نشكر السيدة فان شين عن دعمها للتربية الزرد. ويؤيد ذلك بالتمويل هو جين بينغ إلى الدكتور (الأكاديمية الصينية للعلوم ، &quot;باي هوا رن جى&quot; ، NSFC 30870833 والبرنامج الوطني للعلوم الأساسية للصين ، 2009CB941302). وأجريت التجارب على الحيوانات فقط وفقا للمبادئ التوجيهية واللوائح التي وضعتها جامعة العلوم والتكنولوجيا في الصين (USTC) مركز الموارد الحيوانية وجامعة ولجنة رعاية الحيوان الاستخدام.

الجزء الأول : بناء جهاز OKR وترد التفاصيل في تظاهرة الفيديو. الجزء الثاني : OKR من اسماك الزرد الكبار إذا كان المختبر الخاص شيدت جهاز OKR ، مفتاح أخلاقي الزرد OKR هو اجراء السمك. في هذا الجزء ، وسوف نظهر لكم خطوة خطوة. لدينا جهاز يؤلف الأجزاء التالية مشابهة للآخرين المذكورة. غرفة الأسماك التعميم هو 7.0 سم وقطرها الخارجي ، 6.5 سم في القطر الداخلي و 7.0 سم في ارتفاع. أسطوانة حول الغرفة الأسماك 8.5 سم وقطرها من 7.5 سم في القطر الداخلي و 7.0 سم في ارتفاع. يمكن أن تدوير في اتجاه عقارب الساعة وعقارب الساعة مع سرعة في الفترة من 20 ~ 70 دقيقة لكل تناوب (دورة في الدقيقة). يتم رسمها أحد عشر دورات من خطوط سوداء وبيضاء على ورقة البحث عن المفقودين التي انضمت على السطح الخارجي للأسطوانة. ويتألف النظام من أنبوبين ضوء ضوء دائرة قطرها 21 سم. <img src="/files/ftp_upload/1742/1742fig1.jpg" alt="الشكل 1" /> الشكل 1. نموذج من الإسفنج ، وجرف المحرز في هذا الوسط هو التأكد من أنه لا مجال المرئي تأويه. <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> اسفنجة كما هو مبين في Fig.1 مكونة من جزأين. في الجزء الأيسر بطول 3 سم * 3 سم x العرض 2 سم ارتفاع. الجزء الصحيح هو طول 3 سم x العرض 3 سم x ارتفاع 3 سم. </li><li style=";text-align:right;direction:rtl"> وضع هذه الاسفنجة في الجزء السفلي من الغرفة الأسماك وتربية صب الماء في عمق حوالي 2 سم. وينبغي أن يكون الدافع وراء فقاعة الهواء التي تخفي في محا. </li><li style=";text-align:right;direction:rtl"> اضافة الى وجود دبوس في الجزء الأمامي من الجزء الأيمن من الاسفنج ، وحوالي 2 ملم وراء الهاوية. </li><li style=";text-align:right;direction:rtl"> تخدير an الزرد الكبار في MS - 222. </li><li style=";text-align:right;direction:rtl"> وضع الزرد على الإسفنج مع ما يصل الظهرية والسماح جانب واحد من الزعنفة الصدرية لها قبل طرف الأول. </li><li style=";text-align:right;direction:rtl"> يتم إدراج دبوس الثاني خلف الزعنفة الصدرية الأخرى. يمكن أن تجنب انكماش الزرد الجسم من خلال التعاون مع طرف الأول (انظر أيضا في الشكل 2). </li><li style=";text-align:right;direction:rtl"> المشبك ذيله مع الشريان المشبك المشبك وإصلاح الشريان في قطعة من المطاط (الصلصال) والتي انضمت في غرفة الأسماك. </li><li style=";text-align:right;direction:rtl"> هي التي زرعت دبوس الثالث والرابع في موقع بالقرب من مسام الجسد المذرقية الأسماك. ويمكن أن يمنع الزرد لموجة ذيله بشكل مكثف. </li><li style=";text-align:right;direction:rtl"> ويقع مقر دبوس الخامسة بين الأول والثالث ودبوس دبوس ثم السادس على الجانب الآخر منه. يمكن أن تمنع من الزرد تهز جسمها. </li><li style=";text-align:right;direction:rtl"> يتم إدراج دبوس والسابعة والثامنة في مواقع بالقرب من الخياشيم للحفاظ على اتجاه الرأس. </li><li style=";text-align:right;direction:rtl"> صب الماء في غرفة تربية الأسماك. </li><li style=";text-align:right;direction:rtl"> بعد الزرد يستيقظ ، والسماح لها التكيف لمدة 5 دقائق 10 ~. </li><li style=";text-align:right;direction:rtl"> التبديل على ضوء هذا الجهاز والسماح الزرد تكييف هذه الإضاءة لمدة 2 دقيقة. </li><li style=";text-align:right;direction:rtl"> التبديل على المحرك إلى محرك صريف الزرد والسماح للتكيف لمدة 1 دقيقة. </li><li style=";text-align:right;direction:rtl"> بدوره على الكاميرا وتسجيل حركة العينين. </li><li style=";text-align:right;direction:rtl"> تحليل زوايا العين (6) وأرقام رمش على الكمبيوتر الشخصية (هو مبين مثال ممثل العين زوايا التحليل في Fig.2). </li></ol><img src="/files/ftp_upload/1742/1742fig2.jpg" alt="الشكل 2" /> الشكل 2. زاوية العين وبين المحور محور الجسم. حددنا أ) عندما يكون اتجاه حزيز والأنف إلى موقتا ، في زاوية قبل هيئة الأسماك زاوية سلبية وزاوية في جسم السمكة هو زاوية إيجابية ، والعكس بالعكس (لاستعراض موجز انظر أيضا المرجع. 