in trans, demonstrating that it is the tandem arrangement and not copy number that is the cause of overactivity. We also show that tandem duplication of an unrelated synthetic reporter gene is overactive (2.3- to 5.1-fold) at all sites in the genome that we tested, suggesting that overactivity could be a general property of tandem gene duplicates. Overactivity occurs at the level of RNA transcription, and therefore tandem duplicate overactivity appears to be a previously unidentified form of position effect. The increment of surplus gene expression observed is comparable to many regulatory mutations fixed in nature and, if typical of other genomes, would shape the fate of tandem duplicates in evolution.

Medienart:

E-Artikel

Erscheinungsjahr:

2016

Erschienen:

2016

Enthalten in:

Zur Gesamtaufnahme - volume:113

Enthalten in:

Proceedings of the National Academy of Sciences of the United States of America - 113(2016), 21 vom: 24. Mai, Seite 5988-92

Sprache:

Englisch

Beteiligte Personen:

Loehlin, David W [VerfasserIn]
Carroll, Sean B [VerfasserIn]

Links:

Volltext

Themen:

ADH protein, Drosophila
Alcohol Dehydrogenase
Drosophila Proteins
EC 1.1.1.1
Gene expression
Gene structure
Genome evolution
Journal Article
Position effect
Research Support, Non-U.S. Gov't
Tandem duplication

Anmerkungen:

Date Completed 22.12.2016

Date Revised 11.01.2019

published: Print-Electronic

GENBANK: KU559568

Citation Status MEDLINE

doi:

10.1073/pnas.1605886113

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM260191175