B. Sollner-Webb

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In Trypanosoma brucei RNA Editing, Band II Enables Recognition Specifically at Each Step of the U Insertion Cycle

Julie A. Law, S. O’Hearn, Catherine E. Huang, 2005, Molecular and Cellular Biology.

Trypanosoma brucei RNA Editing: Coupled Cycles of U Deletion Reveal Processive Activity of the Editing Complex

J. Cruz-Reyes, B. Sollner-Webb, Vadim S Alatortsev, 2008, Molecular and Cellular Biology.

T. brucei RNA editing: action of the U-insertional TUTase within a U-deletion cycle.

Julie A Law, Julie A. Law, J. Cruz-Reyes, 2006, RNA.

Distinct Functions of Two RNA Ligases in Active Trypanosoma brucei RNA Editing Complexes

J. Cruz-Reyes, Catherine E. Huang, Barbara Sollner-Webb, 2002, Molecular and Cellular Biology.

RNA Editing in Trypanosomes

J. Cruz-Reyes, Catherine E. Huang, B. Sollner-Webb, 2001 .

Band V Gene Essential Band IV Gene and Identifying the RNA Editing Complex : Cloning the brucei Trypanosoma The Two RNA Ligases of the

K. Piller, L. Rusche, E. Wirtz, 2001 .

Trypanosome RNA Editing: Simple Guide RNA Features Enhance U Deletion 100-Fold

L. Rusche, J. Cruz-Reyes, B. Sollner-Webb, 2001, Molecular and Cellular Biology.

Ribonuclease activities of trypanosome RNA editing complex directed to cleave specifically at a chosen site.

L. Rusche, J. Cruz-Reyes, B. Sollner-Webb, 2001, Methods in enzymology.

Trypanosoma brucei U insertion and U deletion activities co-purify with an enzymatic editing complex but are differentially optimized.

L. Rusche, J. Cruz-Reyes, B. Sollner-Webb, 1998, Nucleic acids research.

T. brucei RNA editing: adenosine nucleotides inversely affect U-deletion and U-insertion reactions at mRNA cleavage.

K. Piller, L. Rusche, J. Cruz-Reyes, 1998, Molecular cell.

Trypanosome RNA Editin--Resolved

B. Sollner-Webb, B. Sollner‐Webb, 1996, Science.

Editing domains of Trypanosoma brucei mitochondrial RNAs identified by secondary structure

S. Hajduk, K. Piller, L. Rusche, 1995, Molecular and cellular biology.

Trypanosoma brucei mitochondrial guide RNA-mRNA chimera-forming activity cofractionates with an editing-domain-specific endonuclease and RNA ligase and is mimicked by heterologous nuclease and RNA ligase

K. Piller, L. Rusche, B. Sollner-Webb, 1995, Molecular and cellular biology.

Guides to experiments

B. Sollner-Webb, 1992, Nature.

Nucleotide sequence determining the first cleavage site in the processing of mouse precursor rRNA.

B. Sollner-Webb, N. Craig, S. Kass, 1987, Proceedings of the National Academy of Sciences of the United States of America.

Polymerase III transcription factor B activity is reduced in extracts of growth-restricted cells

J. Tower, B. Sollner-Webb, 1988 .

Polymerase III transcription factor B activity is reduced in extracts of growth-restricted cells

J. Tower, B. Sollner-Webb, 1988, Molecular and cellular biology.

A U3 small nuclear ribonucleoprotein-requiring processing event in the 5' external transcribed spacer of Xenopus precursor rRNA

E. Mougey, B. Sollner-Webb, L. Pape, 1993, Molecular and cellular biology.

5'ETS rRNA processing facilitated by four small RNAs: U14, E3, U17, and U3.

E. Maxwell, B. Sollner-Webb, G. L. Eliceiri, 1996, RNA.

In Trypanosoma brucei RNA Editing, Band II Enables Recognition Specifically at Each Step of the U Insertion Cycle

Julie A. Law, S. O’Hearn, Catherine E. Huang, 2005, Molecular and Cellular Biology.

Trypanosoma brucei RNA editing protein TbMP42 (band VI) is crucial for the endonucleolytic cleavages but not the subsequent steps of U-deletion and U-insertion.