6). الأرقام في هذا الرقم يمثل تسلسل من الدبابيس. ب) تحليل المثال OKR من الأسماك في المجموعة العادية. ونقلت فيلم ثانية واحدة لسلسلة الإطارات وقياس الزوايا عين كل إطار مع صورة للمحترفين البرمجيات زائد. كل نقطة في هذا الرقم يمثل كل إطار علينا قياسه. ملاحظات : <ol class="lalpha" style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> وتستخدم فقط كل المسامير من الزرد لمنع اهتزاز جسمها أيضا سوف تكون ضيقة تضر الأسماك. </li><li style=";text-align:right;direction:rtl"> يمكن المشبك الشريان الضرر الذيل ومنطقتها الاتصال صغيرة. مرة واحدة في الذيل هو الحرة ، فمن الصعب جدا لإصلاح هذه الأسماك. لف ضمادة حول الذيل ويوصى في بعض الشرط. </li><li style=";text-align:right;direction:rtl"> ينبغي للدبوس والسابعة والثامنة التي زرعت في موقع بالقرب من الخياشيم لا تكون ملجأ من أبصارهم من صريف. </li></ol> الجزء الثالث. OKR من اسماك الزرد اليرقات 1. Methylcellulose يمكن أن يجمد اليرقات الزرد في حل methylcellulose 6 ٪ في حين تبقي على قيد الحياة لفترة طويلة. يعد حل methylcellulose على النحو التالي. <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> يغلي 200 مل DDH 2 O في المايكرويف حوالي 3 دقائق على مستوى عال. </li><li style=";text-align:right;direction:rtl"> نقل الماء الساخن لموقد اثارة وتحريك بقوة. </li><li style=";text-align:right;direction:rtl"> إضافة 12 methylcellulose ز في الماء الساخن تدريجيا. </li><li style=";text-align:right;direction:rtl"> ابقاء التحريك لمدة 3 دقائق بعد methylcellulose جيدا متفرقة. </li><li style=";text-align:right;direction:rtl"> مع حلول تبريد الماء المثلج حتى يصبح واضحا ، ووضع بعد ذلك في 4 درجات مئوية. </li></ol><pالطبقة = &quot;jove_step&quot;&gt; 2. يرقات اسماك الزرد <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> زوجين من الذكور والإناث من الزرد الكبار في خزان التزاوج في الساعة 17:00 بعد الرضاعة. صباح اليوم التالي نقلها إلى خزان التزاوج الطازجة وجمع الأجنة بعد 1 ساعة. </li><li style=";text-align:right;direction:rtl"> والحفاظ على البيض في المتوسط ​​28.5 في جنين ± 0.5 درجة مئوية مع حاضنة النور : دورة المظلمة 14:10. </li><li style=";text-align:right;direction:rtl"> فقس البيض وسيتم في 48 من أصل إخصاب آخر ساعة (HPF) وسيتم اختبار OKR HPF في 72 أو في وقت لاحق. في هذا الفيديو ، ويتم في 5 larvaes DPF. </li></ol> 3. إجراءات OKR <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> وضع الجهاز تحت المجسام مزودة كاميرا CCD والتبديل على ضوء هذا الجهاز. </li><li style=";text-align:right;direction:rtl"> إضافة 20 مل methycellulose 6 ٪ في طبق بتري 55 ملم. </li><li style=";text-align:right;direction:rtl"> مكان larvaes عدة في صف واحد في وسط هذا الطبق. </li><li style=";text-align:right;direction:rtl"> وضع فقاعة الهواء حول حجم 1 ميكرولتر في مجال الكاميرا ، ويمكن أن يكون بمثابة مرآة تعكس اتجاه صريف. </li><li style=";text-align:right;direction:rtl"> التبديل على السيارات وتسجيل حركة أعينهم. </li></ol> الجزء الرابع. ريال عماني للاسماك الزرد الكبار ويمكن أيضا الكبار الزرد ريال عماني تجري مع هذا الجهاز ، مجرد مكان العمود في غرفة الأسماك لمنع السباحة الأسماك عبر مركز (أظهر في Fig.3a والسرعة الدورية هي 36 دورة في الدقيقة ، أسود وأبيض دورات 11). <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> وضع الأسماك في هذه القاعة الأسماك. </li><li style=";text-align:right;direction:rtl"> يقف عمود بقطر 2 سم في وسط هذه القاعة الأسماك. </li><li style=";text-align:right;direction:rtl"> التكيف لدقيقة واحدة في كل من لا يزال وصريف صريف التناوب. </li><li style=";text-align:right;direction:rtl"> سجل حركة الزرد. </li><li style=";text-align:right;direction:rtl"> تحليل معدل صدفة من الوقت على جهاز الكمبيوتر الشخصي (يظهر على سبيل المثال في Fig.3b ، تناوب السرعة هي 36 دورة في الدقيقة ، أسود وأبيض دورة 11) </li></ol><img src="/files/ftp_upload/1742/1742fig3.jpg" alt="الشكل 3" /> الشكل 3. ريال عماني للاسماك الزرد الكبار. (أ) وضعت عمود البلاستيكية البيضاء في وسط الغرفة الأسماك لمنع السباحة الأسماك عبرها. (ب) ويبلغ معدل تزامن الزرد الكبار التالية صريف. وقد عرفت نسبة مصادفة حيث أن نسبة من الوقت صريف التالية لتسجيل الوقت الإجمالي. القيمة 50 ٪ يشير إلى أن الأسماك هي السباحة بشكل عشوائي في حين يشير إلى 100 ٪ صريف التالية السمك بشكل جيد جدا. وسحق كل من الأعصاب البصرية مع ملقط المجوهرات حوالي 10 ثانية. يبدو أن السلوك ريال عماني كما السباحة العشوائية بعد سحق.

