Detail
Article
Online article
FT
Medvik - BMC
  • Something wrong with this record ?

A large number of nuclear genes in the human parasite blastocystis require mRNA polyadenylation to create functional termination codons

V. Klimeš, E. Gentekaki, AJ. Roger, M. Eliáš,

. 2014 ; 6 (8) : 1956-61.

Language English Country England, Great Britain

Document type Letter, Research Support, Non-U.S. Gov't

Termination codons in mRNA molecules are typically specified directly by the sequence of the corresponding gene. However, in mitochondria of a few eukaryotic groups, some mRNAs contain the termination codon UAA deriving one or both adenosines from transcript polyadenylation. Here, we show that a similar phenomenon occurs for a substantial number of nuclear genes in Blastocystis spp., divergent unicellular eukaryote gut parasites. Our analyses of published genomic data from Blastocystis sp. subtype 7 revealed that polyadenylation-mediated creation of termination codons occurs in approximately 15% of all nuclear genes. As this phenomenon has not been noticed before, the procedure previously employed to annotate the Blastocystis nuclear genome sequence failed to correctly define the structure of the 3'-ends of hundreds of genes. From sequence data we have obtained from the distantly related Blastocystis sp. subtype 1 strain, we show that this phenomenon is widespread within the Blastocystis genus. Polyadenylation in Blastocystis appears to be directed by a conserved GU-rich element located four nucleotides downstream of the polyadenylation site. Thus, the highly precise positioning of the polyadenylation in Blastocystis has allowed reduction of the 3'-untranslated regions to the point that, in many genes, only one or two nucleotides of the termination codon are left.

References provided by Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc15023265
003      
CZ-PrNML
005      
20150729122609.0
007      
ta
008      
150709s2014 enk f 000 0|eng||
009      
AR
024    7_
$a 10.1093/gbe/evu146 $2 doi
035    __
$a (PubMed)25015079
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a enk
100    1_
$a Klimeš, Vladimír $u Department of Biology and Ecology, Faculty of Science, University of Ostrava, Czech Republic.
245    12
$a A large number of nuclear genes in the human parasite blastocystis require mRNA polyadenylation to create functional termination codons / $c V. Klimeš, E. Gentekaki, AJ. Roger, M. Eliáš,
520    9_
$a Termination codons in mRNA molecules are typically specified directly by the sequence of the corresponding gene. However, in mitochondria of a few eukaryotic groups, some mRNAs contain the termination codon UAA deriving one or both adenosines from transcript polyadenylation. Here, we show that a similar phenomenon occurs for a substantial number of nuclear genes in Blastocystis spp., divergent unicellular eukaryote gut parasites. Our analyses of published genomic data from Blastocystis sp. subtype 7 revealed that polyadenylation-mediated creation of termination codons occurs in approximately 15% of all nuclear genes. As this phenomenon has not been noticed before, the procedure previously employed to annotate the Blastocystis nuclear genome sequence failed to correctly define the structure of the 3'-ends of hundreds of genes. From sequence data we have obtained from the distantly related Blastocystis sp. subtype 1 strain, we show that this phenomenon is widespread within the Blastocystis genus. Polyadenylation in Blastocystis appears to be directed by a conserved GU-rich element located four nucleotides downstream of the polyadenylation site. Thus, the highly precise positioning of the polyadenylation in Blastocystis has allowed reduction of the 3'-untranslated regions to the point that, in many genes, only one or two nucleotides of the termination codon are left.
650    _2
$a sekvence aminokyselin $7 D000595
650    _2
$a sekvence nukleotidů $7 D001483
650    _2
$a Blastocystis $x chemie $x genetika $7 D016844
650    _2
$a blastocystóza $x parazitologie $7 D016776
650    _2
$a terminační kodon $x chemie $x genetika $7 D018388
650    _2
$a lidé $7 D006801
650    _2
$a molekulární sekvence - údaje $7 D008969
650    12
$a polyadenylace $7 D026723
650    _2
$a protozoální proteiny $x chemie $x genetika $7 D015800
650    _2
$a messenger RNA $x chemie $x genetika $7 D012333
655    _2
$a dopisy $7 D016422
655    _2
$a práce podpořená grantem $7 D013485
700    1_
$a Gentekaki, Eleni $u Department of Biochemistry and Molecular Biology, Dalhousie University, Halifax, Nova Scotia, Canada.
700    1_
$a Roger, Andrew J $u Department of Biochemistry and Molecular Biology, Dalhousie University, Halifax, Nova Scotia, CanadaIntegrated Microbial Biodiversity Program, Canadian Institute for Advanced Research, Halifax, Nova Scotia, Canada.
700    1_
$a Eliáš, Marek $u Department of Biology and Ecology, Faculty of Science, University of Ostrava, Czech Republic marek.elias@osu.cz.
773    0_
$w MED00170504 $t Genome biology and evolution $x 1759-6653 $g Roč. 6, č. 8 (2014), s. 1956-61
856    41
$u https://pubmed.ncbi.nlm.nih.gov/25015079 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20150709 $b ABA008
991    __
$a 20150729122655 $b ABA008
999    __
$a ok $b bmc $g 1083603 $s 906258
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2014 $b 6 $c 8 $d 1956-61 $i 1759-6653 $m Genome biology and evolution $n Genome Biol Evol $x MED00170504
LZP    __
$a Pubmed-20150709

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...