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Summary Anatomy Item Literature (6354) Expression Attributions Wiki
XB-ANAT-254

Papers associated with oocyte (and gtf3a)

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Differential binding of zinc fingers from Xenopus TFIIIA and p43 to 5S RNA and the 5S RNA gene., Darby MK., Mol Cell Biol. July 1, 1992; 12 (7): 3155-64.

Interaction of Xenopus TFIIIC with the TFIIIA.5 S RNA gene complex., Keller HJ., J Biol Chem. September 5, 1992; 267 (25): 18190-8.

Comparison of the sequence and structure of transcription factor IIIA from Bufo americanus and Rana pipiens., Gaskins CJ., Gene. October 21, 1992; 120 (2): 197-206.

Identification of nuclear factors which interact with the 5' flanking region of the EF-1 alpha O gene in Xenopus laevis., Olesen OF., FEBS Lett. November 30, 1992; 313 (3): 205-9.

Role of TFIIIA zinc fingers in vivo: analysis of single-finger function in developing Xenopus embryos., Rollins MB., Mol Cell Biol. August 1, 1993; 13 (8): 4776-83.

Masking mRNA from translation in somatic cells., Ranjan M., Genes Dev. September 1, 1993; 7 (9): 1725-36.

Proteolytic footprinting of transcription factor TFIIIA reveals different tightly binding sites for 5S RNA and 5S DNA., Bogenhagen DF., Mol Cell Biol. September 1, 1993; 13 (9): 5149-58.

Selective recruitment of masked maternal mRNA from messenger ribonucleoprotein particles containing FRGY2 (mRNP4)., Tafuri SR., J Biol Chem. November 15, 1993; 268 (32): 24255-61.

A position-dependent transcription-activating domain in TFIIIA., Mao X., Mol Cell Biol. December 1, 1993; 13 (12): 7496-506.

Specific regulation of Xenopus chromosomal 5S rRNA gene transcription in vivo by histone H1., Bouvet P., Genes Dev. May 15, 1994; 8 (10): 1147-59.

Purification and characterization of human transcription factor IIIA., Moorefield B., J Biol Chem. August 19, 1994; 269 (33): 20857-65.

Overlapping transcription by RNA polymerases II and III of the Xenopus TFIIIA gene in somatic cells., Martinez E., J Biol Chem. October 14, 1994; 269 (41): 25692-8.

Characterization of the 5 S RNA binding activity of Xenopus zinc finger protein p43., Zang WQ., J Mol Biol. February 3, 1995; 245 (5): 549-58.

Differential binding of oocyte-type and somatic-type 5S rRNA to TFIIIA and ribosomal protein L5 in Xenopus oocytes: specialization for storage versus mobilization., Allison LA., Dev Biol. April 1, 1995; 168 (2): 284-95.

Analysis of the binding of Xenopus transcription factor IIIA to oocyte 5 S rRNA and to the 5 S rRNA gene., Rawlings SL., J Biol Chem. January 12, 1996; 271 (2): 868-77.

Nucleoskeleton and nucleo-cytoplasmic transport in oocytes and early development of Xenopus laevis., Rudt F., Int J Dev Biol. February 1, 1996; 40 (1): 273-8.

Molecular biology of vertebrate transcription factor IIIA: cloning and characterization of TFIIIA from channel catfish oocytes., Ogilvie MK., Gene. December 12, 1997; 203 (2): 103-12.

Nucleosome translational position, not histone acetylation, determines TFIIIA binding to nucleosomal Xenopus laevis 5S rRNA genes., Howe L., Mol Cell Biol. March 1, 1998; 18 (3): 1156-62.

Role of histone H1 as an architectural determinant of chromatin structure and as a specific repressor of transcription on Xenopus oocyte 5S rRNA genes., Sera T., Mol Cell Biol. July 1, 1998; 18 (7): 3668-80.

Differential nucleosome positioning on Xenopus oocyte and somatic 5 S RNA genes determines both TFIIIA and H1 binding: a mechanism for selective H1 repression., Panetta G., J Mol Biol. September 25, 1998; 282 (3): 683-97.

Inhibition of RNA polymerase III transcription by a ribosome-associated kinase activity., Westmark CJ., Nucleic Acids Res. October 15, 1998; 26 (20): 4758-64.

Tight correlation between inhibition of DNA repair in vitro and transcription factor IIIA binding in a 5S ribosomal RNA gene., Conconi A., EMBO J. March 1, 1999; 18 (5): 1387-96.

Regulation of DNA binding activity and nuclear transport of B-Myb in Xenopus oocytes., Humbert-Lan G., J Biol Chem. April 9, 1999; 274 (15): 10293-300.                

How do linker histones mediate differential gene expression?, Crane-Robinson C., Bioessays. May 1, 1999; 21 (5): 367-71.

Assembly of the nuclear transcription and processing machinery: Cajal bodies (coiled bodies) and transcriptosomes., Gall JG., Mol Biol Cell. December 1, 1999; 10 (12): 4385-402.

cDNA cloning, DNA binding, and evolution of mammalian transcription factor IIIA., Hanas JS., Gene. January 9, 2002; 282 (1-2): 43-52.

Phosphorylation of Xenopus transcription factor IIIA by an oocyte protein kinase CK2., Westmark CJ., Biochem J. March 1, 2002; 362 (Pt 2): 375-82.

DNA methylation at promoter regions regulates the timing of gene activation in Xenopus laevis embryos., Stancheva I., Dev Biol. March 1, 2002; 243 (1): 155-65.        

A homolog of FBP2/KSRP binds to localized mRNAs in Xenopus oocytes., Kroll TT., Development. December 1, 2002; 129 (24): 5609-19.        

The Xenopus B2 factor involved in TFIIIA gene regulation is closely related to Sp1 and interacts in a complex with USF., Penberthy WT., Gene. February 27, 2003; 305 (2): 205-15.

VgRBP71 stimulates cleavage at a polyadenylation signal in Vg1 mRNA, resulting in the removal of a cis-acting element that represses translation., Kolev NG., Mol Cell. March 1, 2003; 11 (3): 745-55.              

Binding of zinc finger protein transcription factor IIIA to its cognate DNA sequence with single UV photoproducts at specific sites and its effect on DNA repair., Kwon Y., J Biol Chem. November 14, 2003; 278 (46): 45451-9.

Restricted specificity of Xenopus TFIIIA for transcription of somatic 5S rRNA genes., Ghose R., Mol Cell Biol. March 1, 2004; 24 (6): 2467-77.

Zn-, Cd-, and Pb-transcription factor IIIA: properties, DNA binding, and comparison with TFIIIA-finger 3 metal complexes., Huang M., J Inorg Biochem. May 1, 2004; 98 (5): 775-85.

Small ubiquitin-like modifier (SUMO)-mediated repression of the Xenopus Oocyte 5 S rRNA genes., Malik MQ., J Biol Chem. December 19, 2014; 289 (51): 35468-81.                

In vitro chromatin templates to study nucleotide excision repair., Liu X., DNA Repair (Amst). December 1, 2015; 36 68-76.

Differential nuclear import sets the timing of protein access to the embryonic genome., Nguyen T., Nat Commun. October 6, 2022; 13 (1): 5887.                                  

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