<ol>
	<li>Beck, J., Gilland, E., Tank, D., Baker, R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Quantifying+the+Ontogeny+of+Optokinetic+and+Vestibuloocular+Behaviors+in+Zebrafish+Medaka,+and+Goldfish.">Quantifying the Ontogeny of Optokinetic and Vestibuloocular Behaviors in Zebrafish Medaka, and Goldfish.</a> J Neurophysiol. 92, 3546-3561 (2004).</li><li>Brockerhoff, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Measuring+the+optokinetic+response+of+zebrafish+larvae.">Measuring the optokinetic response of zebrafish larvae.</a> Nature Protocols. 1, 2448-2451 (2006).</li><li>Emran, F. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=OFF+ganglion+cells+cannot+drive+the+optokinetic+reflex+in+zebrafish.">OFF ganglion cells cannot drive the optokinetic reflex in zebrafish.</a> Proc Natl Acad Sci U S A. 104, 19126-19131 (2007).</li><li>Rinner, O., Rick, J., Neuhauss, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Contrast+Sensitivity,+Spatial+and+Temporal+Tuning+of+the+Larval+Zebrafish+Optokinetic+Response.">Contrast Sensitivity, Spatial and Temporal Tuning of the Larval Zebrafish Optokinetic Response.</a> Investigative Ophthalmology and Visual Science. 46, 137-142 (2005).</li><li>Roeser, T., Baier, H. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Visuomotor+Behaviors+in+Larval+Zebrafish+after+GFP-Guided+Laser+Ablation+of+the+Optic+Tectum.">Visuomotor Behaviors in Larval Zebrafish after GFP-Guided Laser Ablation of the Optic Tectum.</a> The Journal of Neuroscience. 23, 3726-3734 (2003).</li><li>Easter, S., Nicola, G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+Development+of+Vision+in+the+Zebrafish+(Danio+rerio).">The Development of Vision in the Zebrafish (Danio rerio).</a> Developmental Biology. 180, 646-663 (1996).</li><li>Maaswinkel, H., Li, L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Spatio-temporal+frequency+characteristics+of+the+optomotor+response+in+zebrafish.">Spatio-temporal frequency characteristics of the optomotor response in zebrafish.</a> Vision Research. 43, 21-30 (2003).</li></ol>

وفقا للتعريف OKR ، بل هو ظاهرة أن الحيوانات تتحرك عيونهم لمتابعة الدورية صريف عفويا. إذا كان قد تم إجراء هذا السلوك لفترة طويلة (على سبيل المثال أكثر من 6 ساعات) ، قد يكون متعبا في عضلات العين وسيتم OKR الموهن. وقد وصفت البالغين الزرد ر...

