species- Mus musculus Mouse Molecular Genetics David...
Transcript of species- Mus musculus Mouse Molecular Genetics David...
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species- Mus musculus
Mouse Molecular Genetics David Ornitz
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History of the laboratory mouseEomaia scansoria - ✴ a large mouse-like mammal ✴ the earliest representative of the
Eutherian (placental) lineage ✴ gave rise to all modern placental
mammals 75-125 million years ago
Genus Mus - ✴ established ~6 million years ago
Mus musculus (the house mouse) ✴ appeared as a distinct species
~8,000 BC
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Mus musculus - four main subspeciesMus musculus domesticus-arose in Western Europe, Mediteranean, Africa and Middle east.Mus musculus musculus-East Europe, Japan, Russia, Northern ChinaMus musculus castaneus-Southeast Asia, IndonesiaMus musculus bactrianus-Iran, Pakistan, India
Mus spretus Western Mediterranean short-tailed mouse
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The mouse as a genetic modelIdeal mammal for use by early geneticists - small size, relatively large litter size, rapid generation time
The mouse as a tool for genetics began in the early 1900‘sWilliam E. Castle, JBS Haldane andAbbie Lanthrop (Granby mouse farm)• established a mouse farm for pets, interesting coat colors and behavior• breeding experiments• establishment of mutant lines, ancestors of modern inbred strainsOther strains derived by Japanese, Chinese, and European mouse fanciers.
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“If you want to get mice with rare color by breeding do not take good dancing mice. They are harder to breed.”
Chingan Sodategusa (How to raise rare mice) Published by Zeniya Choubei in Kyoto in 1787
Early depiction of the mouse, one of the twelve animals of the Chinese zodiac, from a printed scroll, AD 877
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Ms Abbie Lathorp at Granby farm, 1913
Fancy mice become lab mice (~1900)
Letter from W. Castle concerning the mice used at Harvard, with mention waltzing mice received from Japan.
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A sequence-based variation map of 8.27 million SNPs in inbred mouse strains, 2007, Frazer et al., Nature
a, Musculus, castaneus and domesticus subspecies diverged from a common ancestor about one million years ago.
b, Subspecies molossinus is a more recent hybrid between musculus and castaneus. c, Eighteenth century, mouse fanciers in Japan and China inter-bred the Asian Mus
musculus subspecies to produce varieties of mice with different coat colors and behavioral characteristics.
d, Victorian England, ‘fancy’ mice, imported from Asia, were bred with local mice. In the early twentieth century, mating programs using a limited number of founding ‘fancy’ mice were started in the USA, giving rise to many of the modern classical strains.
e, Relative contributions of the Mus musculus subspecies to haplotypes in classical strains.
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Fancy Mice have been exhibited in Britain for more than 100 years. The Fancy started in the East End of London in the 1890's. The interest spread to the North of England where it became very popular in the mining communities. The National Mouse Club lays down the standards by which mice are judged. The LSCMRC is working on a library of photographs of all varieties of Fancy Mice and a digital library on the Mouse Fancy.
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Backed by two car barons, Edsel Ford (son of Henry) and Roscoe Jackson (head of Hudson Motorcar Company), Clarence Little set up Jackson Laboratory in Bar Harbor, Maine founded in 1929
C.C. Little
Jackson Laboratory
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M. musculus and M. spretus
✦ Never produce hybrids in nature.
✦ They are biochemically distinct.
✦ Their genomes are highly polymorphic.
✦ They can be bred in the laboratory. (However, the F1 males are sterile)
Extremely useful for genetic mapping studies.However, with the development of highly polymorphic SSLP markers, crosses to “wild” mice are usually no longer necessary.
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The Origin of Mouse GeneticsGenetic mapping in the mouse began with Haldane’s report(1915) of linkage between the pink-eye dilution and albino loci.
