| Diplonemidae | |
|---|---|
 | |
| Diplonema papillatum | |
Scientific classification | |
| Domain: | Eukaryota |
| Clade: | Discoba |
| Phylum: | Euglenozoa |
| Subphylum: | Glycomonada |
| Class: | Diplonemea |
| Order: | Diplonemida |
| Family: | Diplonemidae Lukeš, Julius; Flegontova, Olga; Horák, Aleš (2015). |
| Genera | |
| Synonyms | |
| |
Diplonemidae is a family of biflagellated unicellular protists that may be among the more diverse and common groups of planktonic organisms in the ocean. Although this family is currently made up of three named genera;Diplonema,Rhynchopus, andHemistasia, there likely exist thousands of still unnamed genera.[1] Organisms are generally colourless and oblong in shape, with two flagella emerging from a subapical pocket.[2] They possess a large mitochondrial genome composed of fragmented linear DNA.[3] These non-coding sequences must be massively trans-spliced, making it one of the most complicated post-transcriptional editing process known to eukaryotes.
The word "Diplonemidae" come from the Greek words 'diplo', meaning two, and 'nemat', meaning thread. Together, Diplonemidae roughly translates to 'two threads', likely referring to the characteristic two flagella of the organism.
Primary studies done in the 1900s by Griessmann and Skuja had initially grouped Diplonemidae (or more specifically, theDiplonema andRhynchopus taxa) with the euglenids. This was due to the two groups sharing many morphological similarities with theeuglenids, such as metaboly, locomotion and a microtubule-reinforced feeding apparatus.[4] However, this conclusion was met with some controversy, as diplonemids lacked characteristic features shared by all euglenids, such as possession of pellicle strips and paraxonemal rods on their flagella.[5] Instead, they were placed in the euglenozoan phylum and shared this taxon with the kinetoplastids and euglenids.[6] The inclusion ofRhynchopus andDiplonema in the family Diplonemidae was later confirmed through nuclear 18S rRNA analysis.[7] As of now,Rhynchopus andDiplonema are part of the 'classical' diplonemid subgroup, andHemistasia is part of the 'nonclassical' diplonemid subgroup.
Recently, there had been debates as to whether Diplonemidae were more closely related to theeuglenids orkinetoplastids. It was not until analysis of cytosolic heat shock proteins that a sister relationship between the diplonemids and kinetoplastids was proposed.[5] This was further supported through phylogenetic analysis, which discovered that Diplonemidae possess a functional splice leader RNA that is characteristic of the kinetoplastids.[8] Additionally, the amino acid tryptophan is encoded by codon TGA in kinetoplastids and diplonemids, whereas in euglenids, the regular codon is used instead.[5]
Nevertheless, despite the similarities between kinetoplastids and diplonemids, the two taxa are still distinct from each other. Diplonemidae still lack a kinetoplast, and have a unique bi-flagellated trophic phase not seen in kinetoplastids. Presently, the kinetoplastids are regarded as the sister group to the Diplonemidae.
Although there are only three named genera within the Diplonemidae, environmental sequencing performed by the recent TARA Ocean Expedition concluded there are potentially thousands of genera,[1] suggesting that pelagic Diplonemidae are the most diverse planktonic eukaryotes in the oceans.
Although Diplonemidae are generally predators, some species display parasitic life strategies.[3] Diplonemidae display a rich diversity in marine and freshwater environments, with their relative abundance increasing with depth.[9] The diplonemids that exist in these different environments are genetically distinct, and exhibit slightly different lifestyles. The 'classic' diplonemids (i.e.Diplonema andRhynchopus) are benthic, whereas the marine diplonemids, which includeHemistasia, are planktonic.[2]
There are potentially thousands of unknown marine Diplonemidae species, with this diversity highly stratified in accordance to depth. Although molecular sequencing confirms the existence of these unnamed marine Diplonemidae, information regarding their morphology and lifestyle is absent.[1] As marine Diplonemidae are the most abundant and genetically diverse protists (and potentially eukaryotes) in the sea, there are strong implications that they play a key role in aquatic ecosystems. As of now, this exact role is unknown.
Classical diplonemids (i.e.Diplonema andRhynchopus), are colourless and oblong in shape. They are approximately 20 μm in length and possess a microtubule layer underneath their plasma membrane.[10] Adjacent to it is a mitochondrion with discoidal cristae.[6] They also possess two flagella of equal length, both of which lack paraxial rods.[2] The two basal bodies originate from a subapical pocket, which merges with an adjacent feeding apparatus.[4] This feeding apparatus is surrounded by many food vacuoles and reinforced by microtubules.[10]
Nonclassical Diplonemidae (i.e.Hemistasia) are diverse in size but share many morphological aspects with the classic diplonemids. However, a great majority of these marine Diplonemidae have never been seen, with their existence only confirmed through molecular analysis.[2]
Although Diplonemidae do not possess pellicular strips likeeuglenids, they still move via metaboly.[3]
Diplonemidae also exhibit the compartmentalization of glycolytic and gluconeogenic enzymes into peroxisomes. These organelles are referred to as glycosomes, and is a characteristic feature also shared with their sister taxon, thekinetoplastids.[11]
Diplonemidae are capable of sexual reproduction, as genes involved in meiosis have been found.[12] Although marine diplonemids appear to reproduce sexually, not much is known about diplonemid reproduction asEuglenozoans rarely demonstrate sexual processes.[5]
Diplonemidae have a unique mitochondrial DNA arrangement. Although Diplonemidae possess a large mitochondrial genome, these do not contain any intact full-sized genes. Instead, their mitochondrial DNA consists of linear gene fragments of different sizes. Because each fragment is both full of repeats and incomplete, individually they are unable to code for a gene themselves. Instead, fragments are transcribed and spliced together using their own specialized trans splicing machinery.[3] Once spliced together, the transcript undergoes extensive editing to become recognizable RNA. This is accomplished by either Uracil-insertion, nucleotide deanimation, or substitution, which eventually generates a fully mature and translatable transcript.[13]
The Diplonemidae genome contains a spliced leader RNA gene, which confirms their use of mRNA spliceosome-dependent trans splicing during nuclear expression.
Diplonemids possess thegap3 gene which is specifically found incyanobacteria andPseudomonadota. This is likely due to lateral gene transfer following the divergence of diplonemids from the euglenoids.[14] As to date, this is one of the most-supported examples of lateral gene transfer from a bacterium to eukaryote and may have implications for diplonemid acquisition of biochemical abilities.
Although presently made up of less than a dozen named species, the existence of thousands of unknown diplonemid taxa has been suggested through environmental sequencing analyses.[1]