TY - JOUR
T1 - The mouse DNA binding protein Rc for the kappa B motif of transcription and for the V(D)J recombination signal sequences contains composite DNA- protein interaction domains and belongs to a new family of large transcriptional proteins
AU - Wu, Lai Chu
AU - Liu, Yiling
AU - Strandtmann, J.
AU - Mak, Chi Ho
AU - Lee, Bo
AU - Li, Zhiling
AU - Yu, C. Yung
N1 - Funding Information:
We are indebted to Dr. Terry Rabbitts (MRC Laboratory of Molecular Biology, Cambridge, UK) and Dr. Ron Whisler for support and Dr. David Baltimore (Rockefeller University, NY) for gifts of the 22D6 cell line and cDNA library. This research was supported by Grant GM48798 (L.C.W.) from the National Institutes of Health and in part by Pittsburgh Supercomputing Center Grant MCB940021P from the NIH National Center for Research Resource.
PY - 1996/8/1
Y1 - 1996/8/1
N2 - Rc is a DNA binding protein with dual specificities for the V(D)J recombination signal sequences and for the B motif of the immunoglobulin kappa chain gene enhancer. The largest Rc transcript present in lymphoid cells/tissues is ~9 kb. Molecular cloning and sequence determination for 8822 bp of mouse Rc cDNA revealed an open reading frame of 2282 amino acids and long 5'- and 3'-untranslated regions. The derived amino acid sequence contains multiple DNA and protein interaction domains. Composite ZAS structures with tandem zinc fingers, an acidic motif, and a Ser/Thr-rich segment are located near the N-terminal and the C-terminal regions. The middle region of Rc contains a lone zinc finger, an acidic motif, a Ser-rich region, a nucleus localization signal, and GTPase motifs. Cloning and characterization of a mouse Rc gene show that the Rc cDNA corresponds to seven exons located in a genomic region spanning 70 kb. Exon 2 is exceptionally large, with 5487 bp. cDNA cloning and Northern blot analyses revealed multiple Rc transcripts, probably generated by alternative splicings. Sequence comparisons show that Rc belongs to a ZAS protein family that is involved in gene transcription and/or DNA recombination. The major histocompatibility complex class I gene enhancer binding proteins MBP1 and MBP2 are other representatives of this ZAS protein family.
AB - Rc is a DNA binding protein with dual specificities for the V(D)J recombination signal sequences and for the B motif of the immunoglobulin kappa chain gene enhancer. The largest Rc transcript present in lymphoid cells/tissues is ~9 kb. Molecular cloning and sequence determination for 8822 bp of mouse Rc cDNA revealed an open reading frame of 2282 amino acids and long 5'- and 3'-untranslated regions. The derived amino acid sequence contains multiple DNA and protein interaction domains. Composite ZAS structures with tandem zinc fingers, an acidic motif, and a Ser/Thr-rich segment are located near the N-terminal and the C-terminal regions. The middle region of Rc contains a lone zinc finger, an acidic motif, a Ser-rich region, a nucleus localization signal, and GTPase motifs. Cloning and characterization of a mouse Rc gene show that the Rc cDNA corresponds to seven exons located in a genomic region spanning 70 kb. Exon 2 is exceptionally large, with 5487 bp. cDNA cloning and Northern blot analyses revealed multiple Rc transcripts, probably generated by alternative splicings. Sequence comparisons show that Rc belongs to a ZAS protein family that is involved in gene transcription and/or DNA recombination. The major histocompatibility complex class I gene enhancer binding proteins MBP1 and MBP2 are other representatives of this ZAS protein family.
UR - https://www.scopus.com/pages/publications/0030219846
U2 - 10.1006/geno.1996.0380
DO - 10.1006/geno.1996.0380
M3 - Article
C2 - 8812474
AN - SCOPUS:0030219846
SN - 0888-7543
VL - 35
SP - 415
EP - 424
JO - Genomics
JF - Genomics
IS - 3
ER -