Functional equivalency of amphioxus and vertebrate Pax258 transcription factors suggests that the activation of mid-hindbrain specific genes in vertebrates occurs via the recruitment of Pax regulatory elements.
暂无分享,去创建一个
Michael Schubert | V. Beneš | Z. Kozmík | L. Holland | C. Burgtorf | M. Schubert | Zbynek Kozmik | Carola Burgtorf | Linda Z Holland | Vladimír Benes | Jana Krelová | Jana Krelová
[1] R. Balling,et al. Pax genes and organogenesis , 1997, BioEssays : news and reviews in molecular, cellular and developmental biology.
[2] G. Jiménez,et al. Transcriptional repression by Pax5 (BSAP) through interaction with corepressors of the Groucho family , 2000, The EMBO journal.
[3] A. Aguzzi,et al. Pax-5 encodes the transcription factor BSAP and is expressed in B lymphocytes, the developing CNS, and adult testis. , 1992, Genes & development.
[4] A. Barberis,et al. A novel B-cell lineage-specific transcription factor present at early but not late stages of differentiation. , 1990, Genes & development.
[5] J. Pačes,et al. Characterization of an amphioxus paired box gene, AmphiPax2/5/8: developmental expression patterns in optic support cells, nephridium, thyroid-like structures and pharyngeal gill slits, but not in the midbrain-hindbrain boundary region. , 1999, Development.
[6] G. Halder,et al. twin of eyeless, a second Pax-6 gene of Drosophila, acts upstream of eyeless in the control of eye development. , 1999, Molecular cell.
[7] P. Gruss,et al. Conserved biological function between Pax-2 and Pax-5 in midbrain and cerebellum development: evidence from targeted mutations. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[8] M. Busslinger,et al. The promoter of the CD19 gene is a target for the B-cell-specific transcription factor BSAP , 1992, Molecular and cellular biology.
[9] J A Epstein,et al. Two independent and interactive DNA-binding subdomains of the Pax6 paired domain are regulated by alternative splicing. , 1994, Genes & development.
[10] G. Schaffner,et al. DNA sequence recognition by Pax proteins: bipartite structure of the paired domain and its binding site. , 1993, Genes & development.
[11] M. Busslinger,et al. DNA-binding and transactivation properties of Pax-6: three amino acids in the paired domain are responsible for the different sequence recognition of Pax-6 and BSAP (Pax-5) , 1995, Molecular and cellular biology.
[12] H. Lehrach,et al. Characterization of amphioxus AmphiWnt8 : insights into the evolution of patterning of the embryonic dorsoventral axis , 2000, Evolution & development.
[13] M. Brand,et al. A series of no isthmus (noi) alleles of the zebrafish pax2.1 gene reveals multiple signaling events in development of the midbrain-hindbrain boundary. , 1998, Development.
[14] G. Superti-Furga,et al. Developmental and tissue-specific regulation of a novel transcription factor of the sea urchin. , 1989, Genes & development.
[15] A. Joyner,et al. Two Pax2/5/8-binding sites in Engrailed2 are required for proper initiation of endogenous mid-hindbrain expression , 2000, Mechanisms of Development.
[16] M. Busslinger,et al. The characterization of novel Pax genes of the sea urchin and Drosophila reveal an ancient evolutionary origin of the Pax2/5/8 subfamily , 1997, Mechanisms of Development.
[17] M. Busslinger,et al. Alternatively spliced insertions in the paired domain restrict the DNA sequence specificity of Pax6 and Pax8 , 1997, The EMBO journal.
[18] K. Vogan,et al. An alternative splicing event in the Pax-3 paired domain identifies the linker region as a key determinant of paired domain DNA-binding activity , 1996, Molecular and cellular biology.
[19] C. Desplan,et al. The paired box encodes a second DNA-binding domain in the paired homeo domain protein. , 1991, Genes & development.
[20] Multiple bandshift assay: rapid identification and cloning of DNA fragments containing specific protein-binding sites. , 1990, Gene.
[21] H. Gee. Return of the amphioxus , 1994, Nature.
[22] S. Krauss,et al. Zebrafish Pax9 Encodes Two Proteins with Distinct C-terminal Transactivating Domains of Different Potency Negatively Regulated by Adjacent N-terminal Sequences* , 1996, The Journal of Biological Chemistry.
[23] L. Holland,et al. Characterization of an amphioxus Wnt gene, AmphiWnt11, with possible roles in myogenesis and tail outgrowth , 2000, Genesis.
[24] L. Holland,et al. Developmental expression of AmphiWnt1, an amphioxus gene in the Wnt1/wingless subfamily , 2000, Development Genes and Evolution.
[25] P. Gruss,et al. Pax genes and their role in organogenesis. , 1999, Cancer research.
[26] L. Holland,et al. Characterization of two amphioxus Wnt genes (AmphiWnt4 and AmphiWnt7b) with early expression in the developing central nervous system , 2000, Developmental dynamics : an official publication of the American Association of Anatomists.
[27] Stephen W. Wilson,et al. Zebrafish pax[b] is involved in the formation of the midbrain–hindbrain boundary , 1992, Nature.
[28] N. Williams,et al. Sequence and embryonic expression of the amphioxus engrailed gene (AmphiEn): the metameric pattern of transcription resembles that of its segment-polarity homolog in Drosophila. , 1997, Development.
[29] M. Busslinger,et al. C‐terminal activating and inhibitory domains determine the transactivation potential of BSAP (Pax‐5), Pax‐2 and Pax‐8. , 1996, The EMBO journal.
[30] A. Joyner,et al. Two Pax-binding sites are required for early embryonic brain expression of an Engrailed-2 transgene. , 1996, Development.