Unassigned MURF1 of kinetoplastids codes for NADH dehydrogenase subunit 2

<p>Abstract</p> <p>Background</p> <p>In a previous study, we conducted a large-scale similarity-free function prediction of mitochondrion-encoded hypothetical proteins, by which the hypothetical gene <it>murf1 </it>(maxicircle unidentified reading frame 1) w...

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Main Authors: Burger Gertraud, Kannan Sivakumar
Format: Article
Language:English
Published: BMC 2008-10-01
Series:BMC Genomics
Online Access:http://www.biomedcentral.com/1471-2164/9/455
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spelling doaj-32302942deaa48f8b26854ff6358439c2020-11-25T00:32:48ZengBMCBMC Genomics1471-21642008-10-019145510.1186/1471-2164-9-455Unassigned MURF1 of kinetoplastids codes for NADH dehydrogenase subunit 2Burger GertraudKannan Sivakumar<p>Abstract</p> <p>Background</p> <p>In a previous study, we conducted a large-scale similarity-free function prediction of mitochondrion-encoded hypothetical proteins, by which the hypothetical gene <it>murf1 </it>(maxicircle unidentified reading frame 1) was assigned as <it>nad2</it>, encoding subunit 2 of NADH dehydrogenase (Complex I of the respiratory chain). This hypothetical gene occurs in the mitochondrial genome of kinetoplastids, a group of unicellular eukaryotes including the causative agents of African sleeping sickness and leishmaniasis. In the present study, we test this assignment by using bioinformatics methods that are highly sensitive in identifying remote homologs and confront the prediction with available biological knowledge.</p> <p>Results</p> <p>Comparison of MURF1 profile Hidden Markov Model (HMM) against function-known profile HMMs in Pfam, Panther and TIGR shows that MURF1 is a Complex I protein, but without specifying the exact subunit. Therefore, we constructed profile HMMs for each individual subunit, using all available sequences clustered at various identity thresholds. HMM-HMM comparison of these individual NADH subunits against MURF1 clearly identifies this hypothetical protein as NAD2. Further, we collected the relevant experimental information about kinetoplastids, which provides additional evidence in support of this prediction.</p> <p>Conclusion</p> <p>Our <it>in silico </it>analyses provide convincing evidence for MURF1 being a highly divergent member of NAD2.</p> http://www.biomedcentral.com/1471-2164/9/455
collection DOAJ
language English
format Article
sources DOAJ
author Burger Gertraud
Kannan Sivakumar
spellingShingle Burger Gertraud
Kannan Sivakumar
Unassigned MURF1 of kinetoplastids codes for NADH dehydrogenase subunit 2
BMC Genomics
author_facet Burger Gertraud
Kannan Sivakumar
author_sort Burger Gertraud
title Unassigned MURF1 of kinetoplastids codes for NADH dehydrogenase subunit 2
title_short Unassigned MURF1 of kinetoplastids codes for NADH dehydrogenase subunit 2
title_full Unassigned MURF1 of kinetoplastids codes for NADH dehydrogenase subunit 2
title_fullStr Unassigned MURF1 of kinetoplastids codes for NADH dehydrogenase subunit 2
title_full_unstemmed Unassigned MURF1 of kinetoplastids codes for NADH dehydrogenase subunit 2
title_sort unassigned murf1 of kinetoplastids codes for nadh dehydrogenase subunit 2
publisher BMC
series BMC Genomics
issn 1471-2164
publishDate 2008-10-01
description <p>Abstract</p> <p>Background</p> <p>In a previous study, we conducted a large-scale similarity-free function prediction of mitochondrion-encoded hypothetical proteins, by which the hypothetical gene <it>murf1 </it>(maxicircle unidentified reading frame 1) was assigned as <it>nad2</it>, encoding subunit 2 of NADH dehydrogenase (Complex I of the respiratory chain). This hypothetical gene occurs in the mitochondrial genome of kinetoplastids, a group of unicellular eukaryotes including the causative agents of African sleeping sickness and leishmaniasis. In the present study, we test this assignment by using bioinformatics methods that are highly sensitive in identifying remote homologs and confront the prediction with available biological knowledge.</p> <p>Results</p> <p>Comparison of MURF1 profile Hidden Markov Model (HMM) against function-known profile HMMs in Pfam, Panther and TIGR shows that MURF1 is a Complex I protein, but without specifying the exact subunit. Therefore, we constructed profile HMMs for each individual subunit, using all available sequences clustered at various identity thresholds. HMM-HMM comparison of these individual NADH subunits against MURF1 clearly identifies this hypothetical protein as NAD2. Further, we collected the relevant experimental information about kinetoplastids, which provides additional evidence in support of this prediction.</p> <p>Conclusion</p> <p>Our <it>in silico </it>analyses provide convincing evidence for MURF1 being a highly divergent member of NAD2.</p>
url http://www.biomedcentral.com/1471-2164/9/455
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