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Metabolism and regulation of canonical histone mRNAs: life without a poly(A) tail

Nature reviews. Genetics, 2008-11, Vol.9 (11), p.843-854

2008

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Coordinating cell cycle-regulated histone gene expression through assembly and function of the Histone Locus Body

RNA biology, 2017-06, Vol.14 (6), p.726-738

2017

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CDK-Regulated Phase Separation Seeded by Histone Genes Ensures Precise Growth and Function of Histone Locus Bodies

Developmental cell, 2020-08, Vol.54 (3), p.379-394.e6

2020

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Degradation of histone mRNA requires oligouridylation followed by decapping and simultaneous degradation of the mRNA both 5' to 3' and 3' to 5'

Genes & development, 2008-01, Vol.22 (1), p.50-65

2008

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Structure of an active human histone pre-mRNA 3'-end processing machinery

Science (American Association for the Advancement of Science), 2020-02, Vol.367 (6478), p.700-703

2020

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Dual RNA 3’-end processing of H2A.X messenger RNA maintains DNA damage repair throughout the cell cycle

Nature communications, 2021-01, Vol.12 (1), p.359-359, Article 359

2021

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Structure of Histone mRNA Stem-Loop, Human Stem-Loop Binding Protein, and 3′hExo Ternary Complex

Science (American Association for the Advancement of Science), 2013-01, Vol.339 (6117), p.318-321

2013

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Tissue-Dependent Expression and Translation of Circular RNAs with Recombinant AAV Vectors In Vivo

Molecular therapy. Nucleic acids, 2018-12, Vol.13, p.89-98

2018

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Formation of the 3′ end of histone mRNA: Getting closer to the end

Gene, 2007-07, Vol.396 (2), p.373-390

2007

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Concentrating pre-mRNA processing factors in the histone locus body facilitates efficient histone mRNA biogenesis

The Journal of cell biology, 2016-06, Vol.213 (5), p.557-570

2016

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Regulated degradation of replication-dependent histone mRNAs requires both ATR and Upf1

Nature structural & molecular biology, 2005-09, Vol.12 (9), p.794-800

2005

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A subset of replication-dependent histone mRNAs are expressed as polyadenylated RNAs in terminally differentiated tissues

Nucleic acids research, 2016-11, Vol.44 (19), p.9190

2016

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Rare Codons Regulate KRas Oncogenesis

Current biology, 2013-01, Vol.23 (1), p.70-75

2013

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Protein composition of catalytically active U7-dependent processing complexes assembled on histone pre-mRNA containing biotin and a photo-cleavable linker

Nucleic acids research, 2018-05, Vol.46 (9), p.4752-4770

2018

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Deep Sequencing Shows Multiple Oligouridylations Are Required for 3′ to 5′ Degradation of Histone mRNAs on Polyribosomes

Molecular cell, 2014-03, Vol.53 (6), p.1020-1030

2014

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Metazoan replication-dependent histone mRNAs: a distinct set of RNA polymerase II transcripts

Current opinion in cell biology, 2005-06, Vol.17 (3), p.274-280

Marzluff, William F

2005

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A Core Complex of CPSF73, CPSF100, and Symplekin May Form Two Different Cleavage Factors for Processing of Poly(A) and Histone mRNAs

Molecular cell, 2009-05, Vol.34 (3), p.322-332

2009

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Engineering highly efficient backsplicing and translation of synthetic circRNAs

Molecular therapy. Nucleic acids, 2021-03, Vol.23, p.821-834

2021

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FLASH, a Proapoptotic Protein Involved in Activation of Caspase-8, Is Essential for 3′ End Processing of Histone Pre-mRNAs

Molecular cell, 2009-10, Vol.36 (2), p.267-278

2009

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A standardized nomenclature for mammalian histone genes

Epigenetics & chromatin, 2022-10, Vol.15 (1), p.34-34, Article 34

2022

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A Sequence in the Drosophila H3-H4 Promoter Triggers Histone Locus Body Assembly and Biosynthesis of Replication-Coupled Histone mRNAs

Developmental cell, 2013-03, Vol.24 (6), p.623-634

2013

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Birth and Death of Histone mRNAs

Trends in genetics, 2017-10, Vol.33 (10), p.745-759

2017

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The Polyadenylation Factor CPSF-73 Is Involved in Histone-Pre-mRNA Processing

Cell, 2005-10, Vol.123 (1), p.37-48

2005

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The N-terminal domains of FLASH and Lsm11 form a 2:1 heterotrimer for histone pre-mRNA 3'-end processing

PloS one, 2017-10, Vol.12 (10), p.e0186034-e0186034

2017

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A Complex Containing the CPSF73 Endonuclease and Other Polyadenylation Factors Associates with U7 snRNP and Is Recruited to Histone Pre-mRNA for 3′-End Processing

Molecular and Cellular Biology, 2013-01, Vol.33 (1), p.28-37

2013

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Metabolism and regulation of canonical histone mRNAs: life without a poly(A) tail

Coordinating cell cycle-regulated histone gene expression through assembly and function of the Histone Locus Body

CDK-Regulated Phase Separation Seeded by Histone Genes Ensures Precise Growth and Function of Histone Locus Bodies

Degradation of histone mRNA requires oligouridylation followed by decapping and simultaneous degradation of the mRNA both 5' to 3' and 3' to 5'

Structure of an active human histone pre-mRNA 3'-end processing machinery

Dual RNA 3’-end processing of H2A.X messenger RNA maintains DNA damage repair throughout the cell cycle

Structure of Histone mRNA Stem-Loop, Human Stem-Loop Binding Protein, and 3′hExo Ternary Complex

Tissue-Dependent Expression and Translation of Circular RNAs with Recombinant AAV Vectors In Vivo

Formation of the 3′ end of histone mRNA: Getting closer to the end

Concentrating pre-mRNA processing factors in the histone locus body facilitates efficient histone mRNA biogenesis

Regulated degradation of replication-dependent histone mRNAs requires both ATR and Upf1

A subset of replication-dependent histone mRNAs are expressed as polyadenylated RNAs in terminally differentiated tissues

Rare Codons Regulate KRas Oncogenesis

Protein composition of catalytically active U7-dependent processing complexes assembled on histone pre-mRNA containing biotin and a photo-cleavable linker

Deep Sequencing Shows Multiple Oligouridylations Are Required for 3′ to 5′ Degradation of Histone mRNAs on Polyribosomes

Metazoan replication-dependent histone mRNAs: a distinct set of RNA polymerase II transcripts

A Core Complex of CPSF73, CPSF100, and Symplekin May Form Two Different Cleavage Factors for Processing of Poly(A) and Histone mRNAs

Engineering highly efficient backsplicing and translation of synthetic circRNAs

FLASH, a Proapoptotic Protein Involved in Activation of Caspase-8, Is Essential for 3′ End Processing of Histone Pre-mRNAs

A standardized nomenclature for mammalian histone genes

A Sequence in the Drosophila H3-H4 Promoter Triggers Histone Locus Body Assembly and Biosynthesis of Replication-Coupled Histone mRNAs

Birth and Death of Histone mRNAs

The Polyadenylation Factor CPSF-73 Is Involved in Histone-Pre-mRNA Processing

The N-terminal domains of FLASH and Lsm11 form a 2:1 heterotrimer for histone pre-mRNA 3'-end processing

A Complex Containing the CPSF73 Endonuclease and Other Polyadenylation Factors Associates with U7 snRNP and Is Recruited to Histone Pre-mRNA for 3′-End Processing

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