Genomic structure and isoform expression of the mouse, rat and human Cbfa1/Osf2 transcription factor.

作者: Z.S Xiao , R Thomas , T.K Hinson , L.D Quarles

DOI: 10.1016/S0378-1119(98)00227-3

关键词:

摘要: Although the CBFA1 gene encodes an osteoblast-specific transcription factor that regulates osteoblast differentiation, uncertainty exists about organization of its 5' end and relevance a novel N-terminal sequence identified in mouse Cbfa1/Osf2 isoform. We found is encoded by previously unrecognized upstream exon, designated exon -1, which highly conserved mouse, rat human. In addition, two splice donor sites may be utilized to generate cDNAs containing different sequences. The first ATG site -1 predicted transcribe cDNA unique Osf2 sequence, whereas second gives rise contain sequences encoding 11 amino acid insert. human gene, additional 2-bp nucleotide insert shifts reading frame results stop codons derived from -1. 5'-most therefore, contains non-coding region rather than OSF2 homolog. absence homologous coding suggests not essential for functioning product. multiple transcripts single CBFA1/Cbfa1 were detected osteoblasts Northern analysis RT-PCR, including isoforms deletions exons 1 4. Thus, alternative use start splicing leads genesis with possible differences transactivation potentials.

参考文章(28)
Patrizio Castagnola, Massimo Gennari, Alessia Gaggero, Fabio Rossi, Antonio Daga, Maria Teresa Corsetti, Franco Calabi, Ranieri Cancedda, Expression of runtB is modulated during chondrocyte differentiation Experimental Cell Research. ,vol. 223, pp. 215- 226 ,(1996) , 10.1006/EXCR.1996.0075
Mee-Young Ahn, Suk-Chul Bae, Mitsuo Maruyama, Yoshiaki Ito, Comparison of the human genomic structure of the Runt domain-encoding PEBP2/CBFalpha gene family. Gene. ,vol. 168, pp. 279- 280 ,(1996) , 10.1016/0378-1119(95)00751-2
D. Levanon, V. Negreanu, Y. Bernstein, I. Bar-Am, L. Avivi, Y. Groner, AML1, AML2, and AML3, the Human Members of the runt domain Gene-Family: cDNA Structure, Expression, and Chromosomal Localization Genomics. ,vol. 23, pp. 425- 432 ,(1994) , 10.1006/GENO.1994.1519
Patricia Ducy, Rui Zhang, Valérie Geoffroy, Amy L Ridall, Gérard Karsenty, Osf2/Cbfa1: A Transcriptional Activator of Osteoblast Differentiation Cell. ,vol. 89, pp. 747- 754 ,(1997) , 10.1016/S0092-8674(00)80257-3
T Komori, H Yagi, S Nomura, A Yamaguchi, K Sasaki, K Deguchi, Y Shimizu, R.T Bronson, Y.-H Gao, M Inada, M Sato, R Okamoto, Y Kitamura, S Yoshiki, T Kishimoto, Targeted Disruption of Cbfa1 Results in a Complete Lack of Bone Formation owing to Maturational Arrest of Osteoblasts Cell. ,vol. 89, pp. 755- 764 ,(1997) , 10.1016/S0092-8674(00)80258-5
S Mundlos, F Otto, C Mundlos, J.B Mulliken, A.S Aylsworth, S Albright, D Lindhout, W.G Cole, W Henn, J.H.M Knoll, M.J Owen, R Mertelsmann, B.U Zabel, B.R Olsen, Mutations Involving the Transcription Factor CBFA1 Cause Cleidocranial Dysplasia Cell. ,vol. 89, pp. 773- 779 ,(1997) , 10.1016/S0092-8674(00)80260-3
Florian Otto, Anders P Thornell, Tessa Crompton, Angela Denzel, Kimberly C Gilmour, Ian R Rosewell, Gordon W.H Stamp, Rosa S.P Beddington, Stefan Mundlos, Bjorn R Olsen, Paul B Selby, Michael J Owen, Cbfa1, a Candidate Gene for Cleidocranial Dysplasia Syndrome, Is Essential for Osteoblast Differentiation and Bone Development Cell. ,vol. 89, pp. 765- 771 ,(1997) , 10.1016/S0092-8674(00)80259-7