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U etogo termina sushestvuyut i drugie znacheniya sm Gen znacheniya V drugom yazykovom razdele est bolee polnaya statya Gene angl Gen dr grech genos rod v klassicheskoj genetike nasledstvennyj faktor kotoryj nesyot informaciyu ob opredelyonnom priznake ili funkcii organizma i kotoryj yavlyaetsya strukturnoj i funkcionalnoj edinicej nasledstvennosti V takom kachestve termin gen byl vvedyon v 1909 godu datskim botanikom fiziologom rastenij i genetikom Vilgelmom Johannsenom Shema transkripcii DNK Posle otkrytiya nukleinovyh kislot v kachestve nositelya nasledstvennoj informacii opredelenie gena izmenilos i gen stali opredelyat kak uchastok DNK u nekotoryh virusov uchastok RNK zadayushij posledovatelnost monomerov v polipeptide libo v funkcionalnoj RNK Po mere nakopleniya svedenij o stroenii i rabote genov opredelenie ponyatiya gen prodolzhalo izmenyatsya odnako v nastoyashee vremya ne sushestvuet universalnogo opredeleniya gena kotoroe udovletvorilo by vseh issledovatelej Odno iz sovremennyh opredelenij gena zvuchit sleduyushim obrazom gen predstavlyaet soboj posledovatelnost DNK sostavlyayushie segmenty kotoroj ne obyazatelno dolzhny byt fizicheski smezhnymi Eta posledovatelnost DNK soderzhit informaciyu ob odnom ili neskolkih produktah v vide belka ili RNK Produkty gena funkcioniruyut v sostave geneticheskih regulyatornyh setej rezultat raboty kotoryh realizuetsya na urovne fenotipa Sovokupnost genov organizma sostavlyayut genotip Genotip naryadu s faktorami okruzhayushej sredy i razvitiem opredelyayut kakim budet fenotip Peredacha genov potomstvu yavlyaetsya osnovoj nasledovaniya fenotipicheskih priznakov Bolshinstvo biologicheskih priznakov yavlyaetsya poligennym to est nahoditsya pod vliyaniem mnogih genov Geny mogut izmenyatsya v rezultate mutacij izmenyayushih posledovatelnost DNK Vsledstvie mutacij v populyacii geny sushestvuyut v razlichnyh variantah nazyvaemyh allelyami Raznye alleli gena mogut kodirovat razlichayushiesya versii belka chto mozhet proyavlyatsya fenotipicheski Geny naryadu s uchastkami DNK ne soderzhashimi genov vhodyat v sostav genoma predstavlyayushego soboj ves nasledstvennyj material organizma IstoriyaObnaruzhenie genov kak diskretnyh nositelej nasledstvennosti Gregor Mendel Eksperimentalnye dokazatelstva nalichiya diskretnyh faktorov nasledstvennosti vpervye byli predstavleny v 1865 godu Gregorom Mendelem v doklade na zasedanii Obshestva estestvoispytatelej v Brno V 1866 godu doklad byl opublikovan v pechatnom vide Gregor Mendel izuchal nasledovanie priznakov u goroha kolichestvenno otslezhivaya chastotu priznakov u roditelskih rastenij i u potomstva V skreshivaniyah rastenij s razlichnymi priznakami on proanaliziroval bolee 8000 rastenij V etih eksperimentah Mendel prodemonstriroval nezavisimoe nasledovanie priznakov razlichie mezhdu dominantnymi i recessivnymi priznakami razlichie mezhdu geterozigotami i gomozigotami a takzhe yavlenie preryvistogo nasledovaniya Rezultaty svoih eksperimentov on opisal matematicheski i interpretiroval ih predpolozhiv chto sushestvuyut diskretnye nesmeshivaemye v potomstve faktory nasledstvennosti Do raboty Mendelya dominiruyushej koncepciej v obyasnenii zakonomernostej nasledovaniya byla koncepciya kotoraya predpolagala chto priznaki roditelej u potomkov smeshivayutsya