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Xenopus
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<h2 id="characteristics">Characteristics</h2> <p><i>Xenopus laevis</i> is a rather inactive creature. It is incredibly hardy and can live up to 15 years. At times the ponds that <i>Xenopus laevis</i> is found in dry up, compelling it, in the dry season, to burrow into the mud, leaving a tunnel for air. It may lie dormant for up to a year. If the pond dries up in the rainy season, <i>Xenopus laevis</i> may migrate long distances to another pond, maintaining hydration by the rains. It is an adept swimmer, swimming in all directions with ease. It is barely able to hop, but it is able to crawl. It spends most of its time underwater and comes to surface to breathe. Respiration is predominantly through its well-developed lungs; there is little cutaneous respiration. </p> <h3>Description</h3> <p>All species of <i>Xenopus</i> have flattened, somewhat egg-shaped and streamlined bodies, and very slippery skin (because of a protective mucus covering).<a class="footnote-ref" id="fnref:6" href="#fn:6"><sup>6</sup></a> The frog's skin is smooth, but with a <a href="/facts/Lateral_line/u88dwyxh">lateral line</a> sensory organ that has a stitch-like appearance. The frogs are all excellent swimmers and have powerful, fully webbed toes, though the fingers lack webbing. Three of the toes on each foot have conspicuous black <a href="/facts/Claw/s9WKKWAv">claws</a>. </p><p>The frog's eyes are on top of the head, looking upwards. The <a href="/facts/Pupils/E4ec4lfJ">pupils</a> are circular. They have no moveable <a href="/facts/Eyelids/w4b7fJGm">eyelids</a>, <a href="/facts/Tongue/oW4tp3a0">tongues</a> (rather it is completely attached to the floor of the mouth<a class="footnote-ref" id="fnref:7" href="#fn:7"><sup>7</sup></a>) or <a href="/facts/Eardrum/2mHLYSMF">eardrums</a> (similarly to <a href="/facts/Common_Suriname_toad/T4U36CnY"><i>Pipa pipa</i>, the common Suriname toad</a><a class="footnote-ref" id="fnref:8" href="#fn:8"><sup>8</sup></a>).<a class="footnote-ref" id="fnref:9" href="#fn:9"><sup>9</sup></a> </p><p>Unlike most amphibians, they have no <a href="/facts/Haptoglobin/FvX19ch9">haptoglobin</a> in their <a href="/facts/Blood/03zEulkj">blood</a>.<a class="footnote-ref" id="fnref:10" href="#fn:10"><sup>10</sup></a> </p> <h3>Behaviour</h3> <p><i>Xenopus</i> species are entirely <a href="/facts/Aquatic_animal/tY7gyRWl">aquatic</a>, though they have been observed migrating on land to nearby bodies of water during times of <a href="/facts/Drought/LVW0rfuV">drought</a> or in heavy rain. They are usually found in <a href="/facts/Lake/YP0xxn0E">lakes</a>, <a href="/facts/River/GP7MSur6">rivers</a>, <a href="/facts/Swamps/rjE9QKpm">swamps</a>, potholes in streams, and man-made reservoirs.<a class="footnote-ref" id="fnref:11" href="#fn:11"><sup>11</sup></a> </p><p>Adult frogs are usually both <a href="/facts/Predator/JEGdrX3f">predators</a> and <a href="/facts/Scavengers/rfMKhUmh">scavengers</a>, and since their tongues are unusable, the frogs use their small fore limbs to aid in the feeding process. Since they also lack <a href="/facts/Vocal_sac/0J9nCqJQ">vocal sacs</a>, they make clicks (brief pulses of sound) underwater (again similar to <i><a href="/facts/Pipa_pipa/T4U36CnY">Pipa pipa</a></i>).<a class="footnote-ref" id="fnref:12" href="#fn:12"><sup>12</sup></a> Males establish a hierarchy of social dominance in which primarily one male has the right to make the advertisement call.<a class="footnote-ref" id="fnref:13" href="#fn:13"><sup>13</sup></a> The females of many species produce a release call, and <i><a href="/facts/Xenopus_laevis/khG1KPrd">Xenopus laevis</a></i> females produce an additional call when sexually receptive and soon to lay eggs.<a class="footnote-ref" id="fnref:14" href="#fn:14"><sup>14</sup></a> The <i>Xenopus</i> species are also active during the twilight (or <a href="/facts/Crepuscular/nHEUNhSo">crepuscular</a>) hours.<a class="footnote-ref" id="fnref:15" href="#fn:15"><sup>15</sup></a> </p><p>During breeding season, the males develop ridge-like nuptial pads (black in color) on their fingers to aid in grasping the female. The frogs' mating embrace is inguinal, meaning the male grasps the female around her waist.