Julie A. Law, S. O’Hearn, B. Sollner-Webb, 2008, RNA.

In Trypanosoma brucei RNA Editing, TbMP18 (Band VII) Is Critical for Editosome Integrity and for both Insertional and Deletional Cleavages

Julie A. Law, S. O’Hearn, B. Sollner-Webb, 2006, Molecular and Cellular Biology.

Trypanosome U-deletional RNA editing involves guide RNA-directed endonuclease cleavage, terminal U exonuclease, and RNA ligase activities.

J. Cruz-Reyes, B. Sollner-Webb, B. Sollner‐Webb, 1996, Proceedings of the National Academy of Sciences of the United States of America.

Direct sizing of RNA fragments using RNase-generated standards.

L. Rusche, J. Cruz-Reyes, B. Sollner-Webb, 2001, Methods in enzymology.

The Xenopus ribosomal DNA 60- and 81-base-pair repeats are position-dependent enhancers that function at the establishment of the preinitiation complex: analysis in vivo and in an enhancer-responsive in vitro system

J. Windle, E. Mougey, B. Sollner-Webb, 1989, Molecular and cellular biology.

Prediction of Gene Activity in Early B Cell Development Based on an Integrative Multi-Omics Analysis

Christopher J. Mitchell, A. Pandey, Min-Sik Kim, 2014, Journal of proteomics & bioinformatics.

Analysis of nucleolar transcription and processing domains and pre-rRNA movements by in situ hybridization

Michael. Delannoy, B. Sollner-Webb, I. Lazdins, 1997, Chromosoma.

Surprising S1-Resistant Trimolecular Hybrids: Potential

D. Cleveland, B. Sollner-Webb, M. Lopata, 2003 .

Stimulation of the mouse rRNA gene promoter by a distal spacer promoter

M. Paalman, B. Sollner-Webb, S. Henderson, 1995, Molecular and cellular biology.

DNA FOLDING AND HISTONE ORGANIZATION IN CHROMATIN

P. Williamson, G. Felsenfeld, R. Camerini-Otero, 1978 .

Specific sites of interaction between histones and DNA in chromatin.

R. Axel, G. Felsenfeld, B. Sollner-Webb, 1974, Proceedings of the National Academy of Sciences of the United States of America.

Stable integrative transformation of Trypanosoma brucei that occurs exclusively by homologous recombination.

B. Sollner-Webb, J. Eid, Josiane E. Eid, 1991, Proceedings of the National Academy of Sciences of the United States of America.

ST-1, a 39-kilodalton protein in Trypanosoma brucei, exhibits a dual affinity for the duplex form of the 29-base-pair subtelomeric repeat and its C-rich strand

B. Sollner-Webb, J. Eid, B. Sollner‐Webb, 1995, Molecular and cellular biology.

ST-2, a Telomere and Subtelomere Duplex and G-strand Binding Protein Activity in Trypanosoma brucei*

J. E. Eid, B. Sollner-Webb, 1997, The Journal of Biological Chemistry.

Transcription of mouse rDNA is regulated by an activated subform of RNA polymerase I

J. Tower, B. Sollner-Webb, B. Sollner‐Webb, 1987, Cell.

Factor C*, the specific initiation component of the mouse RNA polymerase I holoenzyme, is inactivated early in the transcription process

R. Brun, B. Sollner-Webb, K. Ryan, 1994, Molecular and cellular biology.

A transcriptional terminator is a novel element of the promoter of the mouse ribosomal RNA gene

B. Sollner-Webb, S. Henderson, B. Sollner‐Webb, 1986, Cell.

The first pre-rRNA-processing event occurs in a large complex: analysis by gel retardation, sedimentation, and UV cross-linking

B. Sollner-Webb, S. Kass, B. Sollner‐Webb, 1990, Molecular and cellular biology.

Primary processing of mammalian rRNA involves two adjacent cleavages and is not species specific

B. Sollner-Webb, N. Craig, S. Kass, 1987, Molecular and cellular biology.

Enhancers for RNA polymerase I in mouse ribosomal DNA

C. Pikaard, M. Paalman, R. Reeder, 1990, Molecular and cellular biology.

Half helical turn spacing changes convert a frog into a mouse rDNA promoter: a distant upstream domain determines the helix face of the initiation site.