analogichno smeshivaniyu zhidkostej Etoj koncepcii sleduet teoriya pangenezisa razrabotannaya Charlzom Darvinom v 1868 godu dva goda spustya posle publikacii rezultatov Mendelya V etoj teorii Darvin predpolozhil sushestvovanie ochen melkih chastic nazvannyh im gemmulami kotorye smeshivayutsya vo vremya zachatiya Statya Mendelya ostalas prakticheski nezamechennoj posle eyo publikacii v 1866 godu no ona poluchila vtoroe rozhdenie v konce XIX veka blagodarya Hugo de Frizu Karlu Korrensu i Erihu fon Chermaku kotorye prishli k analogichnym vyvodam v svoih sobstvennyh issledovaniyah V chastnosti v 1889 godu Hugo de Friz opublikoval svoyu knigu Intracellular Pangenesis v kotoroj on postuliroval chto raznye priznaki imeyut sobstvennye nasledstvennye nositeli i chto nasledovanie specificheskih chert u organizmov proishodit pri pomoshi chastic De Fris nazval eti edinicy pangenami Pangens na nemeckom yazyke ispolzovav chast nazvaniya teorii pangeneza Darvina V 1909 godu Vilgelm Johannsen vvel termin gen a Uilyam Bejtson termin genetika v to vremya kak Eduard Strasburger vse eshyo ispolzoval termin pangen dlya oboznacheniya osnovnoj fizicheskoj i funkcionalnoj edinicy nasledstvennosti Otkrytie DNK v kachestve nositelya geneticheskoj informacii Eksperimenty provedyonnye v 40 e gody amerikanskimi bakteriologami iz Rokfellerovskogo instituta pod rukovodstvom O Everi pokazali chto molekulyarnym hranilishem geneticheskoj informacii yavlyaetsya DNK V rabotah po geneticheskoj transformacii pnevmokokkov bylo pokazano chto peredacha priznakov ot odnih bakterij k drugim proishodit pri pomoshi tolko odnogo veshestva DNK Ni belok ni drugie himicheskie komponenty kletki etim svojstvom ne obladali V 1953 godu pri pomoshi rentgenovskoj kristallografii Rozalind Franklin i Moris Uilkins poluchili vysokokachestvennye snimki struktury DNK Eti snimki pomogli Dzhejmsu D Uotsonu i Frensisu Kriku sozdat model molekuly dvucepochechnoj spirali DNK i sformulirovat gipotezu mehanizma geneticheskoj replikacii V nachale 1950 h godov preobladalo mnenie chto geny v hromosome dejstvuyut kak otdelnye obekty nerazdelimye putem rekombinacii i raspolozhennye kak busy na verevochke Eksperimenty Sejmura Benzera s ispolzovaniem mutantov defektnyh bakteriofagov v oblasti angl 1955 1959 pokazali chto otdelnye geny imeyut prostuyu linejnuyu strukturu i veroyatno ekvivalentny linejnomu secheniyu DNK V sovokupnosti etot obyom issledovanij ustanovil centralnuyu dogmu molekulyarnoj biologii kotoraya utverzhdaet chto belki transliruyutsya s RNK kotoraya transkribiruetsya s DNK Eta dogma s teh por kak bylo pokazano imeet isklyucheniya takie kak obratnaya transkripciya v retrovirusah Sovremennoe issledovanie genetiki na urovne DNK izvestno kak molekulyarnaya genetika V 1972 godu Uolter Fajers i ego komanda pervymi opredelili posledovatelnost gena posledovatelnost belka obolochki angl Posleduyushee razvitie sekvenirovaniya DNK s metodom Sengera v 1977 godu Frederikom Sangerom uluchshilo effektivnost sekvenirovaniya i prevratilo ego v rutinnyj laboratornyj instrument Avtomatizirovannaya versiya metoda Sangera ispolzovalas na rannih etapah proekta Genom cheloveka Sovremennyj sintez i ego preemniki Osnovnaya statya Sinteticheskaya teoriya evolyucii Teorii razrabotannye v nachale XX veka dlya integracii mendelevskoj genetiki s darvinovskoj