<a class="footnote-ref" id="fnref:16" href="#fn:16"><sup>16</sup></a> </p> <h2 id="species">Species</h2> <h3>Extant species</h3> <ul><li><i><a href="/facts/Xenopus_allofraseri/yz8F2F4d">Xenopus allofraseri</a></i></li> <li><i><a href="/facts/Xenopus_amieti/hBCwTXk9">Xenopus amieti</a></i> (<a href="/facts/Volcano_clawed_frog/hBCwTXk9">volcano clawed frog</a>)</li> <li><i><a href="/facts/Xenopus_andrei/GLnqAmNM">Xenopus andrei</a></i> (<a href="/facts/Andre%2527s_clawed_frog/GLnqAmNM">Andre's clawed frog</a>)</li> <li><i><a href="/facts/Xenopus_borealis/fomUhees">Xenopus borealis</a></i> (<a href="/facts/Marsabit_clawed_frog/fomUhees">Marsabit clawed frog</a>)</li> <li><i><a href="/facts/Xenopus_boumbaensis/HyTwVatQ">Xenopus boumbaensis</a></i> (<a href="/facts/Mawa_clawed_frog/HyTwVatQ">Mawa clawed frog</a>)</li> <li><i><a href="/facts/Xenopus_calcaratus/PPXxxtWE">Xenopus calcaratus</a></i></li> <li><i><a href="/facts/Xenopus_clivii/DFmBepYJ">Xenopus clivii</a></i> (<a href="/facts/Eritrea_clawed_frog/DFmBepYJ">Eritrea clawed frog</a>)</li> <li><i><a href="/facts/Xenopus_epitropicalis/LWKwQCh8">Xenopus epitropicalis</a></i> (<a href="/facts/Cameroon_clawed_frog/LWKwQCh8">Cameroon clawed frog</a>)</li> <li><i><a href="/facts/Xenopus_eysoole/JBle5U5E">Xenopus eysoole</a></i></li> <li><i><a href="/facts/Xenopus_fischbergi/66PSLt6e">Xenopus fischbergi</a></i></li> <li><i><a href="/facts/Xenopus_fraseri/t0vK1g9p">Xenopus fraseri</a></i> (<a href="/facts/Fraser%2527s_platanna/t0vK1g9p">Fraser's platanna</a>)</li> <li><i><a href="/facts/Xenopus_gilli/RRJSmLus">Xenopus gilli</a></i> (<a href="/facts/Cape_platanna/RRJSmLus">Cape platanna</a>)</li> <li><i><a href="/facts/Xenopus_itombwensis/60P9BGm6">Xenopus itombwensis</a></i></li> <li><i><a href="/facts/Xenopus_kobeli/dpPslEBt">Xenopus kobeli</a></i></li> <li><i><a href="/facts/Xenopus_laevis/khG1KPrd">Xenopus laevis</a></i> (<a href="/facts/African_clawed_frog/khG1KPrd">African clawed frog</a> or common platanna)</li> <li><i><a href="/facts/Xenopus_largeni/xTpmrXcm">Xenopus largeni</a></i> (<a href="/facts/Largen%2527s_clawed_frog/xTpmrXcm">Largen's clawed frog</a>)</li> <li><i><a href="/facts/Xenopus_lenduensis/d86IAQcC">Xenopus lenduensis</a></i> (<a href="/facts/Lendu_Plateau_clawed_frog/d86IAQcC">Lendu Plateau clawed frog</a>)</li> <li><i><a href="/facts/Xenopus_longipes/TWL9Pw2S">Xenopus longipes</a></i> (<a href="/facts/Lake_Oku_clawed_frog/TWL9Pw2S">Lake Oku clawed frog</a>)</li> <li><i><a href="/facts/Xenopus_mellotropicalis/XJrYLYTY">Xenopus mellotropicalis</a></i></li> <li><i><a href="/facts/Xenopus_muelleri/yJSDbvFw">Xenopus muelleri</a></i> (<a href="/facts/M%25C3%25BCller%2527s_platanna/yJSDbvFw">Müller's platanna</a>)</li> <li><i><a href="/facts/Xenopus_parafraseri/xA16v2Pa">Xenopus parafraseri</a></i></li> <li><i><a href="/facts/Xenopus_petersii/mgHzlp2H">Xenopus petersii</a></i> (<a href="/facts/Peters%2527_platanna/mgHzlp2H">Peters' platanna</a>)</li> <li><i><a href="/facts/Xenopus_poweri/AmAt7o1f">Xenopus poweri</a></i></li> <li><i><a href="/facts/Xenopus_pygmaeus/VoJdLUoJ">Xenopus pygmaeus</a></i> (<a href="/facts/Bouchia_clawed_frog/VoJdLUoJ">Bouchia clawed frog</a>)</li> <li><i><a href="/facts/Xenopus_ruwenzoriensis/9BkYM8l5">Xenopus ruwenzoriensis</a></i> (<a href="/facts/Uganda_clawed_frog/9BkYM8l5">Uganda clawed frog</a>)</li> <li><i><a href="/facts/Xenopus_tropicalis/uoS2ALeT">Xenopus tropicalis</a></i> (<a href="/facts/Western_clawed_frog/uoS2ALeT">western clawed frog</a>)</li> <li><i><a href="/facts/Xenopus_vestitus/B6n2QvMb">Xenopus vestitus</a></i> (<a href="/facts/Kivu_clawed_frog/B6n2QvMb">Kivu clawed frog</a>)</li> <li><i><a href="/facts/Xenopus_victorianus/yRRLeWDG">Xenopus victorianus</a></i> (<a href="/facts/Lake_Victoria_clawed_frog/yRRLeWDG">Lake Victoria clawed frog</a>)</li> <li><i><a href="/facts/Xenopus_wittei/xowbAKUq">Xenopus wittei</a></i> (<a href="/facts/De_Witte%2527s_clawed_frog/xowbAKUq">De Witte's clawed frog</a>)</li></ul> <h3>Fossil species</h3> <p>The following fossil species have been described:<a class="footnote-ref" id="fnref:17" href="#fn:17"><sup>17</sup></a> </p> <ul><li>†<i>Xenopus arabiensis</i> Henrici and Báez 2001 - <a href="/facts/Oligocene/n3gnNogo">Oligocene</a> Yemen Volcanic Group, Yemen</li> <li>†<i>Xenopus hasaunus</i> Spinar 1980</li> <li>†<i>Xenopus romeri</i> Estes 1975 - <a href="/facts/Itaboraian/prTnSG5m">Itaboraian</a> <a href="/facts/Itabora%25C3%25AD_Formation/XTLXlMg8">Itaboraí Formation</a>, Brazil</li> <li>†<i>Xenopus stromeri</i> Ahl 1926</li> <li><i>cf. Xenopus sp.