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<td>Methylcellulose</td>
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using the optokinetic response to study visual function of zebrafish

استجابة Optokinetic (OKR) هو السلوك الذي يهتز حيوان عينيه عن اتباع صريف تدور حوله. وقد استخدم على نطاق واسع لتقييم الوظائف البصرية اليرقات الزرد 1-5. ومع ذلك ، فإن بروتوكول قياسي للأسماك اليرقات ليس بعد تطبيق بسهولة في zabrafish الكبار. هنا ، نحن نقدم كيفية قياس OKR من الزرد الكبار مع جهاز عادتنا بسيطة بنيت باستخدام بروتوكول الجديدة التي أنشئت في المختبر. ويوضح لنا كل من أجهزة وخطوة بخطوة الداخلي OKR في الزرد الكبار في هذا الفيديو. بالإضافة إلى ذلك ، وكما أظهرت قياسات OKR اليرقات ، فضلا عن الاستجابة optomotor (ريال عماني) اختبار الزرد الكبار ، في هذا الفيديو. قد يكون هذا الفحص OKR من الزرد الكبار في تجربتنا تستمر لمدة تصل إلى 4 ساعات. وسوف تطبق هذه التجربة في OKR الأسماك البالغة لتحقيق الاستفادة بشكل أكثر كفاءة وظيفة البصرية عندما يتم التلاعب رؤية الأسماك نظام أخلاقي. سو تشي ساهمت زو ويين وو بالتساوي على هذه الورقة.

Watch this Scientific Journal Video about Using the optokinetic response to study visual function of zebrafish at JoVE.com

Using the optokinetic response to study visual function of zebrafish

وكان رد Optokinetic المستخدمة على نطاق واسع لتقييم الوظائف البصرية الزرد اليرقات. ومع ذلك ، فإن بروتوكول قياسي للأسماك اليرقات ليست سهلة التطبيق حتى الآن في البالغين<sup&gt; 1-5</sup&gt;. هنا ، نحن نقدم كيفية قياس OKR من الزرد الكبار باستخدام بروتوكول الجديدة التي أنشئت في المختبر.

باستخدام optokinetic استجابة لدراسة وظيفة البصرية من الزرد

Optokinetic response (OKR) is a behavior that an animal vibrates its eyes to follow a rotating grating around it. It has been widely used to assess the ...

using-the-optokinetic-response-to-study-visual-function-of-zebrafish

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Biology

18.2K Views.  University of Science and Technology of China (USTC). وكان رد Optokinetic المستخدمة على نطاق واسع لتقييم الوظائف البصرية الزرد اليرقات. ومع ذلك ، فإن بروتوكول قياسي للأسماك اليرقات ليست سهلة التطبيق حتى الآن في البالغين 1-5. هنا ، نحن نقدم كيفية قياس OKR من الزرد الكبار باستخدام بروتوكول الجديدة التي أنشئت في المخ...

Video: Using the optokinetic response to study visual function of zebrafish

Testing Visual Sensitivity to the Speed and Direction of Motion in Lizards

Testing visual sensitivity in any species provides basic information regarding behaviour, evolution, and ecology. However, testing specific features of the visual system provide more empirical evidence for functional applications. Investigation into the sensory system provides information about the sensory capacity, learning and memory ability, and establishes known baseline behaviour in which to gauge deviations (Burghardt, 1977). However, unlike mammalian or avian systems, testing for learning and memory in a reptile species is difficult. Furthermore, using an operant paradigm as a psychophysical measure of sensory ability is likewise as difficult. Historically, reptilian species have responded poorly to conditioning trials because of issues related to motivation, physiology, metabolism, and basic biological characteristics. Here, I demonstrate an operant paradigm used a novel model lizard species, the Jacky dragon (Amphibolurus muricatus) and describe how to test peripheral sensitivity to salient speed and motion characteristics. This method uses an innovative approach to assessing learning and sensory capacity in lizards. I employ the use of random-dot kinematograms (RDKs) to measure sensitivity to speed, and manipulate the level of signal strength by changing the proportion of dots moving in a coherent direction. RDKs do not represent a biologically meaningful stimulus, engages the visual system, and is a classic psychophysical tool used to measure sensitivity in humans and other animals. Here, RDKs are displayed to lizards using three video playback systems. Lizards are to select the direction (left or right) in which they perceive dots to be moving. Selection of the appropriate direction is reinforced by biologically important prey stimuli, simulated by computer-animated invertebrates.

Testing visual sensitivity in lizards using an operant conditioning paradigm that employs video playback of random-dot kinematograms and computer-generated invertebrates.

