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Эволюция редактируемых генов митохондриального генома трипаносоматид

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Siep, M, K van Oosterum, H Neufeglise H van der Spek, and LA Grivell 2000 Mss5lp, a putative translational activator of cytochrome c oxidase subumt-1 (COX1) mRNA, is required for synthesis of Coxlp in Saccharomvces cerevisiae Curr Genet 37 213−220. Hirose T, H Fan, J Y Suzuki, T Wakasugi T Tsudzuki, H Kossel. and M Sugiura 1996 Occurrence of silent RNA editing in chloroplasts its species… Читать ещё >

Содержание

  • Список сокращений
  • Обзор литературы
  • Редактирование РНК: от вирусов до человека
  • Редактирование в царстве растений
  • Редактирование в митохондриях растений
  • Редактирование в пластидах растений
  • Редактирование в ядерном геноме растений
  • Редактирование у миксомицетов
  • Редактирование в царстве животных
  • Редактирование в митохондриях животных
  • Дезаминирование аденозина
  • Систематическое положение и особенности организации Ктеи>р1а5йс1а: уридиловое редактирование
  • Структура кинетопластного ассоциата
  • Механизм уридилового редактирования у трипаносоматид
  • Особенность уридилового редактирования — гРНК
  • Белки ЯЕСС, 20Э комплекс, модель ферментативного каскада
  • Редактирование гРНК в цис-положении: возможные истоки редактирования
  • Дополнительные факторы, не входящие в состав ЯЕСС
  • 3. '-5' полярность редактирования
  • Эволюция редактиуемых доменов криптогенов трипаносоматид
  • Ретропозиционная модель уменьшения размера редактируемого домена
  • Репликация кинетопластной ДНК и утрата классов миниколец
  • Функции редактирования РНК
  • Регуляция генной экспрессии на разных стадиях жизненного цикла
  • Альтернативное редактирование как источник генетического разнообразия
  • Редактирование — движущая сила адаптивной молекулярной эволюции
  • Материалы и методы
  • Объекты исследования
  • Культуры клеток
  • Реактивы
  • Ферменты
  • Синтетические олигонуклеотиды
  • Готовые наборы реактивов
  • Оборудование
  • Выделение РНК из культур клеток
  • Обратная транскрипция
  • Выделение кинетопластной ДНК из культуры клеток
  • Электрофоретическое разделение ДНК
  • Молекулярное клонирование
  • Компьютерная обработка последовательностей
  • Филогенетический анализ
  • Последовательности нуклеотидов, полученные в ходе работы
  • Результаты и обсуждение
  • Установление структуры криптогена N08?? а11асета л-/?. Vscl, Ьер (отопа$ соНо. чота, ЬерЮтопаз п&йт и Ащотопа$ с1еапе1 (НегреШтопая гоИтат)
  • Установление филогенетических отношений между ШаНасета $р. Лер1отопах соПозота, ЬерШтопая Angomonas с1еапе1 и другими видами
  • Криптогены с редукцией редактируемого домена
  • Группа криптогенов с консервативной структурой коротких РД
  • Криптогены с вариабельной первичной структурой, транскрипты которых редактируются по всей длине
  • Три типа структурной организации криптогенов трипаносоматид
  • ВЫВОДЫ

Эволюция редактируемых генов митохондриального генома трипаносоматид (реферат, курсовая, диплом, контрольная)

выводы.

1. По структуре и длине редактируемого домена криптогены митохондриального генома трипаносоматид могут быть объединены в три группы: 1) криптогены с редукцией длины редактируемого домена, 2) криптогены с короткими консервативными редактируемыми доменами и 3) криптогены с вариабельной первичной структурой, транскрипты которых редактируются по всей длине (вариабельные полностью редактируемые криптогены).

2. Виды, криптогены которых претерпевают определенную степень редукции длины РД (5' редактируемая форма, минимально редактируемый ген) объединяются на филогенетическом дереве в разные группы.

Редукция длины редактируемых доменов криптогенов А6, СОШ, №)8 происходит согласованно в группах 1Х¥и эндосимбионт-содержащих видов.

3. Структура криптогенов с короткими консервативными РД коррелирует с максикольцевым кодированием генов гРНК, необходимых для редактирования этих криптогенов.

4. Для полностью редактируемых криптогенов с вариабельной структурой характерны преимущественно миникольцевая локализация генов гРНК и альтернативное редактирование транскриптов.

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