J. Windle, B. Sollner-Webb, L. Pape, 1990, Genes & development.

Mouse and frog violate the paradigm of species-specific transcription of ribosomal RNA genes.

V. Culotta, B. Sollner-Webb, J. Wilkinson, 1987, Proceedings of the National Academy of Sciences of the United States of America.

A complex control region of the mouse rRNA gene directs accurate initiation by RNA polymerase I

J. Tower, K. Miller, B. Sollner-Webb, 1985, Molecular and cellular biology.

Sequence organization and RNA structural motifs directing the mouse primary rRNA-processing event

B. Sollner-Webb, N. Craig, S. Kass, 1991, Molecular and cellular biology.

Transcription of mouse rRNA genes by RNA polymerase I: In vitro and in vivo initiation and processing sites

K. Miller, B. Sollner-Webb, B. Sollner‐Webb, 1981, Cell.

Surprising S1-resistant trimolecular hybrids: potential complication in interpretation of S1 mapping analyses

D. Cleveland, B. Sollner-Webb, M. Lopata, 1985, Molecular and cellular biology.

Upstream domains of the Xenopus laevis rDNA promoter are revealed in microinjected oocytes

J. Windle, B. Sollner-Webb, B. Sollner‐Webb, 1986, Molecular and cellular biology.

Nested control regions promote Xenopus ribosomal RNA synthesis by RNA polymerase I

R. Reeder, B. Sollner-Webb, J. Roan, 1983, Cell.

Pancreatic DNAase cleavage sites in nuclei

G. Felsenfeld, B. Sollner-Webb, B. Sollner‐Webb, 1977, Cell.

Trypanosoma brucei RNA Editing Complex: Band II Is Structurally Critical and Maintains Band V Ligase, Which Is Nonessential

S. O’Hearn, Catherine E. Huang, B. Sollner-Webb, 2003 .

An RNA polymerase I promoter located in the CHO and mouse ribosomal DNA spacers: functional analysis and factor and sequence requirements

J. Tower, B. Sollner-Webb, K. Dougherty, 1989, Molecular and cellular biology.

Two distant and precisely positioned domains promote transcription of Xenopus laevis rRNA genes: analysis with linker-scanning mutants

J. Windle, B. Sollner-Webb, 1986, Molecular and cellular biology.

The Specific Template Activity of Chromatin

R. Axel, H. Cedar, G. Felsenfeld, 2008 .

Transcription of Ribosomal RNA Genes in Mouse and Frog

R. Wides, K. Miller, R. Reeder, 1984 .

Eucaryotic transcription complexes are specifically associated in large sedimentable structures: rapid isolation of polymerase I, II, and III transcription factors

R. Wides, V. Culotta, B. Sollner-Webb, 1985, Molecular and cellular biology.

TheFirst Pre-rRNA-Processing EventOccursina LargeComplex: Analysis byGelRetardation, Sedimentation, andUV Cross-Linking

B. Sollner-Webb, 1990 .

Transcription of cloned eukaryotic ribosomal RNA genes.

J. Tower, B. Sollner-Webb, Barbara Sollner-Webb, 1986, Annual review of biochemistry.

The absence of a human-specific ribosomal DNA transcription factor leads to nucleolar dominance in mouse greater than human hybrid cells

N. Arnheim, R. Miesfeld, B. Sollner-Webb, 1984, Molecular and cellular biology.

Nucleosome structure, DNA folding, and gene activity.

P. Williamson, G. Felsenfeld, R. Camerini-Otero, 1978, Cold Spring Harbor symposia on quantitative biology.

High level transient expression of a chloramphenicol acetyl transferase gene by DEAE-dextran mediated DNA transfection coupled with a dimethyl sulfoxide or glycerol shock treatment.

B Sollner-Webb, D. Cleveland, D W Cleveland, 1984, Nucleic acids research.

Sites of topoisomerase I action on X. laevis ribosomal chromatin: Transcriptionally active rDNA has an ∼200 bp repeating structure

V. Culotta, B. Sollner-Webb, B. Sollner‐Webb, 1988, Cell.

A rapidly rearranging retrotransposon within the miniexon gene locus of Crithidia fasciculata.