evolyuciej nazyvayutsya sovremennym sintezom terminom vvedennym Dzhulianom Haksli Evolyucionnye biologi vposledstvii modificirovali etu koncepciyu takuyu kak angl Dzhordzha Uilyamsa na evolyuciyu On predlozhil evolyucionnuyu koncepciyu gena kak estestvennogo otbora s opredeleniem to chto razdelyaet i rekombiniruet s zametnoj chastotoj 24 S etoj tochki zreniya molekulyarnyj gen transkribiruetsya kak edinoe celoe a evolyucionnyj gen nasleduetsya kak edinoe celoe Svyazannye idei podcherkivayushie centralnuyu rol genov v evolyucii byli populyarizirovany Richardom Dokinzom Molekulyarnaya osnovaSm takzhe DNK Himicheskaya struktura fragmenta dvojnoj spirali DNK Fragment sostoit iz chetyryoh sparennyh osnovanij CG AT GC TA Cepi saharo fosfatnogo ostova orientirovany v protivopolozhnyh napravleniyah Osnovaniya napravleny vnutr i svyazany vodorodnymi svyazyami s osnovaniyami protivopolozhnoj cepi DNK Geneticheskaya informaciya u podavlyayushego bolshinstva organizmov zakodirovana v dlinnyh molekulah DNK DNK sostoit iz dvuh spiralno zakruchennyh polimernyh cepej monomerami kotoryh sluzhat chetyre nukleotida dAMF dGMF dCMF i dTMF Nukleotidy v DNK sostoyat iz pyatiuglerodnogo sahara 2 dezoksiribozy fosfatnoj gruppy i odnogo iz chetyryoh azotistyh osnovanij adenina citozina guanina i timina 2 1 Azotistoe osnovanie svyazano glikozidnoj svyazyu s pyatiuglerodnym pentoznogo saharom v 1 polozhenii Ostovom cepej DNK sluzhit chereduyushayasya posledovatelnost pentoznyh saharov i fosfatov fosfatnye gruppy prisoedinyayutsya k saharu v 5 i 3 polozheniyah Nomera pozicij pentoznogo kolca otmecheny shtrihom dlya togo chtoby razlichat numeraciyu kolec v sahare i azotistom osnovanii Iz za himicheskogo sostava pentoznyh ostatkov cepi DNK imeyut napravlennost Odin konec polimera DNK soderzhit otkrytuyu gidroksilnuyu gruppu na dezoksiriboze v 3 polozhenii etot konec nazyvaetsya 3 konec Drugoj konec soderzhit otkrytuyu fosfatnuyu gruppu eto 5 konec Dve cepi niti dvojnoj spirali DNK orientirovany v protivopolozhnyh napravleniyah Sintez DNK v tom chisle pri replikacii DNK proishodit v napravlenii 5 3 potomu chto novye nukleotidy dobavlyayutsya posredstvom reakcii degidratacii kotoraya ispolzuet otkrytyj 3 gidroksil v kachestve nukleofila 27 2 Ekspressiya genov zakodirovannyh v DNK nachinaetsya s transkripcii nukleotidnoj posledovatelnosti DNK v posledovatelnost nukleotidov drugogo tipa nukleinovyh kislot RNK RNK ochen pohozha na DNK no eyo monomery soderzhat ribozu a ne dezoksiribozu Krome togo vmesto timina v RNK ispolzuetsya uracil Molekuly RNK yavlyayutsya odnocepochechnymi i menee stabilny chem DNK Geny v DNK a posle transkripcii i v tRNK predstavlyayut soboj prirodnyj shifr kod dlya sinteza belka Kazhdye tri nukleotida triplet kodiruyut odnu aminokislotu K primeru esli v gene 300 nukleotidov to v belke dolzhno byt 100 aminokislot Poetomu kod nazyvaetsya tripletnyj Pravilo po kotoromu opredelyaetsya kakomu tripletu sootvetstvuet kakaya aminokislota nazyvaetsya geneticheskim kodom Schityvanie geneticheskogo koda proishodit v ribosome vo vremya translyacii RNK v belok Geneticheskij kod pochti odinakov dlya vseh izvestnyh organizmov 4 1 Hromosoma Izobrazhenie normalnogo zhenskogo kariotipa poluchennogo pri pomoshi fluorescentnoj mikroskopii i metoda FISH DNK okrashena v krasnyj cvet a uchastki hromosom