Cloning of inv, a gene that controls left/right asymmetry and kidney development

Most vertebrate internal organs show a distinctive left/right asymmetry. The inv (inversion of embryonic turning) mutation in mice was created previously by random insertional mutagenesis; it produces both a constant reversal of left/right polarity (situs inversus) and cyst formation in the kidneys. Asymmetric expression patterns of the genes nodal and lefty are reversed in the inv mutant, indicating that inv may act early in left/right determination. Here we identify a new gene located at the inv locus. The encoded protein contains 15 consecutive repeats of an Ank/Swi6 motif, at its amino terminus. Expression of the gene is the highest in the kidneys and liver among adult tissues, and is seen in presomite-stage embryos. Analysis of the transgenic genome and the structure of the candidate gene indicate that the candidate gene is the only gene that is disrupted in inv mutants. Transgenic introduction of a minigene encoding the candidate protein restores normal left/right asymmetry and kidney development in the inv mutant, confirming the identity of the candidate gene.

[1]  Samuel E. Lux,et al.  Analysis of cDNA for human erythrocyte ankyrin indicates a repeated structure with homology to tissue-differentiation and cell-cycle control proteins , 1990, Nature.

[2]  H. Niwa,et al.  Efficient selection for high-expression transfectants with a novel eukaryotic vector. , 1991, Gene.

[3]  A. Klar A model for specification of the left-right axis in vertebrates. , 1994, Trends in genetics : TIG.

[4]  Y. Saijoh,et al.  Left–right asymmetric expression of the TGFβ-family member lefty in mouse embryos , 1996, Nature.

[5]  C. Tabin,et al.  A molecular pathway determining left-right asymmetry in chick embryogenesis , 1995, Cell.

[6]  S. Kuhara,et al.  Two closely‐related left‐right asymmetrically expressed genes, lefty‐1 and lefty‐2: their distinct expression domains, chromosomal linkage and direct neuralizing activity in Xenopus embryos , 1997, Genes to cells : devoted to molecular & cellular mechanisms.

[7]  B. Kwon,et al.  Conserved cysteine to serine mutation in tyrosinase is responsible for the classical albino mutation in laboratory mice. , 1990, Nucleic acids research.

[8]  A. Monaco,et al.  Yeast artificial chromosome libraries containing large inserts from mouse and human DNA. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[9]  W. M. Layton Random determination of a developmental process: reversal of normal visceral asymmetry in the mouse. , 1976, The Journal of heredity.

[10]  V. Bennett,et al.  Ankyrins. Adaptors between diverse plasma membrane proteins and the cytoplasm. , 1992, The Journal of biological chemistry.

[11]  Kathleen Weston,et al.  The Caenorhabditis elegans lin-12 gene encodes a transmembrane protein with overall similarity to Drosophila Notch , 1988, Nature.

[12]  J. Cooke,et al.  Control of Vertebrate Left-Right Asymmetry by a Snail-Related Zinc Finger Gene , 1997, Science.

[13]  Roger R. Markwald,et al.  Developmental mechanisms of heart disease , 1995 .

[14]  D. Wilkinson In situ hybridization: a practical approach , 1998 .

[15]  E. Blackburn,et al.  A novel DNA deletion-ligation reaction catalyzed in vitro by a developmentally controlled activity from tetrahymena cells , 1989, Cell.

[16]  J. Lawrence,et al.  Sensitive, high-resolution chromatin and chromosome mapping in situ: Presence and orientation of two closely integrated copies of EBV in a lymphoma line , 1988, Cell.

[17]  Yamamura Ken-ichi,et al.  Efficient selection for high-expression transfectants with a novel eukaryotic vector , 1991 .

[18]  H. Yost,et al.  Initiation of vertebrate left–right axis formation by maternal Vg1 , 1996, Nature.

[19]  H. Yost Regulation of vertebrate left–right asymmetries by extracellular matrix , 1992, Nature.

[20]  B. Hogan,et al.  Manipulating the mouse embryo: A laboratory manual , 1986 .

[21]  L. Peters,et al.  Ankyrins: structure and function in normal cells and hereditary spherocytes. , 1993, Seminars in hematology.

[22]  L. Breeden,et al.  Similarity between cell-cycle genes of budding yeast and fission yeast and the Notch gene of Drosophila , 1987, Nature.

[23]  K. Hummel,et al.  VISCERAL INVERSION AND ASSOCIATED ANOMALIES IN THE MOUSE , 1959 .

[24]  I. Greenwald,et al.  glp-1 and lin-12, genes implicated in distinct cell-cell interactions in C. elegans, encode similar transmembrane proteins , 1989, Cell.

[25]  H. Yost,et al.  The Left-Right Coordinator: The Role of Vg1 in Organizing Left-Right Axis Formation , 1998, Cell.

[26]  N. Copeland,et al.  Reversal of left-right asymmetry: a situs inversus mutation. , 1993, Science.

[27]  J. Collignon,et al.  Relationship between asymmetric nodal expression and the direction of embryonic turning , 1996, Nature.

[28]  D. Supp,et al.  Mutation of an axonemal dynein affects left–right asymmetry in inversus viscerum mice , 1997, Nature.

[29]  S. Aves,et al.  Cloning, sequencing and transcriptional control of the Schizosaccharomyces pombe cdc10 ‘start’ gene. , 1985, The EMBO journal.

[30]  Brenda J. Andrews,et al.  The yeast SWI4 protein contains a motif present in developmental regulators and is part of a complex involved in cell-cycle-dependent transcription , 1989, Nature.

[31]  D. Supp,et al.  Conserved left–right asymmetry of nodal expression and alterations in murine situs inversus , 1996, Nature.