D. Schwartz, J. Boeke, C. Smith, 1990, Molecular and cellular biology.

A comparison of the digestion of nuclei and chromatin by staphylococcal nuclease.

G. Felsenfeld, B. Sollner-Webb, B. Sollner‐Webb, 1975, Biochemistry.

Specificity of RNA maturation pathways: RNAs transcribed by RNA polymerase III are not substrates for splicing or polyadenylation

D. Cleveland, S. Sisodia, B. Sollner-Webb, 1987, Molecular and cellular biology.

Specificity ofRNA Maturation Pathways: RNAsTranscribed by RNA Polymerase IIIAreNotSubstrates forSplicing or Polyadenylation

B. Sollner-Webb, B. Sollner‐Webb, 1987 .

Mapping of transcription initiation and termination signals on Xenopus laevis ribosomal DNA.

R. Reeder, B. Sollner-Webb, A. Bakken, 1982, Proceedings of the National Academy of Sciences of the United States of America.

The nucleotide sequence of the initiation and termination sites for ribosomal rna transcription in x. laevis

R. Reeder, B. Sollner-Webb, B. Sollner‐Webb, 1979, Cell.

The organization of histones and DNA in chromatin: Evidence for an arginine-rich histone kernel

G. Felsenfeld, R. Camerini-Otero, B. Sollner-Webb, 1976, Cell.

PROTEIN INTERACTION WITH DNA IN CHROMATIN

G. Felsenfeld, B. Sollner-Webb, B. Sollner‐Webb, 1975 .

Novel intron-encoded small nucleolar RNAs

B. Sollner-Webb, B. Sollner‐Webb, 1993, Cell.

The U3 small nucleolar ribonucleoprotein functions in the first step of preribosomal RNA processing

J. Steitz, B. Sollner-Webb, S. Kass, 1990, Cell.

RNA editing involves indiscriminate U changes throughout precisely defined editing domains

B. Sollner-Webb, C. Decker, B. Sollner‐Webb, 1990, Cell.

The promoter-proximal rDNA terminator augments initiation by preventing disruption of the stable transcription complex caused by polymerase read-in.

B. Sollner-Webb, S. Henderson, K. Ryan, 1989, Genes & development.

Trypanosoma brucei RNA Editing Complex

S. O’Hearn, Catherine E. Huang, B. Sollner-Webb, 2003, Molecular and Cellular Biology.

The Two RNA Ligases of the Trypanosoma brucei RNA Editing Complex: Cloning the Essential Band IV Gene and Identifying the Band V Gene

K. Piller, L. Rusche, E. Wirtz, 2001, Molecular and Cellular Biology.

The mouse ribosomal DNA promoter has more stringent requirements in vivo than in vitro

B. Sollner-Webb, S. Henderson, B. Sollner‐Webb, 1990, Molecular and cellular biology.

Surprises in polymerase III transcription

B. Sollner-Webb, B. Sollner‐Webb, 1988, Cell.

Ribosomal genes and their proteins from Xenopus.

R. Hipskind, R. Reeder, B. Sollner-Webb, 1978, Cold Spring Harbor symposia on quantitative biology.

Sites of transcription initiation in vivo on Xenopus laevis ribosomal DNA.

R. Reeder, B. Sollner-Webb, H. Wahn, 1977, Proceedings of the National Academy of Sciences of the United States of America.

Transcription of Xenopus ribosomal RNA genes by RNA polymerase I in vitro.

B. Sollner-Webb, J. Wilkinson, 1982, The Journal of biological chemistry.

News from the nucleolus: rRNA gene expression.

E. Mougey, B. Sollner-Webb, B. Sollner‐Webb, 1991, Trends in biochemical sciences.

The terminal balls characteristic of eukaryotic rRNA transcription units in chromatin spreads are rRNA processing complexes.

M. O'Reilly, Y. Osheim, O. Miller, 1993, Genes & development.

Factors and nucleotide sequences that direct ribosomal DNA transcription and their relationship to the stable transcription complex

J. Tower, V. Culotta, B. Sollner-Webb, 1986, Molecular and cellular biology.

Homologous recombination in the tandem calmodulin genes of Trypanosoma brucei yields multiple products: compensation for deleterious deletions by gene amplification.