</i> - <a href="/facts/Campanian/MoPSxcqL">Campanian</a> - <a href="/facts/Los_Alamitos_Formation/MEN1sPMY">Los Alamitos Formation</a>, Argentina</li> <li><i>Xenopus (Xenopus) sp.</i> - <a href="/facts/Late_Oligocene/WLk2kdUC">Late Oligocene</a> <a href="/facts/Nsungwe_Formation/20m9029y">Nsungwe Formation</a>, Tanzania</li> <li><i>Xenopus sp.</i> - <a href="/facts/Miocene/cBRRzq4g">Miocene</a> Morocco</li> <li><i>Xenopus sp.</i> - <a href="/facts/Early_Pleistocene/jPp2Cn7a">Early Pleistocene</a> Olduvai Formation, Tanzania</li></ul> <h2 id="model-organism-for-biological-research">Model organism for biological research</h2> <p>Like many other <a href="/facts/Frogs/IxYhbeda">frogs</a>, they are often used in laboratory as research subjects.<a class="footnote-ref" id="fnref:18" href="#fn:18"><sup>18</sup></a> <i>Xenopus</i> embryos and eggs are a popular model system for a wide variety of biological studies.<a class="footnote-ref" id="fnref:19" href="#fn:19"><sup>19</sup></a><a class="footnote-ref" id="fnref:20" href="#fn:20"><sup>20</sup></a> This animal is used because of its powerful combination of experimental tractability and close evolutionary relationship with humans, at least compared to many model organisms.<a class="footnote-ref" id="fnref:21" href="#fn:21"><sup>21</sup></a><a class="footnote-ref" id="fnref:22" href="#fn:22"><sup>22</sup></a> </p><p><i>Xenopus</i> has long been an important tool for <i>in vivo studies</i> in molecular, cell, and developmental biology of vertebrate animals.<a class="footnote-ref" id="fnref:23" href="#fn:23"><sup>23</sup></a> However, the wide breadth of <i>Xenopus</i> research stems from the additional fact that <a href="/facts/Cell-free_system/Tow6j88h">cell-free extracts</a> made from <i>Xenopus</i> are a premier <i>in vitro </i>system for studies of fundamental aspects of cell and molecular biology. Thus, <i>Xenopus</i> is a vertebrate model system that allows for high-throughput <i>in vivo</i> analyses of gene function and high-throughput biochemistry. Furthermore, <i>Xenopus</i> oocytes are a leading system for studies of ion transport and channel physiology.<a class="footnote-ref" id="fnref:24" href="#fn:24"><sup>24</sup></a> <i>Xenopus</i> is also a unique system for analyses of genome evolution and whole genome duplication in vertebrates,<a class="footnote-ref" id="fnref:25" href="#fn:25"><sup>25</sup></a> as different <i>Xenopus</i> species form a <a href="/facts/Ploidy/U8zl4AQe">ploidy</a> series formed by <a href="/facts/Hybrid_(biology)/pzVJ54xU">interspecific hybridization</a>.<a class="footnote-ref" id="fnref:26" href="#fn:26"><sup>26</sup></a> </p><p>In 1931, <a href="/facts/Lancelot_Hogben/L5p5fVqY">Lancelot Hogben</a> noted that <i>Xenopus laevis</i> females ovulated when injected with the urine of pregnant women.<a class="footnote-ref" id="fnref:27" href="#fn:27"><sup>27</sup></a> This led to a pregnancy test that was later refined by South African researchers <a href="/facts/Hillel_Abbe_Shapiro/Sm204rHB">Hillel Abbe Shapiro</a> and Harry Zwarenstein.<a class="footnote-ref" id="fnref:28" href="#fn:28"><sup>28</sup></a> A female Xenopus frog injected with a woman's urine was put in a jar with a little water. If eggs were in the water a day later it meant the woman was pregnant. Four years after the first <i>Xenopus</i> test, Zwarenstein's colleague, Dr Louis Bosman, reported that the test was accurate in more than 99% of cases.<a class="footnote-ref" id="fnref:29" href="#fn:29"><sup>29</sup></a> From the 1930s to the 1950s, thousands of frogs were exported across the world for use in these pregnancy tests.<a class="footnote-ref" id="fnref:30" href="#fn:30"><sup>30</sup></a> </p><p>The National Xenopus Resource of the <a href="/facts/Marine_Biological_Laboratory/xpgyHlte">Marine Biological Laboratory</a> is an <i>in vivo</i> repository for transgenic and mutant strains and a training center.