اختبار الحساسية البصرية للسرعة واتجاه الحركة في السحالي

Testing visual sensitivity in any species provides basic information regarding behaviour, evolution, and ecology. However, testing specific features of ...

Computer-Generated Animal Model Stimuli

Communication between animals is diverse and complex. Animals may communicate using auditory, seismic, chemosensory, electrical, or visual signals. In particular, understanding the constraints on visual signal design for communication has been of great interest. Traditional methods for investigating animal interactions have used basic observational techniques, staged encounters, or physical manipulation of morphology. Less intrusive methods have tried to simulate conspecifics using crude playback tools, such as mirrors, still images, or models. As technology has become more advanced, video playback has emerged as another tool in which to examine visual communication (Rosenthal, 2000). However, to move one step further, the application of computer-animation now allows researchers to specifically isolate critical components necessary to elicit social responses from conspecifics, and manipulate these features to control interactions. Here, I provide detail on how to create an animation using the Jacky dragon as a model, but this process may be adaptable for other species. In building the animation, I elected to use Lightwave  3D to alter object morphology, add texture, install bones, and provide comparable weight shading that prevents exaggerated movement. The animation is then matched to select motor patterns to replicate critical movement features. Finally, the sequence must rendered into an individual clip for presentation. Although there are other adaptable techniques, this particular method had been demonstrated to be effective in eliciting both conspicuous and social responses in staged interactions.

Computer-generated stimuli using the Jacky dragon as a model.

الحاسوب خلق المحفزات الحيوان النموذجي

Communication between animals is diverse and complex. Animals may communicate using auditory, seismic, chemosensory, electrical, or visual signals. In ...

Microinjection of Zebrafish Embryos to Analyze Gene Function

One of the advantages of studying zebrafish is the ease and speed of manipulating protein levels in the embryo.  Morpholinos, which are synthetic oligonucleotides with antisense complementarity to target RNAs, can be added to the embryo to reduce the expression of a particular gene product.  Conversely, processed mRNA can be added to the embryo to increase levels of a gene product.  The vehicle for adding either mRNA or morpholino to an embryo is microinjection.  Microinjection is efficient and rapid, allowing for the injection of hundreds of embryos per hour.  This video shows all the steps involved in microinjection.  Briefly, eggs are collected immediately after being laid and lined up against a microscope slide in a Petri dish.  Next, a fine-tipped needle loaded with injection material is connected to a microinjector and an air source, and the microinjector controls are adjusted to produce a desirable injection volume.  Finally, the needle is plunged into the embryo's yolk and the morpholino or mRNA is expelled.

This video shows how morpholino or mRNA can be injected into zebrafish embryos at the one-cell stage to decrease or increase the level of specific gene products during subsequent development.

Microinjection الجنين اسماك الزرد إلى تحليل وظائف الجينات

One of the advantages of studying zebrafish is the ease and speed of manipulating protein levels in the embryo.  Morpholinos, which are synthetic ...

Methods for the Study of the Zebrafish Maxillary Barbel

Barbels are skin sensory appendages found in fishes, reptiles and amphibians. The zebrafish, Danio rerio, develops two pairs of barbels- a short nasal pair and a longer maxillary pair. Barbel tissue contains cells of ectodermal, mesodermal and neural crest origin, including skin cells, glands, taste buds, melanocytes, circulatory vessels and sensory nerves. Unlike most adult tissue, the maxillary barbel is optically clear, allowing us to visualize the development and maintenance of these tissue types throughout the life cycle. 
This video shows early development of the maxillary barbel (beginning approximately one month post-fertilization) and demonstrates a surgical protocol to induce regeneration in the adult appendage (&gt;3 months post-fertilization). Briefly, the left maxillary barbel of an anesthetized fish is elevated with sterile forceps just distal to the caudal edge of the maxilla. A fine, sterile spring scissors is positioned against the forceps to cut the barbel shaft at this level, establishing an anatomical landmark for the amputation plane. Regenerative growth can be measured with respect to this plane, and in comparison to the contralateral barbel. Barbel tissue regenerates rapidly, reaching maximal regrowth within 2 weeks of injury.
Techniques for analyzing the regenerated barbel include dissecting and embedding matched pairs of barbels (regenerate and control) in the wells of a standard DNA electrophoresis gel. Embedded specimens are conveniently photographed under a stereomicroscope for gross morphology and morphometry, and can be stored for weeks prior to downstream applications such as paraffin histology, cryosectioning, and/or whole mount immunohistochemistry. These methods establish the maxillary barbel as a novel in vivo tissue system for studying the regenerative capacity of multiple cell types within the genetic context of zebrafish.

