Literature DB >> 8293976

Molecular genetics of cryptopleurine resistance in Saccharomyces cerevisiae: expression of a ribosomal protein gene family.

A G Paulovich1, J R Thompson, J C Larkin, Z Li, J L Woolford.   

Abstract

The Saccharomyces cerevisiae CRY1 gene encodes the 40S ribosomal subunit protein rp59 and confers sensitivity to the protein synthesis inhibitor cryptopleurine. A yeast strain containing the cry1-delta 1::URA3 null allele is viable, cryptopleurine sensitive (CryS), and expresses rp59 mRNA, suggesting that there is a second functional CRY gene. The CRY2 gene has been isolated from a yeast genomic library cloned in bacteriophage lambda, using a CRY1 DNA probe. The DNA sequence of the CRY2 gene contains an open reading frame encoding ribosomal protein 59 that differs at five residues from rp59 encoded by the CRY1 gene. The CRY2 gene was mapped to the left arm of chromosome X, centromere-proximal to cdc6 and immediately adjacent to ribosomal protein genes RPS24A and RPL46. Ribosomal protein 59 is an essential protein; upon sporulation of a diploid doubly heterozygous for cry1-delta 2::TRP1 cry2-delta 1::LEU2 null alleles, no spore clones containing both null alleles were recovered. Several results indicate that CRY2 is expressed, but at lower levels than CRY1: (1) Introduction of CRY2 on high copy plasmids into CryR yeast of genotype cry1 CRY2 confers a CryS phenotype. Transformation of these CryR yeast with CRY2 on a low copy CEN plasmid does not confer a CryS phenotype. (2) Haploids containing the cry1-delta 2::TRP1 null allele have a deficit of 40S ribosomal subunits, but cry2-delta 1::LEU2 strains have wild-type amounts of 40S ribosomal subunits. (3) CRY2 mRNA is present at lower levels than CRY1 mRNA. (4) Higher levels of beta-galactosidase are expressed from a CRY1-lacZ gene fusion than from a CRY2-lacZ gene fusion. Mutations that alter or eliminate the last amino acid of rp59 encoded by either CRY1 or CRY2 result in resistance to cryptopleurine. Because CRY2 (and cry2) is expressed at lower levels than CRY1 (and cry1), the CryR phenotype of cry2 mutants is only expressed in strains containing a cry1-delta null allele.

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Year:  1993        PMID: 8293976      PMCID: PMC1205715     

Source DB:  PubMed          Journal:  Genetics        ISSN: 0016-6731            Impact factor:   4.562


  32 in total

1.  Expression of cryptopleurine resistance in Saccharomyces cerevisiae.

Authors:  J H Meade; M I Riley; T R Manney
Journal:  J Bacteriol       Date:  1977-03       Impact factor: 3.490

2.  Transformation in yeast: development of a hybrid cloning vector and isolation of the CAN1 gene.

Authors:  J R Broach; J N Strathern; J B Hicks
Journal:  Gene       Date:  1979-12       Impact factor: 3.688

3.  The isolation of structural genes from libraries of eucaryotic DNA.

Authors:  T Maniatis; R C Hardison; E Lacy; J Lauer; C O'Connell; D Quon; G K Sim; A Efstratiadis
Journal:  Cell       Date:  1978-10       Impact factor: 41.582

4.  Quantitation of the specific interaction of [14a-3H]cryptopleurine with 80S and 40S ribosomal species from the yeast Saccharomyces cerevisiae.

Authors:  H Dölz; D Vázquez; A Jiménez
Journal:  Biochemistry       Date:  1982-06-22       Impact factor: 3.162

5.  Modification of ribosomes in cryptopleurine-resistant mutants of yeast.

Authors:  L Skogerson; C McLaughlin; E Wakatama
Journal:  J Bacteriol       Date:  1973-11       Impact factor: 3.490

6.  Cryptopleurine--an inhibitor of translocation.

Authors:  K Bucher; L Skogerson
Journal:  Biochemistry       Date:  1976-11-02       Impact factor: 3.162

7.  The effect of temperature-sensitive RNA mutants on the transcription products from cloned ribosomal protein genes of yeast.