<a class="footnote-ref" id="fnref:31" href="#fn:31"><sup>31</sup></a> </p> <h3>Online Model Organism Database</h3> <p><a href="/facts/Xenbase/c2EFotmu">Xenbase</a><a class="footnote-ref" id="fnref:32" href="#fn:32"><sup>32</sup></a> is the <a href="/facts/Generic_Model_Organism_Database/gcMmv9gc">Model Organism Database (MOD)</a> for both <i><a href="/facts/Xenopus_laevis/khG1KPrd">Xenopus laevis</a></i> and <i><a href="/facts/Xenopus_tropicalis/uoS2ALeT">Xenopus tropicalis</a></i>.<a class="footnote-ref" id="fnref:33" href="#fn:33"><sup>33</sup></a> </p> <h3>Investigation of human disease genes</h3> <p>All modes of <i>Xenopus</i> research (embryos, cell-free extracts, and oocytes) are commonly used in direct studies of human disease genes and to study the basic science underlying initiation and progression of cancer.<a class="footnote-ref" id="fnref:34" href="#fn:34"><sup>34</sup></a> <i>Xenopus</i> embryos for <i>in vivo</i> studies of human disease gene function: <i>Xenopus</i> embryos are large and easily manipulated, and moreover, thousands of embryos can be obtained in a single day. Indeed, <i>Xenopus</i> was the first vertebrate animal for which methods were developed to allow rapid analysis of gene function using misexpression (by mRNA injection<a class="footnote-ref" id="fnref:35" href="#fn:35"><sup>35</sup></a>). Injection of mRNA in <i>Xenopus</i> that led to the cloning of interferon.<a class="footnote-ref" id="fnref:36" href="#fn:36"><sup>36</sup></a> Moreover, the use of morpholino-antisense oligonucleotides for gene knockdowns in vertebrate embryos, which is now widely used, was first developed by Janet Heasman using <i>Xenopus</i>.<a class="footnote-ref" id="fnref:37" href="#fn:37"><sup>37</sup></a> </p><p>In recent years, these approaches have played in important role in studies of human disease genes. The mechanism of action for several genes mutated in human cystic kidney disorders (e.g. <a href="/facts/Nephronophthisis/va6MejuB">nephronophthisis</a>) have been extensively studied in <i>Xenopus</i> embryos, shedding new light on the link between these disorders, <a href="/facts/Ciliogenesis/GwrKw6Sb">ciliogenesis</a> and <a href="/facts/Wnt_signaling/7wxpKrjy">Wnt signaling</a>.<a class="footnote-ref" id="fnref:38" href="#fn:38"><sup>38</sup></a> <i>Xenopus</i> embryos have also provided a rapid test bed for validating newly discovered disease genes. For example, studies in <i>Xenopus</i> confirmed and elucidated the role of <i>PYCR1</i> in <a href="/facts/Cutis_laxa/U5v0norU">cutis laxa</a> with progeroid features.<a class="footnote-ref" id="fnref:39" href="#fn:39"><sup>39</sup></a> </p><p>Transgenic <i>Xenopus</i> for studying transcriptional regulation of human disease genes: <i>Xenopus</i> embryos develop rapidly, so transgenesis in <i>Xenopus</i> is a rapid and effective method for analyzing genomic regulatory sequences. In a recent study, mutations in the <i>SMAD7</i> locus were revealed to associate with human <a href="/facts/Colorectal_cancer/nV592sW7">colorectal cancer</a>. The mutations lay in conserved, but noncoding sequences, suggesting these mutations impacted the patterns of <i>SMAD7</i> transcription. To test this hypothesis, the authors used <i>Xenopus</i> transgenesis, and revealed this genomic region drove expression of <a href="/facts/Green_fluorescent_protein/6nWDMhSC">GFP</a> in the hindgut. Moreover, transgenics made with the mutant version of this region displayed substantially less expression in the hindgut.<a class="footnote-ref" id="fnref:40" href="#fn:40"><sup>40</sup></a> </p><p><i>Xenopus</i> cell-free extracts for biochemical studies of proteins encoded by human disease genes: A unique advantage of the <i>Xenopus</i> system is that cytosolic extracts contain both soluble cytoplasmic and nuclear proteins (including chromatin proteins). This is in contrast to cellular extracts prepared from somatic cells with already distinct cellular compartments. <i>Xenopus</i> egg extracts have provided numerous insights into the basic biology of cells with particular impact on cell division and the DNA transactions associated with it (see below). </p><p>Studies in <i>Xenopus</i> egg extracts have also yielded critical insights into the mechanism of action of human disease genes associated with genetic instability and elevated cancer risk, such as ataxia telangiectasia, <i><a href="/facts/BRCA1/xHDwxARA">BRCA1</a></i> inherited breast and ovarian cancer, <i>Nbs1</i> Nijmegen breakage syndrome, <i>RecQL4</i> Rothmund-Thomson syndrome, <i><a href="/facts/C-Myc/7FGlAtFk">c-Myc</a></i> oncogene and FANC proteins (<a href="/facts/Fanconi_anemia/4p1QUprP">Fanconi anemia</a>).