B. Sollner-Webb, J. Eid, B. Sollner‐Webb, 1991, Genes & development.

Accurate transcription of cloned Xenopus rRNA genes by RNA polymerase I: demonstration by S1 nuclease mapping.

S. McKnight, B. Sollner-Webb, B. Sollner‐Webb, 1982, Nucleic acids research.

Virtually the Entire Xenopus laevis rDNA Multikilobase Intergenic Spacer Serves to Stimulate Polymerase I Transcription*

E. Mougey, B. Sollner-Webb, L. Pape, 1996, The Journal of Biological Chemistry.

Metazoan rDNA enhancer acts by making more genes transcriptionally active

B Sollner-Webb, M. O'Reilly, J. Windle, 1996, The Journal of cell biology.

Enhancers forRNA Polymerase IinMouseRibosomal DNA

B. Sollner-Webb, K. Ryan, B. Sollner‐Webb, 1990 .

DNAase I, DNAase II and staphylococcal nuclease cut at different, yet symmetrically located, sites in the nucleosome core

G. Felsenfeld, B. Sollner-Webb, W. Melchior, 1978, Cell.

A stable transcription complex directs mouse ribosomal RNA synthesis by RNA polymerase I.

B. Sollner-Webb, V. Cizewski, B. Sollner‐Webb, 1983, Nucleic acids research.

Chromatin structure as probed by nucleases and proteases: Evidence for the central role of hitones H3 and H4

G. Felsenfeld, R. Camerini-Otero, B. Sollner-Webb, 1976, Cell.

TheXenopusRibosomal DNA 60-and81-Base-Pair Repeats Are Position-Dependent Enhancers ThatFunction attheEstablishment ofthePreinitiation Complex: Analysis InVivoandinan Enhancer-Responsive

B. Sollner-Webb, B. Sollner‐Webb, 1989 .

A combination of RNase H and S1 nuclease circumvents an artefact inherent to conventional S1 analysis of RNA splicing.

D. Cleveland, S. Sisodia, B. Sollner-Webb, 1987, Nucleic acids research.

RNA polymerase specificity of mRNA production and enhancer action.

D. Cleveland, B. Sollner-Webb, M. Lopata, 1986, Proceedings of the National Academy of Sciences of the United States of America.

Dinucleotide primers facilitate convenient identification of the mouse ribosomal DNA transcription initiation site. A general method for analysis of transcription by RNA polymerases I and III.

K. Miller, B. Sollner-Webb, J. A. Wilkinson, 1983, The Journal of biological chemistry.

Expression of mouse and frog rRNA genes: transcription and processing

M. Paalman, C. Martin, E. Mougey, 2004, Molecular and Cellular Biochemistry.

Guide RNA-mRNA chimeras, which are potential RNA editing intermediates, are formed by endonuclease and RNA ligase in a trypanosome mitochondrial extract

L N Rusché, K J Piller, B Sollner-Webb, 1995, Molecular and cellular biology.

Assembly and Function of the RNA Editing Complex in Trypanosoma brucei Requires Band III Protein

S. O’Hearn, Catherine E. Huang, Sean F. O'Hearn, 2002, Molecular and Cellular Biology.

Purification of a functional enzymatic editing complex from Trypanosoma brucei mitochondria

K. Piller, L. Rusche, J. Cruz-Reyes, 1997, The EMBO journal.

Resolution of the RNA editing gRNA-directed endonuclease from two other endonucleases of Trypanosoma brucei mitochondria.

L N Rusché, K J Piller, B Sollner-Webb, 1997, RNA.

Specific cleavage of pre-edited mRNAs in trypanosome mitochondrial extracts

S. Hajduk, M. Harris, B. Sollner-Webb, 1992, Molecular and cellular biology.

Unexpected electrophoretic migration of RNA with different 3' termini causes a RNA sizing ambiguity that can be resolved using nuclease P1-generated sequencing ladders.

L N Rusché, B Sollner-Webb, J Cruz-Reyes, 1998, Biochemistry.