Human cell growth regulator Ly‐1 antibody reactive homologue accelerates processing of preribosomal RNA

Ribosome biogenesis is an essential process for cell growth and proliferation and is enhanced in cancer and embryonic stem cells. Mouse Ly‐1 antibody reactive clone product (Lyar) is expressed at very high levels in many tumor, leukemia or embryonic stem cells; is a novel nucleolar protein with zinc...

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Veröffentlicht in:Genes to cells : devoted to molecular & cellular mechanisms 2014-04, Vol.19 (4), p.273-286
Hauptverfasser: Miyazawa, Naoki, Yoshikawa, Harunori, Magae, Satomi, Ishikawa, Hideaki, Izumikawa, Keiichi, Terukina, Goro, Suzuki, Ai, Nakamura‐Fujiyama, Sally, Miura, Yutaka, Hayano, Toshiya, Komatsu, Wataru, Isobe, Toshiaki, Takahashi, Nobuhiro
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container_end_page 286
container_issue 4
container_start_page 273
container_title Genes to cells : devoted to molecular & cellular mechanisms
container_volume 19
creator Miyazawa, Naoki
Yoshikawa, Harunori
Magae, Satomi
Ishikawa, Hideaki
Izumikawa, Keiichi
Terukina, Goro
Suzuki, Ai
Nakamura‐Fujiyama, Sally
Miura, Yutaka
Hayano, Toshiya
Komatsu, Wataru
Isobe, Toshiaki
Takahashi, Nobuhiro
description Ribosome biogenesis is an essential process for cell growth and proliferation and is enhanced in cancer and embryonic stem cells. Mouse Ly‐1 antibody reactive clone product (Lyar) is expressed at very high levels in many tumor, leukemia or embryonic stem cells; is a novel nucleolar protein with zinc‐finger DNA‐binding motifs and is involved in cell growth regulation. However, cellular function of Lyar remains unexplored. Here, we show that human homologue of Lyar (LYAR) accelerates ribosome biogenesis at the level of processing of preribosomal RNA (pre‐rRNA). We show that LYAR is excluded from the nucleolus after actinomycin D treatment and is present in preribosomal fraction of the nuclear extract as well as in the fractions with 40S, 60S and 90S sedimentation coefficients. LYAR is required for processing of 47S/45S, 32S, 30S and 21S pre‐rRNAs. In addition, we show that over‐expression of LYAR increases cell proliferation without affecting the expression of c‐Myc or p53. Combined, these results suggest that some rapidly growing cells enhance ribosome biogenesis by increasing the expression of LYAR.
doi_str_mv 10.1111/gtc.12129
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Mouse Ly‐1 antibody reactive clone product (Lyar) is expressed at very high levels in many tumor, leukemia or embryonic stem cells; is a novel nucleolar protein with zinc‐finger DNA‐binding motifs and is involved in cell growth regulation. However, cellular function of Lyar remains unexplored. Here, we show that human homologue of Lyar (LYAR) accelerates ribosome biogenesis at the level of processing of preribosomal RNA (pre‐rRNA). We show that LYAR is excluded from the nucleolus after actinomycin D treatment and is present in preribosomal fraction of the nuclear extract as well as in the fractions with 40S, 60S and 90S sedimentation coefficients. LYAR is required for processing of 47S/45S, 32S, 30S and 21S pre‐rRNAs. In addition, we show that over‐expression of LYAR increases cell proliferation without affecting the expression of c‐Myc or p53. 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subjects Animals
Biosynthesis
Cell growth
Cell Proliferation
Dactinomycin - pharmacology
DNA-Binding Proteins - genetics
DNA-Binding Proteins - metabolism
HEK293 Cells
HeLa Cells
Humans
Mice
Nuclear Proteins - genetics
Nuclear Proteins - metabolism
Nucleic Acid Synthesis Inhibitors - pharmacology
RNA Precursors - metabolism
RNA Processing, Post-Transcriptional
RNA, Ribosomal - metabolism
Stem cells
Structural Homology, Protein
title Human cell growth regulator Ly‐1 antibody reactive homologue accelerates processing of preribosomal RNA
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