<a class="footnote-ref" id="fnref:41" href="#fn:41"><sup>41</sup></a><a class="footnote-ref" id="fnref:42" href="#fn:42"><sup>42</sup></a><a class="footnote-ref" id="fnref:43" href="#fn:43"><sup>43</sup></a><a class="footnote-ref" id="fnref:44" href="#fn:44"><sup>44</sup></a><a class="footnote-ref" id="fnref:45" href="#fn:45"><sup>45</sup></a> </p><p><i>Xenopus</i> oocytes for studies of gene expression and channel activity related to human disease: Yet another strength of <i>Xenopus</i> is the ability to rapidly and easily assay the activity of channel and transporter proteins using expression in oocytes. This application has also led to important insights into human disease, including studies related to <a href="/facts/Trypanosomatid/grHCxswB">trypanosome</a> transmission,<a class="footnote-ref" id="fnref:46" href="#fn:46"><sup>46</sup></a> <a href="/facts/Epilepsy/wawyp56a">Epilepsy</a> with <a href="/facts/Ataxia/suENWGS6">ataxia</a> and <a href="/facts/Sensorineural_deafness/wa81Kykf">sensorineural deafness</a><a class="footnote-ref" id="fnref:47" href="#fn:47"><sup>47</sup></a> Catastrophic <a href="/facts/Cardiac_arrhythmia/ooEpr46Q">cardiac arrhythmia</a> (<a href="/facts/Long-QT_syndrome/kX1NAAUh">Long-QT syndrome</a>)<a class="footnote-ref" id="fnref:48" href="#fn:48"><sup>48</sup></a> and Megalencephalic leukoencephalopathy.<a class="footnote-ref" id="fnref:49" href="#fn:49"><sup>49</sup></a> </p><p>Gene editing by the CRISPR/CAS system has recently been demonstrated in <i>Xenopus</i> <i>tropicalis</i><a class="footnote-ref" id="fnref:50" href="#fn:50"><sup>50</sup></a><a class="footnote-ref" id="fnref:51" href="#fn:51"><sup>51</sup></a> and <i>Xenopus laevis</i>.<a class="footnote-ref" id="fnref:52" href="#fn:52"><sup>52</sup></a> This technique is being used to screen the effects of human disease genes in <i>Xenopus</i> and the system is sufficiently efficient to study the effects within the same embryos that have been manipulated.<a class="footnote-ref" id="fnref:53" href="#fn:53"><sup>53</sup></a> </p> <h3>Investigation of fundamental biological processes</h3> <p><a href="/facts/Signal_transduction/1bs0Me6w">Signal transduction</a>: <i>Xenopus</i> embryos and cell-free extracts are widely used for basic research in signal transduction. In just the last few years, <i>Xenopus</i> embryos have provided crucial insights into the mechanisms of TGF-beta and Wnt signal transduction. For example, <i>Xenopus</i> embryos were used to identify the enzymes that control ubiquitination of Smad4,<a class="footnote-ref" id="fnref:54" href="#fn:54"><sup>54</sup></a> and to demonstrate direct links between TGF-beta superfamily signaling pathways and other important networks, such as the MAP kinase pathway<a class="footnote-ref" id="fnref:55" href="#fn:55"><sup>55</sup></a> and the Wnt pathway.<a class="footnote-ref" id="fnref:56" href="#fn:56"><sup>56</sup></a> Moreover, new methods using egg extracts revealed novel, important targets of the Wnt/GSK3 destruction complex.<a class="footnote-ref" id="fnref:57" href="#fn:57"><sup>57</sup></a> </p><p><a href="/facts/Cell_division/n5MrunWj">Cell division</a>: <i>Xenopus</i> egg extracts have allowed the study of many complicated cellular events <i>in vitro</i>. Because egg cytosol can support successive cycling between mitosis and interphase <i>in vitro</i>, it has been critical to diverse studies of cell division. For example, the small GTPase Ran was first found to regulate interphase nuclear transport, but <i>Xenopus</i> egg extracts revealed the critical role of Ran GTPase in mitosis independent of its role in interphase nuclear transport.<a class="footnote-ref" id="fnref:58" href="#fn:58"><sup>58</sup></a> Similarly, the cell-free extracts were used to model nuclear envelope assembly from chromatin, revealing the function of RanGTPase in regulating nuclear envelope reassembly after mitosis.