obogashyonnye po chislu lokalizovannyh v nih genov okrasheny v zelyonyj cvet Samye bolshie hromosomy primerno v 10 raz bolshe samyh malenkih Nasledstvennyj material organizma ili genom hranitsya v odnoj ili neskolkih hromosomah chislo kotoryh specifichno dlya vida Hromosoma sostoit iz odnoj ochen dlinnoj molekuly DNK kotoraya mozhet soderzhat tysyachi genov 4 2 Oblast hromosomy gde nahoditsya gen nazyvaetsya lokusom Kazhdyj lokus soderzhit opredelyonnyj allel gena Predstaviteli populyacii mogut otlichatsya po allelyam gena nahodyashimsya v odinakovyh lokusah hromosom Bolshinstvo eukarioticheskih genov hranyatsya v neskolkih linejnyh hromosomah Hromosomy upakovany v yadre v komplekse s belkami hromatina Naibolee mnogochislennymi belkami hromatina yavlyayutsya gistony kotorye formiruyut belkovuyu globulu nazyvaemuyu nukleosomoj DNK obvivaetsya vokrug nukleosom chto predstavlyaet soboj pervyj uroven upakovki DNK v hromosome 4 2 Raspredelenie nukleosom vdol DNK a takzhe himicheskie modifikacii samih gistonov reguliruyut dostupnost DNK dlya regulyatornyh faktorov uchastvuyushih v replikacii transkripcii translyacii i reparacii Pomimo genov eukarioticheskie hromosomy soderzhat takzhe sluzhebnye posledovatelnosti obespechivayushie stabilnost i vosproizvedenie hromosom a takzhe ih raspredelenie mezhdu dochernimi kletkami v mitoze Eto telomery sajty iniciacii replikacii i centromera sootvetstvenno 4 2 Funkcionalnye opredeleniyaEtot razdel slishkom korotkij Pozhalujsta uluchshite i dopolnite ego Trudno tochno opredelit v kakuyu chast posledovatelnosti DNK vhodit gen Osnovnye harakteristiki genaV molekulyarnoj biologii ustanovleno chto geny eto uchastki DNK nesushie kakuyu libo celostnuyu informaciyu o stroenii odnoj molekuly belka ili odnoj molekuly RNK kotorye opredelyayut razvitie rost i funkcionirovanie organizma Kazhdyj gen harakterizuetsya ryadom specificheskih angl takih kak promotory kotorye prinimayut uchastie v regulirovanii funkcii gena Regulyatornye posledovatelnosti mogut nahoditsya kak v neposredstvennoj blizosti ot otkrytoj ramki schityvaniya kodiruyushej belok ili nachala posledovatelnosti RNK kak v sluchae s promotorami tak nazyvaemye cis regulyatornye elementy angl cis regulatory elements tak i na rasstoyanii mnogih millionov par osnovanij nukleotidov kak v sluchae s enhanserami insulyatorami i supressorami inogda klassificiruemye kak trans regulyatornye elementy angl trans regulatory elements To est ponyatie gena ne ogranicheno tolko kodiruyushim uchastkom DNK Gen predstavlyaet soboj bolee shirokuyu koncepciyu vklyuchayushuyu v sebya i regulyatornye posledovatelnosti Iznachalno termin gen poyavilsya kak teoreticheskaya edinica peredachi diskretnoj nasledstvennoj informacii Istoriya biologii pomnit spory o tom kakie molekuly mogut yavlyatsya nositelyami nasledstvennoj informacii Schitalos chto takimi nositelyami mogut byt tolko belki tak kak ih stroenie 20 aminokislot pozvolyaet sozdat bolshe variantov chem DNK kotoraya sostoit vsego iz chetyryoh vidov nukleotidov Odnako eksperimentalno dokazano chto imenno DNK soderzhit v sebe nasledstvennuyu informaciyu chto bylo vyrazheno v vide centralnoj dogmy molekulyarnoj biologii DNK RNK belok Geny mogut podvergatsya mutaciyam sluchajnym ili celenapravlennym izmeneniyam posledovatelnosti nukleotidov v cepi DNK Mutacii mogut