The zebrafish maxillary barbel is an integumentary sense organ containing ectodermal, mesodermal and neural crest derivatives. Importantly, the adult barbel can regenerate after proximal amputation. This video introduces maxillary barbel development and demonstrates a surgical protocol to induce regeneration, followed by collection, embedding and downstream imaging of barbel specimens.

طرق لدراسة بربل الفكين اسماك الزرد

Barbels are skin sensory appendages found in fishes, reptiles and amphibians.  The zebrafish, Danio rerio, develops two pairs of barbels- a short nasal ...

Hi-C: A Method to Study the Three-dimensional Architecture of Genomes.

The three-dimensional folding of chromosomes compartmentalizes the genome and and can bring distant functional elements, such as promoters and enhancers, into close spatial proximity 2-6. Deciphering the relationship between chromosome organization and genome activity will aid in understanding genomic processes, like transcription and replication. However, little is known about how chromosomes fold. Microscopy is unable to distinguish large numbers of loci simultaneously or at high resolution. To date, the detection of chromosomal interactions using chromosome conformation capture (3C) and its subsequent adaptations required the choice of a set of target loci, making genome-wide studies impossible 7-10.
We developed Hi-C, an extension of 3C that is capable of identifying long range interactions in an unbiased, genome-wide fashion. In Hi-C, cells are fixed with formaldehyde, causing interacting loci to be bound to one another by means of covalent DNA-protein cross-links. When the DNA is subsequently fragmented with a restriction enzyme, these loci remain linked. A biotinylated residue is incorporated as the 5' overhangs are filled in. Next, blunt-end ligation is performed under dilute conditions that favor ligation events between cross-linked DNA fragments. This results in a genome-wide library of ligation products, corresponding to pairs of fragments that were originally in close proximity to each other in the nucleus. Each ligation product is marked with biotin at the site of the junction. The library is sheared, and the junctions are pulled-down with streptavidin beads. The purified junctions can subsequently be analyzed using a high-throughput sequencer, resulting in a catalog of interacting fragments.
Direct analysis of the resulting contact matrix reveals numerous features of genomic organization, such as the presence of chromosome territories and the preferential association of small gene-rich chromosomes. Correlation analysis can be applied to the contact matrix, demonstrating that the human genome is segregated into two compartments: a less densely packed compartment containing open, accessible, and active chromatin and a more dense compartment containing closed, inaccessible, and inactive chromatin regions. Finally, ensemble analysis of the contact matrix, coupled with theoretical derivations and computational simulations, revealed that at the megabase scale Hi-C reveals features consistent with a fractal globule conformation.

The Hi-C method allows unbiased, genome-wide identification of chromatin interactions (1). Hi-C couples proximity ligation and massively parallel sequencing. The resulting data can be used to study genomic architecture at multiple scales: initial results identified features such as chromosome territories, segregation of open and closed chromatin, and chromatin structure at the megabase scale.

مرحبا - C : طريقة لدراسة الهندسة المعمارية ثلاثي الأبعاد للخريطة جينوم.

The three-dimensional folding of chromosomes compartmentalizes the genome and and can bring distant functional elements, such as promoters and enhancers, ...

Quantification of &gamma;H2AX Foci in Response to Ionising Radiation

DNA double-strand breaks (DSBs), which are induced by either endogenous metabolic processes or by exogenous sources, are one of the most critical DNA lesions with respect to survival and preservation of genomic integrity. An early response to the induction of DSBs is phosphorylation of the H2A histone variant, H2AX, at the serine-139 residue, in the highly conserved C-terminal SQEY motif, forming &gamma;H2AX1. Following induction of DSBs, H2AX is rapidly phosphorylated by the phosphatidyl-inosito 3-kinase (PIKK) family of proteins, ataxia telangiectasia mutated (ATM), DNA-protein kinase catalytic subunit and ATM and RAD3-related (ATR)2. Typically, only a few base-pairs (bp) are implicated in a DSB, however, there is significant signal amplification, given the importance of chromatin modifications in DNA damage signalling and repair. Phosphorylation of H2AX mediated predominantly by ATM spreads to adjacent areas of chromatin, affecting approximately 0.03% of total cellular H2AX per DSB2,3. This corresponds to phosphorylation of approximately 2000 H2AX molecules spanning ~2 Mbp regions of chromatin surrounding the site of the DSB and results in the formation of discrete &gamma;H2AX foci which can be easily visualized and quantitated by immunofluorescence microscopy2. The loss of &gamma;H2AX at DSB reflects repair, however, there is some controversy as to what defines complete repair of DSBs; it has been proposed that rejoining of both strands of DNA is adequate however, it has also been suggested that re-instatement of the original chromatin state of compaction is necessary4-8. The disappearence of &gamma;H2AX involves at least in part, dephosphorylation by phosphatases, phosphatase 2A and phosphatase 4C5,6. Further, removal of &gamma;H2AX by redistribution involving histone exchange with H2A.Z has been implicated7,8. Importantly, the quantitative analysis of &gamma;H2AX foci has led to a wide range of applications in medical and nuclear research. Here, we demonstrate the most commonly used immunofluorescence method for evaluation of initial DNA damage by detection and quantitation of &gamma;H2AX foci in &gamma;-irradiated adherent human keratinocytes9.