<a class="footnote-ref" id="fnref:59" href="#fn:59"><sup>59</sup></a> More recently, using <i>Xenopus</i> egg extracts, it was possible to demonstrate the mitosis-specific function of the nuclear lamin B in regulating spindle morphogenesis<a class="footnote-ref" id="fnref:60" href="#fn:60"><sup>60</sup></a> and to identify new proteins that mediate kinetochore attachment to microtubules.<a class="footnote-ref" id="fnref:61" href="#fn:61"><sup>61</sup></a> <a href="/facts/Cell-free_system/Tow6j88h">Cell-free systems</a> have recently become practical investigatory tools, and <i>Xenopus</i> oocytes are often the source of the extracts used. This has produced significant results in understanding <a href="/facts/Mitotic/ExxrSUs8">mitotic</a> oscillation and <a href="/facts/Microtubule/ENL1TxSe">microtubules</a>.<a class="footnote-ref" id="fnref:62" href="#fn:62"><sup>62</sup></a> </p><p><a href="/facts/Embryonic_development/1lFY4EoW">Embryonic development</a>: <i>Xenopus</i> embryos are widely used in developmental biology. A summary of recent advances made by <i>Xenopus</i> research in recent years would include: </p> <ol><li><a href="/facts/Epigenetics/UfAAERcn">Epigenetics</a> of cell fate specification<a class="footnote-ref" id="fnref:63" href="#fn:63"><sup>63</sup></a> and epigenome reference maps<a class="footnote-ref" id="fnref:64" href="#fn:64"><sup>64</sup></a></li> <li><a href="/facts/MicroRNA/UjqbYYpe">microRNA</a> in germ layer patterning and eye development<a class="footnote-ref" id="fnref:65" href="#fn:65"><sup>65</sup></a><a class="footnote-ref" id="fnref:66" href="#fn:66"><sup>66</sup></a></li> <li>Link between <a href="/facts/Wnt_signaling/7wxpKrjy">Wnt signaling</a> and <a href="/facts/Telomerase/tUtWedEg">telomerase</a><a class="footnote-ref" id="fnref:67" href="#fn:67"><sup>67</sup></a></li> <li>Development of the <a href="/facts/Vasculature/WXwudzzc">vasculature</a><a class="footnote-ref" id="fnref:68" href="#fn:68"><sup>68</sup></a></li> <li>Gut morphogenesis<a class="footnote-ref" id="fnref:69" href="#fn:69"><sup>69</sup></a></li> <li>Contact inhibition and <a href="/facts/Neural_crest/SgvAz0Ww">neural crest</a> cell migration<a class="footnote-ref" id="fnref:70" href="#fn:70"><sup>70</sup></a> and the generation of neural crest from pluripotent blastula cells<a class="footnote-ref" id="fnref:71" href="#fn:71"><sup>71</sup></a></li> <li>Developmental fate - Role of <i><a href="/facts/Notch_signaling_pathway/5sVkTc0A">Notch</a></i>: Dorsky et al 1995 elucidated a pattern of expression followed by downregulation<a class="footnote-ref" id="fnref:72" href="#fn:72"><sup>72</sup></a></li></ol> <p><a href="/facts/DNA_replication/wrU6RuR3">DNA replication</a>: <i>Xenopus</i> cell-free extracts also support the synchronous assembly and the activation of origins of DNA replication. They have been instrumental in characterizing the biochemical function of the prereplicative complex, including MCM proteins.<a class="footnote-ref" id="fnref:73" href="#fn:73"><sup>73</sup></a><a class="footnote-ref" id="fnref:74" href="#fn:74"><sup>74</sup></a> </p><p><a href="/facts/DNA_damage/hsURuYYq">DNA damage</a> response: Cell-free extracts have been instrumental to unravel the signaling pathways activated in response to DNA double-strand breaks (ATM), replication fork stalling (ATR) or DNA interstrand crosslinks (FA proteins and ATR). Notably, several mechanisms and components of these signal transduction pathways were first identified in <i>Xenopus</i>.<a class="footnote-ref" id="fnref:75" href="#fn:75"><sup>75</sup></a><a class="footnote-ref" id="fnref:76" href="#fn:76"><sup>76</sup></a><a class="footnote-ref" id="fnref:77" href="#fn:77"><sup>77</sup></a> </p><p><a href="/facts/Apoptosis/8dVzSm4y">Apoptosis</a>: <i>Xenopus</i> oocytes provide a tractable model for biochemical studies of apoptosis. Recently, oocytes were used recently to study the biochemical mechanisms of caspase-2 activation; importantly, this mechanism turns out to be conserved in mammals.