privodit k izmeneniyu posledovatelnosti a sledovatelno izmeneniyu biologicheskih harakteristik belka ili RNK Rezultatom mozhet stat izmenyonnoe ili dazhe anormalnoe funkcionirovanie organizma Takie mutacii v ryade sluchaev yavlyayutsya patogennymi tak kak ih rezultatom yavlyaetsya zabolevanie ili letalnymi na embrionalnom urovne Daleko ne vse izmeneniya posledovatelnosti nukleotidov privodyat k izmeneniyu struktury belka blagodarya effektu vyrozhdennosti geneticheskogo koda ili k sushestvennomu izmeneniyu posledovatelnosti i ne yavlyayutsya patogennymi V chastnosti genom cheloveka harakterizuetsya odnonukleotidnymi polimorfizmami i variaciyami chisla kopij angl copy number variations takimi kak delecii i duplikacii kotorye sostavlyayut okolo 1 vsej nukleotidnoj posledovatelnosti cheloveka Odnonukleotidnye polimorfizmy v chastnosti opredelyayut razlichnye alleli odnogo gena Molekulyarnaya evolyuciyaOsnovnaya statya Molekulyarnaya evolyuciya Mutaciya Replikaciya DNK po bolshej chasti chrezvychajno tochna odnako oshibki mutacii sluchayutsya 7 6 Chastota oshibok v eukarioticheskih kletkah mozhet sostavlyat vsego 10 8 v nukleotide na replikaciyu togda kak dlya nekotoryh RNK virusov ona mozhet dostigat 10 3 Eto oznachaet chto v kazhdoe pokolenie kazhdyj chelovek v genome nakaplivaet okolo 30 novyh mutacij Nebolshie mutacii mogut byt vyzvany replikaciej DNK i posledstviyami povrezhdeniya DNK i vklyuchayut tochechnye mutacii v kotoryh izmenyaetsya odno osnovanie i mutacii so sdvigom ramki v kotoryh odno osnovanie vstavlyaetsya ili udalyaetsya Lyubaya iz etih mutacij mozhet izmenit gen po missens izmenit kod dlya kodirovaniya drugoj aminokisloty ili po nonsens prezhdevremennyj stop kodon Bolshie mutacii mogut byt vyzvany oshibkami v rekombinacii chtoby vyzvat hromosomnye anomalii vklyuchaya dublirovanie deleciyu peregruppirovku ili inversiyu bolshih uchastkov hromosomy Krome togo mehanizmy vosstanovleniya DNK mogut vnosit mutacionnye oshibki pri vosstanovlenii fizicheskogo povrezhdeniya molekuly Vosstanovlenie dazhe s mutaciej yavlyaetsya bolee vazhnym dlya vyzhivaniya chem vosstanovlenie tochnoj kopii naprimer pri vosstanovlenii dvuhcepochechnyh razryvov 5 4 Kogda v populyacii vida prisutstvuet neskolko razlichnyh allelej gena eto nazyvaetsya polimorfizm Bolshinstvo razlichnyh allelej funkcionalno ekvivalentny odnako nekotorye alleli mogut vyzyvat razlichnye Samyj rasprostranennyj allel gena nazyvaetsya dikim tipom a redkie alleli mutantami Geneticheskie razlichiya v otnositelnyh chastotah razlichnyh allelej v populyacii obuslovleny kak estestvennym otborom tak i geneticheskim drejfom Allel dikogo tipa ne obyazatelno yavlyaetsya predkom menee rasprostranennyh allelej i ne obyazatelno bolee prisposoblena Kolichestvo genov i kolichestvo genov kotorye on soderzhit znachitelno variruyut u taksonomicheskih grupp Naimenshij genom vstrechayutsya u virusov i viroidov kotorye dejstvuyut kak odin nekodiruyushij gen RNK I naoborot rasteniya mogut imet ochen bolshie genomy v rise soderzhatsya bolee 46 000 genov kodiruyushih belok Obshee kolichestvo kodiruyushih belok genov proteoma Zemli kotoroe ocenivalos v 2007 godu v 5 mln posledovatelnostej k 2017 godu bylo snizheno do 3 75 mln Gennaya inzheneriyaOsnovnaya statya Gennaya inzheneriya Gennaya inzheneriya eto metody modifikacii geneticheskogo