Quantification of &amp;#947;H2AX Foci in Response to Ionising Radiation

Quantification of DNA double-strand streaks using &gamma;H2AX formation as a molecular marker has become an invaluable tool in radiation biology. Here we demonstrate the use of an immunofluorescence assay for quantification of &gamma;H2AX foci after exposure of cells to radiation.

الكمي بؤر γH2AX في الاستجابة للإشعاع المؤين

DNA double-strand breaks (DSBs), which are induced by either endogenous metabolic processes or by exogenous sources, are one of the most critical DNA ...

Laser Ablation of the Zebrafish Pronephros to Study Renal Epithelial Regeneration

Acute kidney injury (AKI) is characterized by high mortality rates from deterioration of renal function over a period of hours or days that culminates in renal failure1. AKI can be caused by a number of factors including ischemia, drug-based toxicity, or obstructive injury1. This results in an inability to maintain fluid and electrolyte homeostasis. While AKI has been observed for decades, effective clinical therapies have yet to be developed. Intriguingly, some patients with AKI recover renal functions over time, a mysterious phenomenon that has been only rudimentally characterized1,2. Research using mammalian models of AKI has shown that ischemic or nephrotoxin-injured kidneys experience epithelial cell death in nephron tubules1,2, the functional units of the kidney that are made up of a series of specialized regions (segments) of epithelial cell types3. Within nephrons, epithelial cell death is highest in proximal tubule cells. There is evidence that suggests cell destruction is followed by dedifferentiation, proliferation, and migration of surrounding epithelial cells, which can regenerate the nephron entirely1,2. However, there are many unanswered questions about the mechanisms of renal epithelial regeneration, ranging from the signals that modulate these events to reasons for the wide variation of abilities among humans to regenerate injured kidneys.
The larval zebrafish provides an excellent model to study kidney epithelial regeneration as its pronephric kidney is comprised of nephrons that are conserved with higher vertebrates including mammals4,5. The nephrons of zebrafish larvae can be visualized with fluorescence techniques because of the relative transparency of the young zebrafish6. This provides a unique opportunity to image cell and molecular changes in real-time, in contrast to mammalian models where nephrons are inaccessible because the kidneys are structurally complex systems internalized within the animal. Recent studies have employed the aminoglycoside gentamicin as a toxic causative agent for study of AKI and subsequent renal failure: gentamicin and other antibiotics have been shown to cause AKI in humans, and researchers have formulated methods to use this agent to trigger kidney damage in zebrafish7,8. However, the effects of aminoglycoside toxicity in zebrafish larvae are catastrophic and lethal, which presents a difficulty when studying epithelial regeneration and function over time. Our method presents the use of targeted cell ablation as a novel tool for the study of epithelial injury in zebrafish. Laser ablation gives researchers the ability to induce cell death in a limited population of cells. Varying areas of cells can be targeted based on morphological location, function, or even expression of a particular cellular phenotype. Thus, laser ablation will increase the specificity of what researchers can study, and can be a powerful new approach to shed light on the mechanisms of renal epithelial regeneration. This protocol can be broadly applied to target cell populations in other organs in the zebrafish embryo to study injury and regeneration in any number of contexts of interest.

Acute kidney injury (AKI) in humans is a common clinical problem caused by damage to the epithelial cells that comprise kidney nephrons, and AKI is associated with high mortality rates of 50-70%1. Following epithelial cell destruction, nephrons have a limited ability to regenerate, though the mechanisms and limitations that guide this phenomenon remain poorly understood. In this video article, we describe our technique for targeted laser ablation of kidney nephron cells in the zebrafish embryo kidney, or pronephros. Our new method can be used to complement nephrotoxicity-induced models of AKI and gain a high-resolution understanding of the cell and molecular alterations that are associated with epithelial regeneration in the kidney nephron.

تذرية الليزر للاسماك الزرد سليفة الكلوة لدراسة التجديد طلائي الكلوي

Acute kidney injury (AKI) is characterized by high mortality rates from deterioration of renal function over a period of hours or days that culminates in ...