This linkage group was eventually assigned to mouse chromosome 7
This was only 2 years after the first report of genetic linkage in Drosophila.
Haldane, J. B. S., Sprunt, A.D. & Haldane,N.M. Reduplication in mice. J. Genet. 5, 133–135 (1915).
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Inbred strains of miceDefined by 20 or more generations of brother/sister matings.After 20 generations of inbreeding 98.6% of loci are homozygous.
The C57 strain is derived from female #57 from the Granby mouse farm around 1900.Now there are more that 400 inbred strains.
One driving force to establish inbred strains was to study genetics of tumor transplantation and cancer susceptibility. In 1948 Gorer and Snell described what is now known as the histocompatibility locus.
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←129/SV
←C57BL/6J
Beck JA, Lloyd S, Hafezparast M, Lennon-Pierce M, Eppig JT, Festing MFW, Fisher EMC. 2000. Genealogies of mouse inbred strains. Nature Genetics 24: 23-25.
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The mouse as a tool for genetics began in the early 1900‘s
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Recombinant Inbred Strains (RI)Strains formed by crossing two inbred strains, followed by 20 or more generations of brother/sister matings.
Congenic StrainsTwo strains that are genetically identical except at a single locus. (used to transfer a mutation onto a new genetic background)
Today’s classical inbred strains of mice can be considered recombinant inbred strains primarily derived from M. m. domesticus and M. m. musculus.
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SubstrainsBranches of an inbred strain that have known or probable genetic differences.
(1) Branches of a strain are separated before the 40th generation of inbreeding. (2) Branches of a strain have been maintained separately from other branches for more than 10 generations of inbreeding.
Example: C57B6 from different vendors are not equivalent (3) Genetic differences from other branches are discovered.
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Types of mutationsRecessive - an allele producing a phenotypic effect only in the absence of the wild-type alleleMost recessive mutations are loss of function mutations, Most deleterious mutations involve a deficiency of the defective gene.
(either amount or activity)
Dominant - an allele producing a phenotypic effect in the presence of a wild-type allele, often involves the production of a novel gene activity.Gain of function mutations are usually dominant.
Haplo - insufficient - reduction in gene activity below a threshold.
Dominant negative - a mutation that blocks the function or activity of the wild-type allele
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Types of alleles
Null - a mutant with a phenotype that produces no wild-type gene product or activity.
Amorph - similar to null but without a detectable phenotype.
Hypomorph - a mutant allele producing reduced, but not zero activity. Usually associated with a phenotype.
Neomorph - a dominant mutant gene producing a novel phenotypic effect.
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How do we identify new genes? new alleles?
Naturally occurring mutations
✴ spontaneous, chemically induced, radiation induced
✴ allows one to choose a phenotype of interest
✴ requires gene mapping, identification and cloning
✴ can lead to the discovery of completely novel genes
✴ can lead to a mouse model of a human disease
✴ the gene can be difficult to identify
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How do we identify new genes? -cont.
Induced random mutations
random DNA insertion (by product of transgenic mice, retrovirus insertion, transposon, ES cells)
enhancer trap or gene trap (splice acceptor)
✴ - the type of phenotype cannot be chosen
✴ - provides a sequence tag
✴ - requires gene mapping, identification, and cloning
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How do we identify new genes? -cont.
Random cDNA sequencing (ESTs)
✴ Provides a gene, but not necessarily a function.
✴ May miss genes that are expressed in very specific spatial and temporal locations.
✴ May identify gene families.
✴ A powerful tool in combination with gene targeting.
✴ May require gene mapping (there are still gaps in the genome sequence).
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How do we identify new genes? -cont.Gene identification from genomic sequence.
✴ Requires genomic sequence and gene identification algorithms.
✴ Not biased by gene expression patterns.
✴ May identify gene families.
✴ A potentially powerful tool in combination with gene targeting.
✴ May identify pseudogenes.
✴ May miss some genes or parts of genes.