Authors:  M Rosbash; P K Harris; J L Woolford; J L Teem
Journal:  Cell       Date:  1981-06       Impact factor: 41.582

8.  Ribosomal protein genes rp 39(10 - 78), rp 39(11 - 40), rp 51, and rp 52 are not contiguous to other ribosomal protein genes in the Saccharomyces cerevisiae genome.

Authors:  J L Woolford; M Rosbash
Journal:  Nucleic Acids Res       Date:  1981-10-10       Impact factor: 16.971

9.  Two differentially regulated mRNAs with different 5' ends encode secreted with intracellular forms of yeast invertase.

Authors:  M Carlson; D Botstein
Journal:  Cell       Date:  1982-01       Impact factor: 41.582

10.  Use of a screen for synthetic lethal and multicopy suppressee mutants to identify two new genes involved in morphogenesis in Saccharomyces cerevisiae.

Authors:  A Bender; J R Pringle
Journal:  Mol Cell Biol       Date:  1991-03       Impact factor: 4.272

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  13 in total

1.  Yeast Krr1p physically and functionally interacts with a novel essential Kri1p, and both proteins are required for 40S ribosome biogenesis in the nucleolus.

Authors:  T Sasaki; A Toh-E; Y Kikuchi
Journal:  Mol Cell Biol       Date:  2000-11       Impact factor: 4.272

2.  The C-terminal region of eukaryotic translation initiation factor 3a (eIF3a) promotes mRNA recruitment, scanning, and, together with eIF3j and the eIF3b RNA recognition motif, selection of AUG start codons.

Authors:  Wen-Ling Chiu; Susan Wagner; Anna Herrmannová; Laxminarayana Burela; Fan Zhang; Adesh K Saini; Leos Valásek; Alan G Hinnebusch
Journal:  Mol Cell Biol       Date:  2010-06-28       Impact factor: 4.272

3.  Ribosomal protein S14 of Saccharomyces cerevisiae regulates its expression by binding to RPS14B pre-mRNA and to 18S rRNA.

Authors:  S W Fewell; J L Woolford
Journal:  Mol Cell Biol       Date:  1999-01       Impact factor: 4.272

4.  The target of rapamycin signaling pathway regulates mRNA turnover in the yeast Saccharomyces cerevisiae.

Authors:  A R Albig; C J Decker
Journal:  Mol Biol Cell       Date:  2001-11       Impact factor: 4.138

5.  Novel G-protein complex whose requirement is linked to the translational status of the cell.

Authors:  Anne Carr-Schmid; Christine Pfund; Elizabeth A Craig; Terri Goss Kinzy
Journal:  Mol Cell Biol       Date:  2002-04       Impact factor: 4.272

6.  An RNA structure involved in feedback regulation of splicing and of translation is critical for biological fitness.

Authors:  B Li; J Vilardell; J R Warner
Journal:  Proc Natl Acad Sci U S A       Date:  1996-02-20       Impact factor: 11.205

7.  The CRY1 gene in Chlamydomonas reinhardtii: structure and use as a dominant selectable marker for nuclear transformation.

Authors:  J A Nelson; P B Savereide; P A Lefebvre
Journal:  Mol Cell Biol       Date:  1994-06       Impact factor: 4.272

8.  The small subunit processome is required for cell cycle progression at G1.

Authors:  Kara A Bernstein; Susan J Baserga
Journal:  Mol Biol Cell       Date:  2004-09-08       Impact factor: 4.138

9.  The duplicated Saccharomyces cerevisiae gene SSM1 encodes a eucaryotic homolog of the eubacterial and archaebacterial L1 ribosomal proteins.

Authors:  A Petitjean; N Bonneaud; F Lacroute
Journal:  Mol Cell Biol       Date:  1995-09       Impact factor: 4.272

10.  Feedback inhibition of the yeast ribosomal protein gene CRY2 is mediated by the nucleotide sequence and secondary structure of CRY2 pre-mRNA.

Authors:  Z Li; A G Paulovich; J L Woolford
Journal:  Mol Cell Biol       Date:  1995-11       Impact factor: 4.272

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