Evolutionary and biochemical analyses reveal conservation of the Brassicaceae telomerase ribonucleoprotein complex.

The telomerase ribonucleoprotein complex (RNP) is essential for genome stability and performs this role through the addition of repetitive DNA to the ends of chromosomes. The telomerase enzyme is composed of a reverse transcriptase (TERT), which utilizes a template domain in an RNA subunit (TER) to...

Full description

Bibliographic Details
Main Authors: Kelly Dew-Budd, Julie Cheung, Kyle Palos, Evan S Forsythe, Mark A Beilstein
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2020-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0222687
_version_ 1818588012021284864
author Kelly Dew-Budd
Julie Cheung
Kyle Palos
Evan S Forsythe
Mark A Beilstein
author_facet Kelly Dew-Budd
Julie Cheung
Kyle Palos
Evan S Forsythe
Mark A Beilstein
author_sort Kelly Dew-Budd
collection DOAJ
description The telomerase ribonucleoprotein complex (RNP) is essential for genome stability and performs this role through the addition of repetitive DNA to the ends of chromosomes. The telomerase enzyme is composed of a reverse transcriptase (TERT), which utilizes a template domain in an RNA subunit (TER) to reiteratively add telomeric DNA at the ends of chromosomes. Multiple TERs have been identified in the model plant Arabidopsis thaliana. Here we combine a phylogenetic and biochemical approach to understand how the telomerase RNP has evolved in Brassicaceae, the family that includes A. thaliana. Because of the complex phylogenetic pattern of template domain loss and alteration at the previously characterized A. thaliana TER loci, TER1 and TER2, across the plant family Brassicaceae, we bred double mutants from plants with a template deletion at AtTER1 and T-DNA insertion at AtTER2. These double mutants exhibited no telomere length deficiency, a definitive indication that neither of these loci encode a functional telomerase RNA. Moreover, we determined that the telomerase components TERT, Dyskerin, and the KU heterodimer are under strong purifying selection, consistent with the idea that the TER with which they interact is also conserved. To test this hypothesis further, we analyzed the substrate specificity of telomerase from species across Brassicaceae and determined that telomerase from close relatives bind and extend substrates in a similar manner, supporting the idea that TERs in different species are highly similar to one another and are likely encoded from an orthologous locus. Lastly, TERT proteins from across Brassicaceae were able to complement loss of function tert mutants in vivo, indicating TERTs from other species have the ability to recognize the native TER of A. thaliana. Finally, we immunoprecipitated the telomerase complex and identified associated RNAs via RNA-seq. Using our evolutionary data we constrained our analyses to conserved RNAs within Brassicaceae that contained a template domain. These analyses revealed a highly expressed locus whose disruption by a T-DNA resulted in a telomeric phenotype similar to the loss of other telomerase core proteins, indicating that the RNA has an important function in telomere maintenance.
first_indexed 2024-12-16T09:17:59Z
format Article
id doaj.art-ff7892c7bb794588a12f0ded9a5ca687
institution Directory Open Access Journal
issn 1932-6203
language English
last_indexed 2024-12-16T09:17:59Z
publishDate 2020-01-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS ONE
spelling doaj.art-ff7892c7bb794588a12f0ded9a5ca6872022-12-21T22:36:51ZengPublic Library of Science (PLoS)PLoS ONE1932-62032020-01-01154e022268710.1371/journal.pone.0222687Evolutionary and biochemical analyses reveal conservation of the Brassicaceae telomerase ribonucleoprotein complex.Kelly Dew-BuddJulie CheungKyle PalosEvan S ForsytheMark A BeilsteinThe telomerase ribonucleoprotein complex (RNP) is essential for genome stability and performs this role through the addition of repetitive DNA to the ends of chromosomes. The telomerase enzyme is composed of a reverse transcriptase (TERT), which utilizes a template domain in an RNA subunit (TER) to reiteratively add telomeric DNA at the ends of chromosomes. Multiple TERs have been identified in the model plant Arabidopsis thaliana. Here we combine a phylogenetic and biochemical approach to understand how the telomerase RNP has evolved in Brassicaceae, the family that includes A. thaliana. Because of the complex phylogenetic pattern of template domain loss and alteration at the previously characterized A. thaliana TER loci, TER1 and TER2, across the plant family Brassicaceae, we bred double mutants from plants with a template deletion at AtTER1 and T-DNA insertion at AtTER2. These double mutants exhibited no telomere length deficiency, a definitive indication that neither of these loci encode a functional telomerase RNA. Moreover, we determined that the telomerase components TERT, Dyskerin, and the KU heterodimer are under strong purifying selection, consistent with the idea that the TER with which they interact is also conserved. To test this hypothesis further, we analyzed the substrate specificity of telomerase from species across Brassicaceae and determined that telomerase from close relatives bind and extend substrates in a similar manner, supporting the idea that TERs in different species are highly similar to one another and are likely encoded from an orthologous locus. Lastly, TERT proteins from across Brassicaceae were able to complement loss of function tert mutants in vivo, indicating TERTs from other species have the ability to recognize the native TER of A. thaliana. Finally, we immunoprecipitated the telomerase complex and identified associated RNAs via RNA-seq. Using our evolutionary data we constrained our analyses to conserved RNAs within Brassicaceae that contained a template domain. These analyses revealed a highly expressed locus whose disruption by a T-DNA resulted in a telomeric phenotype similar to the loss of other telomerase core proteins, indicating that the RNA has an important function in telomere maintenance.https://doi.org/10.1371/journal.pone.0222687
spellingShingle Kelly Dew-Budd
Julie Cheung
Kyle Palos
Evan S Forsythe
Mark A Beilstein
Evolutionary and biochemical analyses reveal conservation of the Brassicaceae telomerase ribonucleoprotein complex.
PLoS ONE
title Evolutionary and biochemical analyses reveal conservation of the Brassicaceae telomerase ribonucleoprotein complex.
title_full Evolutionary and biochemical analyses reveal conservation of the Brassicaceae telomerase ribonucleoprotein complex.
title_fullStr Evolutionary and biochemical analyses reveal conservation of the Brassicaceae telomerase ribonucleoprotein complex.
title_full_unstemmed Evolutionary and biochemical analyses reveal conservation of the Brassicaceae telomerase ribonucleoprotein complex.
title_short Evolutionary and biochemical analyses reveal conservation of the Brassicaceae telomerase ribonucleoprotein complex.
title_sort evolutionary and biochemical analyses reveal conservation of the brassicaceae telomerase ribonucleoprotein complex
url https://doi.org/10.1371/journal.pone.0222687
work_keys_str_mv AT kellydewbudd evolutionaryandbiochemicalanalysesrevealconservationofthebrassicaceaetelomeraseribonucleoproteincomplex
AT juliecheung evolutionaryandbiochemicalanalysesrevealconservationofthebrassicaceaetelomeraseribonucleoproteincomplex
AT kylepalos evolutionaryandbiochemicalanalysesrevealconservationofthebrassicaceaetelomeraseribonucleoproteincomplex
AT evansforsythe evolutionaryandbiochemicalanalysesrevealconservationofthebrassicaceaetelomeraseribonucleoproteincomplex
AT markabeilstein evolutionaryandbiochemicalanalysesrevealconservationofthebrassicaceaetelomeraseribonucleoproteincomplex