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The mouse genome✦ 40 chromosomes (20 haploid chromosomes, 19, X, Y)
✦ Diploid DNA content, 2.7 x 109 bp (about 6.4 pg per nucleus)
✦ 8-10% of the genome is repeat sequence
✦ Estimated genetic haploid length is 1400CM, 1CM is 1.5x106 bp
✦ Over 90% of the mouse and human genomes can be partitioned
into corresponding regions of conserved synteny
✦ Approximately 80% of mouse genes have a single identifiable
orthologue in the human genome
✦ Draft sequence was completed in 2002 (Nature, Dec. 2002).
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37,311 Genes (including uncloned mutants) 28,983 Genes with nucleotide sequence data 25,066 Genes with protein sequence data 14,024 Genes with experimentally-based functional annotations 13,233 Genes with gene traps 13,185 Genes with expression assay results 85,345 Mapped genes/markers
Genome Length: 2,730,871,774
Mouse genome statistics
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Mapping genes
Classical genetic backcross−linkage mapping
Look for recombination and linkage between two genetic loci.
Example: Dominant white spotting and alfa feto protein.
Look at coat color (dominant white spotting) and electrophoretic migration (AFP)(or similarly look at an RFLP for the AFP gene)
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Linkage mapping
progenitor strains
progenitor strains
G1 back cross
recombination frequency is ameasure of genetic distance
50% 50%if tightly linked
Dominant-white spotting (W) locusencodes the c-kit proto-oncogene
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Linkage mapping can be used to map any mutation with a phenotype to any polymorphic marker or other mutation with a phenotype.
But this takes a long time and requires breeding.
Mouse tools to facilitate mapping:• Recombinant Inbred strains • Interspecific and intersubspecific crosses
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Recombinant Inbred (RI) strains
Start with two different inbred strains of mice.20 generations of brother-sister matings.Establish 30 RI mouse strains.
Polymorphisms between the parental progenitor strains become fixed in each RI line.
Each RI strain is unique.
The map position of novel genetic loci can be determined by matching their pattern of allelic polymorphisms to the strain distribution pattern pattern for the 30 RI strains.
Limitations in map resolution due to a finite number of strains
Advantages for large scale mapping - infinite amount of DNA
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Mapping withrecombinantinbred (RI) strains
brother-sister mating
G2
brother-sister mating20 generations
G20
RI line number
G1
progenitor strains
BXD cross
C57B6 DBA
A
B
C
DE
DBBDBBBD
BBBBBBDDDDBB
1234
B=C57BL/6J alleleD=DBA allele
strain dist ributionpattern
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RI strain distribution pattern
Example: Map an unknown gene, with RI strain distribution pattern BBDD.
A
B
C
DE
DBBDBBBD
BBBBBBDDDDBB
1234
B=C57BL/6J alleleD=DBA allele
strain dist ributionpattern
B=C57BL/6J alleleD=DBA allele
-maps near locus D
