@ARTICLE{TreeBASE2Ref23016,
author = {Francisco Jose Sanchez-Luque and Manuel Carlos Lopez and Patricia Eugenia Carreira and Carlos Alonso and Mar?a Carmen Thomas},
title = {The wide expansion of Hepatitis Delta Virus-like ribozymes throughout trypanosomatid genomes is linked to the spreading of L1Tc/ingi clade mobile elements.},
year = {2014},
keywords = {Retrotransposon, LINE, SINE, HDV-like ribozyme, Pr77, Trypanosoma, Leishmania, L1Tc, SIDER, ingi },
doi = {},
url = {http://},
pmid = {},
journal = {BMC Genomics},
volume = {},
number = {},
pages = {},
abstract = {BACKGROUND: Hepatitis Delta Virus (HDV)-like ribozymes have recently been found in many mobile elements in which they take part in a mechanism that releases intermediate RNAs from cellular co-transcripts. L1Tc in Trypanosoma cruzi is one of the elements in which such a ribozyme is located. It lies in the so-called Pr77-hallmark, a conserved region shared by retrotransposons belonging to the trypanosomatid L1Tc/ingi clade. The wide distribution of the Pr77-hallmark detected in trypanosomatid retrotransposons renders the potential catalytic activity of these elements worthy of study: their distribution might contribute to host genetic regulation at the mRNA level. Indeed, in Leishmania spp, the pervasive presence of these HDV-like ribozyme-containing mobile elements in certain 3?-untranslated regions of protein-coding genes has been linked to mRNA downregulation.
RESULTS: Intensive screening of publicly available trypanosomatid genomes, combined with manual folding analyses, allowed the isolation of putatively Pr77-hallmarks with HDV-like ribozyme activity. This work describes the conservation of an HDV-like ribozyme structure in the Pr77 sequence of retrotransposons in a wide range of trypanosomatids, the catalytic function of which is maintained in the majority. These results are consistent with the previously suggested common phylogenetic origin of the elements that belong to this clade, although in some cases loss of functionality appears to have occurred and/or perhaps molecular domestication by the host.
CONCLUSIONS: These HDV-like ribozymes are widely distributed within retrotransposons across trypanosomatid genomes. This type of ribozyme was once thought to be rare in nature, but in fact it would seem to be abundant in trypanosomatid transcripts. It can even form part of the pool of mRNA 3'-untranslated regions, particularly in Leishmania spp. Its putative regulatory role in host genetic expression is discussed.}
}
Taxa for tree 74359 of Study 15572

Citation title:
"The wide expansion of Hepatitis Delta Virus-like ribozymes throughout trypanosomatid genomes is linked to the spreading of L1Tc/ingi clade mobile elements.".

Study name:
"The wide expansion of Hepatitis Delta Virus-like ribozymes throughout trypanosomatid genomes is linked to the spreading of L1Tc/ingi clade mobile elements.".

This study is part of submission 15572
(Status: Published).
Taxa
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ID |
Taxon Label |
NCBI taxid |
uBIO namebankID |
1467196 |
Drosophila willistoni R2 SIDE |
7260
|
2615038
|
1467217 |
Leishmania braziliensis M28 836014 |
5660
|
5434552
|
1467211 |
Leishmania donovani 20 v01s1 1036612 |
5661
|
4939840
|
1467216 |
Leishmania donovani 28 v01s1 832468 |
5661
|
4939840
|
1467214 |
Leishmania infantum J28 828417 |
38573
|
4939837
|
1467213 |
Leishmania infantum J29 1017989 |
38573
|
4939837
|
1467197 |
Leishmania major F28 813783 |
5664
|
4939843
|
1467220 |
Leishmania major F29 1010562 |
5664
|
4939843
|
1467219 |
Leishmania mexicana M08 29 190165 |
5665
|
5432993
|
1467209 |
Leishmania mexicana M28 803106 |
5665
|
5432993
|
1467215 |
Leishmania panamensis KB453284 328629 |
5679
|
5472637
|
1467226 |
Leishmania panamensis KB453339 66838 |
5679
|
5472637
|
1467210 |
Leishmania tarentolae P28 804618 |
5689
|
5461533
|
1467224 |
Leishmania tarentolae P29 986367 |
5689
|
5461533
|
1467188 |
Trypanosoma brucei Tb427 03 v4 6279 |
5691
|
5327167
|
1467191 |
Trypanosoma brucei Tb427 09 v4 3011406 |
5691
|
5327167
|
1467198 |
Trypanosoma brucei Tb427 10 v5 452323 |
5691
|
5327167
|
1467189 |
Trypanosoma brucei Tb427 11 01 v4 4593961 |
5691
|
5327167
|
1467199 |
Trypanosoma brucei Tb927 03 v4 5793 |
5691
|
5327167
|
1467203 |
Trypanosoma brucei Tb927 04 v4 1473651 |
5691
|
5327167
|
1467200 |
Trypanosoma brucei Tb927 06 v4 1550987 |
5691
|
5327167
|
1467193 |
Trypanosoma brucei Tb927 06 v4 1596247 |
5691
|
5327167
|
1467194 |
Trypanosoma brucei Tb927 08 v4 17261 |
5691
|
5327167
|
1467201 |
Trypanosoma brucei Tb927 09 v4 2520024 |
5691
|
5327167
|
1467222 |
Trypanosoma brucei Tb927 09 v4 3010329 |
5691
|
5327167
|
1467204 |
Trypanosoma brucei Tb927 10 v5 452220 |
5691
|
5327167
|
1467192 |
Trypanosoma brucei Tb927 11 01 v4 4592751 |
5691
|
5327167
|
1467223 |
Trypanosoma brucei Tbg927 04 1420728 |
5691
|
5327167
|
1467225 |
Trypanosoma brucei Tbg972 10 401727 |
5691
|
5327167
|
1467195 |
Trypanosoma congolense bin 13361355 |
5692
|
5436893
|
1467187 |
Trypanosoma congolense bin 7431359 |
5692
|
5436893
|
1467202 |
Trypanosoma congolense pschr 1 110891 |
5692
|
5436893
|
1467221 |
Trypanosoma congolense pschr 1 117249 |
5692
|
5436893
|
1467190 |
Trypanosoma congolense pschr 10 2982978 |
5692
|
5436893
|
1467218 |
Trypanosoma congolense pschr 10 400469 |
5692
|
5436893
|
1467205 |
Trypanosoma congolense pschr 11 3750506 |
5692
|
5436893
|
1467212 |
Trypanosoma congolense pschr 3 45521 |
5692
|
5436893
|
1467208 |
Trypanosoma congolense pschr 5 603310 |
5692
|
5436893
|
1467206 |
Trypanosoma vivax Y486 bin 11221740 |
5699
|
5435492
|
1467207 |
Trypanosoma vivax Y489 03 1238673 |
5699
|
5435492
|