auts2 Features and Expression Are Highly Conserved during Evolution Despite Different Evolutionary Fates Following Whole Genome Duplication
The gene plays major roles during brain development and is associated with various neuropathologies including autism. Data in non-mammalian species are scarce, and the aim of our study was to provide a comprehensive analysis of evolution in teleost fish, which are widely used for in vivo functional...
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Published in | Cells (Basel, Switzerland) Vol. 11; no. 17; p. 2694 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
MDPI AG
30.08.2022
MDPI |
Subjects | |
Online Access | Get full text |
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Summary: | The
gene plays major roles during brain development and is associated with various neuropathologies including autism. Data in non-mammalian species are scarce, and the aim of our study was to provide a comprehensive analysis of
evolution in teleost fish, which are widely used for in vivo functional analysis and biomedical purposes. Comparative genomics in 78 species showed that
and
originate from the teleost-specific whole genome duplication (TGD).
which is highly similar to human AUTS2, was almost systematically retained following TGD. In contrast,
which encodes for a shorter protein similar to a short human AUTS2 isoform, was lost more frequently and independently during evolution. RNA-seq analysis in 10 species revealed a highly conserved profile with predominant expression of both genes in the embryo, brain, and gonads. Based on protein length, conserved domains, and expression profiles, we speculate that the long human isoform functions were retained by
, while the short isoform functions were retained by
and/or
, depending on the lineage/species.
showed a burst in expression during medaka brain formation, where it was expressed in areas of the brain associated with neurodevelopmental disorders. Together, our data suggest a strong conservation of
functions in vertebrates despite different evolutionary scenarios in teleosts. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 These authors contributed equally to this work. |
ISSN: | 2073-4409 2073-4409 |
DOI: | 10.3390/cells11172694 |