materiala dlya izmeneniya svojstv zhivogo organizma S 1970 h godov bylo razrabotano specialno prednaznachennyh dlya dobavleniya udaleniya i redaktirovaniya genov v virusah bakteriyah rasteniyah gribah i zhivotnyh vklyuchaya cheloveka Nedavno razrabotannye metody genomnoj inzhenerii ispolzuyut inzhenernye nukleaznye fermenty dlya sozdaniya celevoj reparacii DNK v hromosome chtoby libo razrushit libo otredaktirovat gen v processe reparacii iskusstvenno vnesyonnogo razryva DNK Svyazannyj termin sinteticheskaya biologiya inogda ispolzuetsya dlya oboznacheniya obshirnoj discipliny gennoj inzhenerii organizma Gennaya inzheneriya v nastoyashee vremya yavlyaetsya rutinnym instrumentom pri rabote s modelnymi organizmami Naprimer geny legko dobavlyayutsya k bakteriyam a linii angl myshej s narushennoj funkciej opredelyonnogo gena ispolzuyutsya dlya issledovaniya funkcii etogo gena Mnogie organizmy byli geneticheski modificirovany dlya primeneniya v selskom hozyajstve promyshlennoj biotehnologii kletochnoj biologii i medicine U mnogokletochnyh organizmov obychno modificiruetsya embrion kotoryj vyrastaet vo vzroslyj geneticheski modificirovannyj organizm Odnako genomy kletok vzroslogo organizma mozhno redaktirovat s ispolzovaniem metodov gennoj terapii dlya lecheniya geneticheskih zabolevanij Svojstva genadiskretnost nesmeshivaemost genov stabilnost sposobnost sohranyat strukturu labilnost sposobnost mnogokratno mutirovat mnogie geny sushestvuyut v populyacii vo mnozhestve molekulyarnyh form v genotipe diploidnyh organizmov tolko dve formy gena kazhdyj gen kodiruet svoj priznak plejotropiya mnozhestvennyj effekt gena ekspressivnost stepen vyrazhennosti gena v priznake penetrantnost chastota proyavleniya gena v fenotipe amplifikaciya uvelichenie kolichestva kopij gena istochnik ne ukazan 3578 dnej KlassifikaciyaStrukturnye geny geny kodiruyushie informaciyu o pervichnoj strukture belka Raspolozhenie nukleotidnyh tripletov v strukturnyh genah kollinearno posledovatelnosti aminokislot v polipeptidnoj cepi kodiruemoj dannym genom Sm takzhe statyu geny domashnego hozyajstva Funkcionalnye geny geny kotorye kontroliruyut i napravlyayut deyatelnost strukturnyh genov Sm takzheV rodstvennyh proektahZnacheniya v VikislovareMediafajly na Vikisklade Neposredstvenno rannie geny Alleli Genom Genoterapiya Realizaciya geneticheskoj informacii Epigenetika Replikaciya DNK RNK Geneticheskaya ekspertiza Geneticheskaya karta Biblioteka genovPrimechaniyaJohannsen W 1905 Arvelighedslaerens elementer The Elements of Heredity Copenhagen Rewritten enlarged and translated into German as Elemente der exakten Erblichkeitslehre Jena Gustav Fischer 1909 Scanned full text ot 30 maya 2009 na Wayback Machine Tarantul V Z Tolkovyj slovar po molekulyarnoj i kletochnoj biotehnologiiyu Russko anglijskij M Yazyki slavyanskoj literatury 2015 T 1 S 370 371 984 s ISBN 978 5 94457 249 3 Pearson H Genetics what is a gene angl Nature 2006 May vol 441 no 7092 P 398 401 doi 10 1038 441398a Bibcode 2006Natur 441 398P PMID 16724031 Pennisi E Genomics DNA study forces rethink of what it means to be a gene angl Science journal 2007 June vol 316 no 5831 P 1556 1557 doi 10 1126 science 316 5831 1556 PMID 17569836 Gericke Niklas Markus Hagberg Mariana Definition of historical models of gene 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