C$%)*$* =+ /+*0+1(, 23,314)$
5G=$'-*(#H(*F%$ .$% #*(-30,$% 6+==(I"B$%: ;B0=0$) .$% +,,3$% JKLM
!"#$% &'( )*'+,'*( +-*.$'$*( +/012$0-,*'( -))0,.$1( 30- 41%15.$' &'( )/)$0-5/%(
!6,78*'%9 )-* 0'$* (1.$'%2' &#-2,&'( -+,%1(:2' .$, '%9*-;%' &'( 2<-*4'( %'='( /$ &'( >/*+'( &,71*'%9'(
!"'( &,71*'%9( -0080'( +,4*'%9 3&'( ?,9'(('( &,71*'%9'( 39*-?'*( 0'( 4'0(
!
Avantage :
$%' 4*-%&' .$-%591 &' &/%%1'( )/$?-,9 @9*' -22$+$01' )/$* &' %/+A*'$('( '()82'(
!
Inconvénient :
?-*,-5/% 41%15.$' 2-2<1'
B/+/CD4/9'( B'9'*/CD4/9'(
E00'0'FG
E00'0'FH
E00'0'FI
88
Géné$que moléculaire des popula$ons
C$%)*$* =+ /+*0+1(, 23,314)$
•Polymorphismes de longueur des fragments de restric6on (RFLP) —fin des
années 1970
!"'( '%CD+'( &' *'(9*,25/% *'2/%%-,(('%9 &'( (1.$'%2'( ()12,J.$'( K41%1*-0'+'%9 &'
L: M /$ NA-('(O '9 2/$)'%9 0#E6P '%9*' &'( (,9'( )*12,(
!
EX : HaeIII:
M#QRRSTTQI#UFFF
AlwI:
M#QRREVSTQI#UFFF
EcoRI:
M#QRSEEVVTQI#F
KWS#F,%&,.$' 0'F(,9'F&'F2/$)$*'O
!X-*,-5/%F&-%(F0'(F(,9'(F&'F2/$)$*'
!
EX:
REEVVTF?(YFRVEVVTFK('$0 0'F)*'+,'*F-0080' '(9 2/$)1F)-*FZ2/[\O
!
Électrophorèse :
0'( >*-4+'%9( &' 9-,00'( &,71*'%9'( +,4*'%9 3&'( ?,9'(('( &,71*'%9'(
&-%( 0' 4'0 K0'( >*-4+'%9( )0$( )'59( +,4*'%9 )0$( *-),&'+'%9O
!
E?-%9-4' ]
)0$(,'$*( 2'%9-,%'( &#'%CD+'( &' *'(9*,25/% &,()/%,A0'(
!
\%2/%?1%,'%9 ]
(D(98+' &' +-*.$'$*( &/+,%-%9( ^?-*,-5/% 2-2<1'
89
Géné$que moléculaire des popula$ons