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BXD strain distribution pattern, mouse chromosome 14 BXD 1 2 5 6 8 9 11 12 13 14 15 16 18 19 20 21 22 23 24 25 27 28 29 30 31 32
D14Byu1 D D B D B D D B B B D D D D B D D B D B B D B B D DD14Hgu1 D D B D B D D B B B D D D D B D D B D B B B D B D DOdc-rs9 D D B D B D D B B *B D D D D B D D B D B B B D B D DP40-rs6 D D B D B D D B B B D D D D B D D B D B B B D B D D
Rarb D D B D B D D B B B D D D D B D D B D B B B D B D DPtprg B B D B D D B B B D D D D B B D D B D B B B D B D D
D14Nds1 . D B D B D D B B B D B D D B D D B B B B B D . . .Plau D D B D B D D B B B D B D D B D D B B B B B D B D D
D14Mit1 . D B D B D D B B B D D D D B D D B D B B B D . . .D14Mit2 . D B D B D D B B B D B D D B D D B B B B B D . . .D14Pas1 B D B D D D D B B D D D B D B . D B B B B B D B D D
Glud B D B B . D D B B D D B . D . B B B B B . B D B D DMtv11 B D B D D D D B B D D D B D B B D B *B D B B D B D D
Ms15-7 B D B D D D D B B D D D D D B B D . B B B B D B D DMs6-5 B D . D D D D D . D B D D D . . B . B B B B D B D DNrl B D B D D D D D B D D D D D B B B B B B B B D B D DNp B D B D D D D D B D D D D D B B B B B B B B D B D D
Tcra B D B D D D D D B D D D D D B B B B B B B B D B D DXmv19 B D B D D D D D B D D D D D B B B B B B B B D B D D
D14Byu2 B D B D D D D D B D D D D D B B B B . B B . D . D DAng B D B D D D D D B D D D D D B B B B B B B B D B D D
D14Byu3 B D B D D D D D B D D D D D B B B B B B B B D B D DRib1 B D B D D D D D B D D D D D B B B B B B B B D B D D
D14Byu4 B D B D D D D D B D D D D D B B B B B B B B D B D DMcpt1 B D B D D D D D B D D D D D B B D B B B B B D B D DMcpt4 B D B D D D D D B D D D D D B B D B B B B B D B D DMcpt5 B D B D D D D D B D D D D D B B D B B B B B D B D DMyhca B D B D D D D D B D D D D D B B B B B B B B D B D DCtla6 B D B D D D D D B D D D D D B B D B B B B B D B D D
D14Mit5 . D B D D D D B B D D D D D B B D B B B B B D . . .D14Mit6 . D B D D D D B B D D D B D B B D B B D B B D . . .
Raftk B D B D D D D B B D D D B D B B D B B D B B D B B DD14Byu5 B D B D D D D B B D D D B D B B D B B D B B D B B D
Gnrh B D B D D D D B B D D D B D B B D B B D B B D B B DEs10 B D B D D D D B B D D B B D B B B B B D B B D D . DFor5 B D B D D D D B B D D B B D B B B B B D B B D D . .Rb1 B D B D D D D B B D D B B D B . B B B D B B D . . D
Iapls3-15 B D B D D D D B B D D B B D B B B B B D B B D D B DTstap198-14 B D B D D D D B B D D B B D B B B D B D B B D D B B
D14Mc1 B D B D D D D B B D D D B D B B B D B D B B D D B DIapls2-12 B D B D D D D B B D D B B D B B B D B D B B D D B BD14Mit7 . D B D D D D B B D D . B D B B B D B D B B D . . .
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Interspecific and intersubspecific crosses
Crosses between laboratory strains and distantly related species of Mus.
Advantage: Most sequences are polymorphic.
M. spretus (inter-specific):Small inversions may suppress recombination in some regions.Males are sterile so you cannot do an intercross.
M. m. castaneus (inter-sub specific)More closely related (sub species)
Still has a high degree of polymorphisms.Both F1 sexes are fertile so you can do an intercross.
Resolution is high - large numbers of animals,but DNA is limited to that obtained from one mouse.