Force Measurement During Contraction to Assess Muscle Function in Zebrafish Larvae

Zebrafish larvae provide models of muscle development, muscle disease and muscle-related chemical toxicity, but related studies often lack functional measures of muscle health. In this video article, we demonstrate a method to measure force generation during contraction of zebrafish larval trunk muscle. Force measurements are accomplished by placing an anesthetized larva into a chamber filled with a salt solution. The anterior end of the larva is tied to a force transducer and the posterior end of the larva is tied to a length controller. An isometric twitch contraction is elicited by electric field stimulation and the force response is recorded for analysis. Force generation during contraction provides a measure of overall muscle health and specifically provides a measure of muscle function. Although we describe this technique for use with wild-type larvae, this method can be used with genetically modified larvae or with larvae treated with drugs or toxicants, to characterize muscle disease models and evaluate treatments, or to study muscle development, injury, or chemical toxicity.

Force measurements can be used to demonstrate changes in muscle function due to development, injury, disease, treatment or chemical toxicity. In this video, we demonstrate a method to measure force during a maximal contraction of zebrafish larval trunk muscle.

قياس القوة خلال تقلص العضلات لتقييم وظيفة في يرقات اسماك الزرد

Zebrafish larvae provide models of muscle development, muscle disease and muscle-related chemical toxicity, but related studies often lack functional ...

High Resolution Whole Mount In Situ Hybridization within Zebrafish Embryos to Study Gene Expression and Function

This article focuses on whole-mount in situ hybridization (WISH) of zebrafish embryos. The WISH technology facilitates the assessment of gene expression both in terms of tissue distribution and developmental stage. Protocols are described for the use of WISH of zebrafish embryos using antisense RNA probes labeled with digoxigenin. Probes are generated by incorporating digoxigenin-linked nucleotides through in vitro transcription of gene templates that have been cloned and linearized. The chorions of embryos harvested at defined developmental stages are removed before incubation with specific probes. Following a washing procedure to remove excess probe, embryos are incubated with anti-digoxigenin antibody conjugated with alkaline phosphatase. By employing a chromogenic substrate for alkaline phosphatase, specific gene expression can be assessed. Depending on the level of gene expression the entire procedure can be completed within 2-3 days.

High Resolution Whole Mount In Situ Hybridization within Zebrafish Embryos to Study Gene Expression and Function

The zebrafish, a small tropical fish, has become a popular model for studying gene function during vertebrate development and disease. The temporal and spatial expression of target genes can be determined by in situ hybridization. Our improved protocol allows for the detection of low abundant transcripts with low non-specific background signal.

ارتفاع القرار جبل بأكمله<em&gt; في الموضع</em&gt; التهجين داخل الأجنة الزرد لدراسة التعبير الجيني وظيفة

This article focuses on whole-mount in situ hybridization (WISH) of zebrafish embryos. The WISH technology facilitates the assessment of gene expression ...

Analysis of Nephron Composition and Function in the Adult Zebrafish Kidney

The zebrafish model has emerged as a relevant system to study kidney development, regeneration and disease. Both the embryonic and adult zebrafish kidneys are composed of functional units known as nephrons, which are highly conserved with other vertebrates, including mammals. Research in zebrafish has recently demonstrated that two distinctive phenomena transpire after adult nephrons incur damage: first, there is robust regeneration within existing nephrons that replaces the destroyed tubule epithelial cells; second, entirely new nephrons are produced from renal progenitors in a process known as neonephrogenesis. In contrast, humans and other mammals seem to have only a limited ability for nephron epithelial regeneration. To date, the mechanisms responsible for these kidney regeneration phenomena remain poorly understood. Since adult zebrafish kidneys undergo both nephron epithelial regeneration and neonephrogenesis, they provide an outstanding experimental paradigm to study these events. Further, there is a wide range of genetic and pharmacological tools available in the zebrafish model that can be used to delineate the cellular and molecular mechanisms that regulate renal regeneration. One essential aspect of such research is the evaluation of nephron structure and function. This protocol describes a set of labeling techniques that can be used to gauge renal composition and test nephron functionality in the adult zebrafish kidney. Thus, these methods are widely applicable to the future phenotypic characterization of adult zebrafish kidney injury paradigms, which include but are not limited to, nephrotoxicant exposure regimes or genetic methods of targeted cell death such as the nitroreductase mediated cell ablation technique. Further, these methods could be used to study genetic perturbations in adult kidney formation and could also be applied to assess renal status during chronic disease modeling.

The zebrafish adult kidney is an excellent system for renal regeneration and disease studies. An essential aspect of such research is the assessment of nephron structure and function. This protocol describes several methodologies that can be implemented to assess nephron tubule composition and to evaluate renal reabsorption.

تحليل التركيب كليون وظيفة في الكلى اسماك الزرد الكبار

The zebrafish model has emerged as a relevant system to study kidney development, regeneration and disease. Both the embryonic and adult zebrafish kidneys ...