<a class="footnote-ref" id="fnref:78" href="#fn:78"><sup>78</sup></a> </p><p><a href="/facts/Regenerative_medicine/RplB5P22">Regenerative medicine</a>: In recent years, tremendous interest in developmental biology has been stoked by the promise of regenerative medicine. <i>Xenopus</i> has played a role here, as well. For example, expression of seven transcription factors in pluripotent <i>Xenopus</i> cells rendered those cells able to develop into functional eyes when implanted into <i>Xenopus</i> embryos, providing potential insights into the repair of retinal degeneration or damage.<a class="footnote-ref" id="fnref:79" href="#fn:79"><sup>79</sup></a> In a vastly different study, <i>Xenopus</i> embryos was used to study the effects of tissue tension on morphogenesis,<a class="footnote-ref" id="fnref:80" href="#fn:80"><sup>80</sup></a> an issue that will be critical for <i>in vitro</i> tissue engineering. <i>Xenopus</i> species are important model organisms for the study of spinal cord regeneration, because while capable of regeneration in their larval stages, <i>Xenopus</i> lose this capacity in early metamorphosis.<a class="footnote-ref" id="fnref:81" href="#fn:81"><sup>81</sup></a> </p><p><a href="/facts/Physiology/fh25y2pQ">Physiology</a>: The directional beating of multiciliated cells is essential to development and homeostasis in the central nervous system, the airway, and the oviduct. The multiciliated cells of the <i>Xenopus</i> epidermis have recently been developed as the first <i>in vivo</i> test-bed for live-cell studies of such ciliated tissues, and these studies have provided important insights into the biomechanical and molecular control of directional beating.<a class="footnote-ref" id="fnref:82" href="#fn:82"><sup>82</sup></a><a class="footnote-ref" id="fnref:83" href="#fn:83"><sup>83</sup></a> </p><p><a href="/facts/Actin/Hu3qIUL9">Actin</a>: Another result from cell-free <i>Xenopus</i> oocyte extracts has been improved understanding of actin.<a class="footnote-ref" id="fnref:84" href="#fn:84"><sup>84</sup></a> </p> <h3>Small molecule screens to develop novel therapies</h3> <p>Because huge amounts of material are easily obtained, all modalities of <i>Xenopus</i> research are now being used for small-molecule based screens. </p><p><a href="/facts/Chemical_genetics/kUndhl4x">Chemical genetics</a> of vascular growth in <i>Xenopus</i> tadpoles: Given the important role of neovascularization in cancer progression, <i>Xenopus</i> embryos were recently used to identify new small molecules inhibitors of blood vessel growth. Notably, compounds identified in <i>Xenopus</i> were effective in mice.<a class="footnote-ref" id="fnref:85" href="#fn:85"><sup>85</sup></a><a class="footnote-ref" id="fnref:86" href="#fn:86"><sup>86</sup></a> Notably, frog embryos figured prominently in a study that used evolutionary principles to identify a novel vascular disrupting agent that may have chemotherapeutic potential.<a class="footnote-ref" id="fnref:87" href="#fn:87"><sup>87</sup></a> That work was featured in the New York Times Science Times<a class="footnote-ref" id="fnref:88" href="#fn:88"><sup>88</sup></a> </p><p><i>In vivo</i> testing of potential <a href="/facts/Endocrine_disruptors/Yk2hfnTj">endocrine disruptors</a> in transgenic <i>Xenopus</i> embryos; A high-throughput assay for thyroid disruption has recently been developed using transgenic <i>Xenopus</i> embryos.<a class="footnote-ref" id="fnref:89" href="#fn:89"><sup>89</sup></a> </p><p>Small molecule screens in <i>Xenopus</i> egg extracts: Egg extracts provide ready analysis of molecular biological processes and can rapidly screened. This approach was used to identify novel inhibitors of proteasome-mediated protein degradation and DNA repair enzymes.<a class="footnote-ref" id="fnref:90" href="#fn:90"><sup>90</sup></a><a class="footnote-ref" id="fnref:91" href="#fn:91"><sup>91</sup></a> </p> <h3>Genetic studies</h3> <p>While <i>Xenopus laevis</i> is the most commonly used species for <a href="/facts/Developmental_biology/9dLJhCCv">developmental biology</a> studies, genetic studies, especially forward genetic studies, can be complicated by their <a href="/facts/Ploidy/U8zl4AQe">pseudotetraploid</a> <a href="/facts/Genome/tjhWET4V">genome</a>. <i><a href="/facts/Xenopus_tropicalis/uoS2ALeT">Xenopus tropicalis</a></i> provides a simpler model for genetic studies, having a <a href="/facts/Ploidy/U8zl4AQe">diploid</a> genome. </p> <h3>Gene expression knockdown techniques</h3> <p>The expression of genes can be reduced by a variety of means, for example by using antisense oligonucleotides targeting specific mRNA molecules. DNA oligonucleotides complementary to specific mRNA molecules are often chemically modified to improve their stability <i>in vivo</i>. The chemical modifications used for this purpose include phosphorothioate, 2'-O-methyl, morpholino, MEA phosphoramidate and DEED phosphoramidate.