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The left-right determinant inversin has highly conserved ankyrin repeat and IQ domains and interacts with calmodulin

The left-right determinant inversin has highly conserved ankyrin repeat and IQ domains and interacts with calmodulin
The left-right determinant inversin has highly conserved ankyrin repeat and IQ domains and interacts with calmodulin
All vertebrates have a left-right body axis with invariant asymmetries of the heart and the positions of the abdominal viscera. Major advances have recently been made in defining molecular components of the pathway specifying the vertebrate left-right axis, but our knowledge of the early determinants is extremely limited. In the inv mouse the left-right axis is consistently reversed, unlike other vertebrate mutants where randomisation of situs is apparent. The gene disrupted in this mouse encodes a 1062-amino-acid protein, inversin. We previously reported 16 tandem ankyrin repeats, spanning amino acids 13-557, and two putative nuclear localisation sequences, but otherwise the sequence offered few clues to the possible function. In order to identify regions likely to be functionally important, we have identified and characterised orthologous sequences in several species, including chick, Xenopus and zebrafish. Sequence comparisons show strong conservation of the ankyrin repeat region and also a lysine-rich domain spanning amino acids 558-604. Further analysis identified a highly conserved IQ calmodulin-binding domain in the latter region and another such domain in an otherwise poorly conserved C-terminal region. A yeast two-hybrid screen identified calmodulin in one third of the positive clones, and we confirmed this interaction by immunoprecipitation.
0340-6717
377-384
Morgan, David
7eaba985-9217-4b5a-9d33-0f2caf51b4e1
Goodship, Judith
14bfb2d1-f436-44f1-bee2-e91ee73dd1c4
Essner, Jeffrey J.
70ab5c80-33a1-4f56-8f5d-2f5ee100de4c
Vogan, Kyle J.
9edfce17-7a2c-4dbd-99ef-195181bc4e54
Turnpenny, Lee
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Yost, Joseph H.
77a40878-6932-4e87-bdb6-fc7d73ae5fb1
Tabin, Clifford J.
b56d0023-7e1e-4a26-9179-128269bc983a
Strachan, Tom
9ab590c0-9f84-43f4-8bf3-0946c7925594
Morgan, David
7eaba985-9217-4b5a-9d33-0f2caf51b4e1
Goodship, Judith
14bfb2d1-f436-44f1-bee2-e91ee73dd1c4
Essner, Jeffrey J.
70ab5c80-33a1-4f56-8f5d-2f5ee100de4c
Vogan, Kyle J.
9edfce17-7a2c-4dbd-99ef-195181bc4e54
Turnpenny, Lee
31a2fb0f-b76a-490a-845d-f9d9a1501d3d
Yost, Joseph H.
77a40878-6932-4e87-bdb6-fc7d73ae5fb1
Tabin, Clifford J.
b56d0023-7e1e-4a26-9179-128269bc983a
Strachan, Tom
9ab590c0-9f84-43f4-8bf3-0946c7925594

Morgan, David, Goodship, Judith, Essner, Jeffrey J., Vogan, Kyle J., Turnpenny, Lee, Yost, Joseph H., Tabin, Clifford J. and Strachan, Tom (2002) The left-right determinant inversin has highly conserved ankyrin repeat and IQ domains and interacts with calmodulin. Human Genetics, 110 (4), 377-384. (doi:10.1007/s00439-002-0696-4).

Record type: Article

Abstract

All vertebrates have a left-right body axis with invariant asymmetries of the heart and the positions of the abdominal viscera. Major advances have recently been made in defining molecular components of the pathway specifying the vertebrate left-right axis, but our knowledge of the early determinants is extremely limited. In the inv mouse the left-right axis is consistently reversed, unlike other vertebrate mutants where randomisation of situs is apparent. The gene disrupted in this mouse encodes a 1062-amino-acid protein, inversin. We previously reported 16 tandem ankyrin repeats, spanning amino acids 13-557, and two putative nuclear localisation sequences, but otherwise the sequence offered few clues to the possible function. In order to identify regions likely to be functionally important, we have identified and characterised orthologous sequences in several species, including chick, Xenopus and zebrafish. Sequence comparisons show strong conservation of the ankyrin repeat region and also a lysine-rich domain spanning amino acids 558-604. Further analysis identified a highly conserved IQ calmodulin-binding domain in the latter region and another such domain in an otherwise poorly conserved C-terminal region. A yeast two-hybrid screen identified calmodulin in one third of the positive clones, and we confirmed this interaction by immunoprecipitation.

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Published date: 2002

Identifiers

Local EPrints ID: 24871
URI: http://eprints.soton.ac.uk/id/eprint/24871
ISSN: 0340-6717
PURE UUID: 1d7aac90-77a4-47f5-804a-3ddb5abcadba

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Date deposited: 05 Apr 2006
Last modified: 15 Mar 2024 06:59

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Contributors

Author: David Morgan
Author: Judith Goodship
Author: Jeffrey J. Essner
Author: Kyle J. Vogan
Author: Lee Turnpenny
Author: Joseph H. Yost
Author: Clifford J. Tabin
Author: Tom Strachan

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