The Sox-13 gene: Structure, promoter characterization, and chromosomal localization

Genomics

Volumn 57, Issue 2, 1999, Pages 301-305

  Roose, Jeroen ^a   Korver, Wouter ^a   De Boer, Rosalie ^a   Kuipers, Jeroen ^a   Hurenkamp, Jolanda ^a   Clevers, Hans ^a  

^a UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

TRANSCRIPTION FACTOR;

ARTICLE; CHROMOSOMAL LOCALIZATION; CHROMOSOME 1Q; DNA LIBRARY; EXON; FLUORESCENCE IN SITU HYBRIDIZATION; GENE STRUCTURE; GENETIC ANALYSIS; INTRON; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROMOTER REGION; SEQUENCE ANALYSIS; SEQUENCE HOMOLOGY; TRANSCRIPTION INITIATION; TRANSCRIPTION REGULATION;

MAMMALIA; MURINAE; RODENTIA;

EID: 0345620819     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1999.5779     Document Type: Article

References (24)

1. Clepet C., Schafer A., Sinclair A., Palmer M., Lovell Badge R., Goodfellow P. The human SRY transcript. Hum. Mol. Genet. 2:1993;2007-2012.
2. Collignon J., Sockanathan S., Hacker A., Cohen Tannoudji M., Norris D., Rastan S., Stevanovic M., Goodfellow P., Lovell Badge R. A comparison of the properties of Sox-3 with Sry and two related genes, Sox-1 and Sox-2. Development. 122:1996;509-520.
3. Connor F., Wright E., Denny P., Koopman P., Ashworth A. The Sry-related HMG box-containing gene Sox6 is expressed in the adult testis and developing nervous system of the mouse. Nucleic Acids Res. 23:1995;3365-3372.
4. Durand J. B., Bachinski L. L., Bieling L. C., Czernuszewicz G. Z., Abchee A. B., Yu Q. T., Tapscott T., Hill R., Ifegwu J., Marian A. J. Localization of a gene responsible for familial dilated cardiomyopathy to chromosome 1q32. Circulation. 92:1995;3387-3389.
5. Foster J., Dominguez-Steglich A., Guioli S., Kwok C., Weller P., Stevanovic M., Weissenbach J., Mansour S., Young I., Goodfellow P. Campomelic dysplasia and autosomal sex reversal caused by mutations in anSRY. Nature. 372:1994;525-530.
6. Goodfellow P., Lovell Badge R. SRY and sex determination in mammals. Annu. Rev. Genet. 27:1993;71-92.
7. Hacker A., Capel B., Goodfellow P., Lovell Badge R. Expression of Sry, the mouse sex determining gene. Development. 121:1995;1603-1614.
8. Jay P., Goze C., Marsollier C., Taviaux S., Hardelin J., Koopman P., Berta P. The human SOX11 gene: Cloning, chromosomal assignment, and tissue expression. Genomics. 29:1995;541-545.
9. Jay P., Iman Sahly, Goze C., Taviaux S., Poulat F., Couly G., Abitbol M., Berta P. SOX22 is a new member of the SOX gene family, mainly expressed in human nervous tissue. Hum. Mol. Genet. 6:1997;1069-1077.
10. Kanai Y., Kanai Azuma M., Noce T., Saido T., Shiroishi T., Hayashi Y., Yazaki K. Identification of two Sox17 messenger RNA isoforms, with and without the high mobility group box region, and their differential expression in mouse spermatogenesis. J. Cell Biol. 133:1996;667.
11. Mitelman F. Catalog of Chromosome Aberrations in Cancer. 1994;Wiley-Liss, New York.
12. Pevny H. P., Lovell-Badge R. Sox genes find their feed. Curr. Opin. Genet. Dev. 7:1997;338-344.
13. Pingault V., Bondurand N., Kuhlbrodt K., Goerich D., Prehu M., Puliti A., Herbarth B., Hermans-Borgmeyer I., Legius E., Matthijs G. Sox-10. Nat. Genet. 18:1998;171-173.
14. Pinkel D., Straume T., Gray J. Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization. Proc. Natl. Acad. Sci. USA. 83:1986;2934-2938.
15. Roose J., Korver W., Oving E., Wilson A., Wagenaar G., Markman M., Lamers W., Clevers H. High expression of the HMG box factor Sox-13 in arterial walls during embryonic development. Nucleic Acids Res. 26:1998;469-476.
16. Roose J., Molenaar M., Peterson J., Hurenkamp J., Brantjes H., Moerer P., van de Wetering M., Destree O., Clevers H. TheXenopus. Nature. 395:1998;608-612.
17. Sander A., Schmelzle R., Murray J. Evidence for a microdeletion in 1q32-41 involving the gene responsible for Van der Woude syndrome. Hum. Mol. Genet. 3:1994;575-578.
18. Schilham M., Oosterwegel M., Moerer P., Ya J., de Boer P., van de Wetering M., Verbeek S., Lamers W., Kruisbeek A., Cumano A. et al. Defects in cardiac outflow tract formation and pro-B-lymphocyte expansion in mice lacking Sox-4. Nature. 380:1996;711-714.
19. Schilham M., van Eijk M., van de Wetering M., Clevers H. The murine Sox-4 protein is encoded on a single exon. Nucleic Acids Res. 21:1993;2009.
20. Takamatsu N., Kanda H., Tsuchiya I., Yamada S., Ito M., Kabeno S., Shiba T., Yamashita S. A gene that is related to SRY and is expressed in the testes encodes a leucine zipper-containing protein. Mol. Cell. Biol. 15:1995;3759-3766.
21. Wagner T., Wirth J., Meyer J., Zabel B., Held M., Zimmer J., Pasantes J., Bricarelli F., Keutel J., Hustert E. Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9. Cell. 79:1994;1111-1120.
22. Wright E., Hargrave M. R., Christiansen J., Cooper L., Kun J., Evans T., Gangadharan U., Greenfield A., Koopman P. The Sry-related gene Sox9 is expressed during chondrogenesis in mouse embryos. Nat. Genet. 9:1995;15-20.
23. Wunderle V., Critcher R., Ashworth A., Goodfellow P. Cloning and characterization of SOX5, a new member of the human SOX gene family. Genomics. 36:1996;354-358.
24. Yamashita A., Suzuki S., Fujitani K., Kojima M., Kanda H., Ito M., Takamatsu N., Yamashita S., Shiba T. cDNA cloning of a novel rainbow trout SRY-type HMG box protein, rtSox23, and its functional analysis. Gene. 209:1998;193-200.