<a class="footnote-ref" id="fnref:92" href="#fn:92"><sup>92</sup></a> </p> <h4>Morpholino oligonucleotides</h4> <p class="note">Main article: <a href="/facts/Morpholino/EsU9Heor">Morpholino</a></p> <p>Morpholino oligos are used in both <i>X. laevis</i> and <i>X. tropicalis</i> to probe the function of a protein by observing the results of eliminating the protein's activity.<a class="footnote-ref" id="fnref:93" href="#fn:93"><sup>93</sup></a><a class="footnote-ref" id="fnref:94" href="#fn:94"><sup>94</sup></a> For example, a set of <i>X. tropicalis</i> genes has been screened in this fashion.<a class="footnote-ref" id="fnref:95" href="#fn:95"><sup>95</sup></a> </p><p>Morpholino oligos (MOs) are short, antisense oligos made of modified nucleotides. MOs can knock down gene expression by inhibiting mRNA translation, blocking RNA splicing, or inhibiting miRNA activity and maturation. MOs have proven to be effective knockdown tools in developmental biology experiments and RNA-blocking reagents for cells in culture. MOs do not degrade their RNA targets, but instead act via a steric blocking mechanism RNAseH-independent manner. They remain stable in cells and do not induce immune responses. Microinjection of MOs in early <i>Xenopus</i> embryos can suppress gene expression in a targeted manner. </p><p>Like all antisense approaches, different MOs can have different efficacy, and may cause off-target, non-specific effects. Often, several MOs need to be tested to find an effective target sequence. Rigorous controls are used to demonstrate specificity,<a class="footnote-ref" id="fnref:96" href="#fn:96"><sup>96</sup></a> including: </p> <ul><li>Phenocopy of genetic mutation</li> <li>Verification of reduced protein by western or immunostaining</li> <li>mRNA rescue by adding back a mRNA immune to the MO</li> <li>use of 2 different MOs (translation blocking and splice blocking)</li> <li>injection of control MOs</li></ul> <p><a href="/facts/Xenbase/c2EFotmu">Xenbase</a> provides a searchable catalog of over 2000 MOs that have been specifically used in Xenopus<i> research.</i> The data is searchable via sequence, gene symbol and various synonyms (as used in different publications).<a class="footnote-ref" id="fnref:97" href="#fn:97"><sup>97</sup></a> Xenbase maps the MOs to the latest <i>Xenopus</i> genomes in GBrowse, predicts 'off-target' hits, and lists all <i>Xenopus</i> literature in which the morpholino has been published. </p> <h2 id="external-links">External links</h2> <ul><li><a href="http://www.xenbase.org/">Xenbase</a> ~ A <i>Xenopus laevis</i> and <i>tropicalis</i> Web Resource</li></ul> <h2 id="references">References</h2> <ol> <li id="fn:1"><p>"Xenopus". 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Retrieved 2009-10-11. <a href="https://web.archive.org/web/20100626190703/http://www.iacuc.arizona.edu/training/xenopus/intro.html" target="_blank">https://web.archive.org/web/20100626190703/http://www.iacuc.arizona.edu/training/xenopus/intro.html</a> <a href="#fnref:18" class="footnote-back-ref">↩</a></p></li> <li id="fn:19"><p>Wallingford JB, Liu KJ, Zheng Y (March 2010). "Xenopus". Current Biology. 20 (6): R263 – R264. Bibcode:2010CBio...20.R263W. doi:10.1016/j.cub.2010.01.012. PMID 20334828. <a href="https://doi.org/10.1016%2Fj.cub.2010.01.012" target="_blank">https://doi.org/10.1016%2Fj.cub.2010.01.012</a> <a href="#fnref:19" class="footnote-back-ref">↩</a></p></li> <li id="fn:20"><p>Harland RM, Grainger RM (December 2011). "Xenopus research: metamorphosed by genetics and genomics". Trends in Genetics. 27 (12): 507–515. doi:10.1016/j.tig.2011.08.003. PMC 3601910. 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