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BSSpolymorphismdistribution panel
A SBSSSBBB BSS.SB
B SBSSSBBB BSSBSBx
C SBSBSBBB BSSBSB
D SBSBSBBB BSSBSBx x x
E BBSBBBBB BSSBBB
12345678 901234
Mapping with backcross mapping panels
progenitorstrains
C57B6 X M. spretus
C57B6 M. spretus
G1
a
b
c
d
E
a
b
c
d
e
1
A
B
C
D
E
a
b
c
d
e
2
a
b
c
d
e
a
b
c
d
e
3
a
b
C
D
E
a
b
c
d
e
4
a
b
c
d
E
a
b
c
d
e
5
A
B
C
D
E
a
b
c
d
e
6
A
B
C
D
E
a
b
c
d
e
7
A
B
C
D
E
a
b
c
d
eX
X
X8 ....94
BS
M. spretus
BSS
X
X
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11111111 11111111 11111111Locus 111111 22222222 33333333 44444444 55555555 66666666 77777777 88888888 99999999 00000000 11111111 22222222 R/N
CDEFGH ABCDEFGH ABCDEFGH ABCDEFGH ABCDEFGH ABCDEFGH ABCDEFGH ABCDEFGH ABCDEFGH ABCDEFGH ABCDEFGH ABCDEFGH
D14Sh1 SBSSBS SSBSBBSS BSBSBBSB BSBBBSBS SBSBBSBB SBSBSBBB SSBSSSBB SSBBBSBB SBSSSBSS BBSBSSSB SBBBBSSS BSSBBBBSx x x 3/93
D14Hun3 SBSSBS SSBSBBSS BSBSBBSB BSBBBSBS SBSBBSBB SBSBSBBB SSBSSSBB SSBBBSBB SBSSSBBS SBSBSSSB .BBBBSSS SSSBBBBS 0/93D14Hun4 SBSSBS SSBSBBSS BSBSBBSB BSBBBSBS SBSBBSBB SBSBSBBB SSBSSSBB SSBBBSBB SBSSSBBS SBSBSSSB .BBBBSSS SSSBBBBS
x x 2/91D14Xrf363 SBSSBS SSBSBBSS BSBSBBSB BSBBBSBS SBSBBSBB SBSBS.BB SSBSSSBB .SBBBSBB SBSSSBBS BBSBSSSB SBBBBSSS BSSBBBBS 0/92D14Mit11 SBSSBS SSBSBBSS BSBSBBSB BSBBBSBS SBSBBSBB SBSBSBBB SSBSSSBB SSBBBSBB SBSSSBBS BBSBSSSB SBBBBSSS BSSBBBBS
x 1/94D14Mit132 SBSSBS SSBSBBSS BSBSBBSB BSBBBSBS SBSBBSBB SBSBSBBB SSBSSSBS SSBBBSBB SBSSSBBS BBSBSSSB SBBBBSSS BSSBBBBS 0/80Ptma-rs4 SBSSB. .SBSBBS. BSBSBBS. BSBBBSB. SBSBBSBB SBSBSBBB ..BSSSBS SSBBBS.B SBSSSB.S BBSBSS.B SBBBB..S BSSBB..S
x x 2/73Anx7 SBSSBS SSBSB.SS BS.SB.SB BSBBBSB. BBSBBSB. SBSBSBBB SSBSSSBS SSBBBSBB .BSSSBBS BBSBSSSB BBBBBSSS .SSB.B.S 0/85Plau SBSSBS SSBSBBSS BSBSBBSB BSBBBSBS BBSBBSBB SBSBSBBB SSBSSSBS SSBBBSBB SBSSSBBS BBSBSSSB BBBBBSSS BSSBBBBS 0/94Vdac2 SBSSBS SSBSBBSS BSBSBBSB BSBBBSBS BBSBBSBB SBSBSBBB SSBSSSBS SSBBBSBB SBSSSBBS BBSBSSSB BBBBBSSS BSSBBBBS 0/94D14Mit2 SBSSBS SSBSBBSS BSBSBBSB BSBBBSBS BBSBBSBB SBSBSBBB SSBSSSBS SSBBBSBB SBSSSBBS BBSBSSSB BBBBBSSS BSSBBBBS 0/94D14Bir1 SBSSBS SSBSBBSS BSBSBBSB BSBBBSBS BBSBBSBB SBSBSBBB SSBSSSBS SSBBBSBB SBSSSBBS BBSBSSSB BBBBBSSS BSSBBBBS 0/94D14Bir2 SBSSBS SSBSBBSS BSBSBBSB BSBBBSBS BBSBBSBB SBSBSBBB SSBSSSBS SSBBBSBB SBSSSBBS BBSBSSSB BBBBBSSS BSSBBBBS
x x 2/94D14Hun5 SBSSBS SSBSBBSS BBBSBBSB BSBBBSBS BBSBBSBB BBSBSBBB SSBSSSBS SSBBBSBB SBSSSBBS BBSBSSSB BBBBBSSS BSSBBBBS 0/91D14Hun6 SBSSBS SSBSBBSS BBBSBBSB BSBBBSBS BBSBBS.B BBSBSB.B SSBSSSBS SSBBBSBB SBSSSBBS BBSBSSSB .BBBBSSS BSSBBBBS
x 1/88D14Hun7 SBSSBS .SBS.BSS BBBSBBSB BSBBBSBS BBSBBSBB BBSBSB.S SSBSSSBS SSBBBSBB SBSSSBBS BBSBSSSB ..BBBSSS BSSBBBBS
x x x 3/80Wnt5a SBSSBS SSBSBBSS BBBSBBSB BSBBBSBS BBSBBSSB BBSBSBBB SSBSSSBS SSBBBSBB SBSSSBBS BBSBSSSB BBBBBBS. ........ 0/80D14Abb1e SBSSBS SSB.BB.S BBB.BBSB BSBBBSBS BBSBBSSB BBSBSBBB SSBSSSBS SSBBBSBB SBSSSBBS BBSB..SB BBBBBBSS BSSBB...
x x 2/83Chat SBSSBS SSBSBBSS BBBSBBSB BSBBBSBS ..SBSSSB BBSBSBBB SSBSSSBS BSBBBSBB SBSSSBBS BBSBSSSB BBBBBB.S BSSBBBBS 0/91Pkcd SBSSBS SSBSBBSS BBBSBBSB BSBBBSBS BBSBSSSB BBSBSBBB SSBSSSBS BSBBBSBB SBSSSBBS BBSBSSSB BBBBBBSS BSSBBBBS 0/93D14Xrf373 SBSSBS SSBSBBSS BBBSBBSB BSBBBSBS BBSBSSSB BBSBSBBB SSBSSSBS BSBBBSBB SBSSSBBS BBSBSSSB BBBBBB.S BSSBBBBS 0/92D14Xrf434 SBSSBS SSBSBBSS B.BSBBSB BSBBBSBS BBSBSSSB BBSBSBBB SSBSSSBS BSBBBSBB SBSSSBBS BBSBSSSB BBBBBBSS BSSBBBBS 0/92D14Bir4 SBSSBS SSBSBBSS BBBSBBSB BSBBBSBS BBSBSSSB .BSBSBBB SSBSSSBS BSBBBSBB SBSSSBBS BBSBSSSB BBBBBBSS BSSBBBBS
x 1/93D14Mit3 SBSSBS SSBSBBSS BBBSBBSB BSBBBSBS BBSBSSSB BBSBSBBB SSBSSSBS BSBBBSBB SBSSSBBB BBSBSSSB BBBBBBSS BSSBBBBS
0/94D14Bir5 SBSSBS SSBSBBSS BBBSBBSB BSBBBSBS BBSBSSSB BBSBSBBB SSBSSSBS BSBBBSBB SBSSSBBB BBSBSSSB BBBBBBSS BSSBBBBS
0/94D14Trk1 SBSSBS SSBSBBSS BBBSBBSB BSBBBSBS BBSBSSSB BBSBSBBB SSBSSSBS BSBBBSBB SBSSSBBB BBSBSSSB BBBBBBSS BSSBBBBS
x 1/94Mbl1 SBSSBS SSBSBBSS BBBSBBSB BSBBBSBS BBSBSSSB BBSBSBBB SSBSSSBS BSBBBSBB SBSSSBBB BBSBSSSB BBBSBBSS BSSBBBBS
0/94Sftp1 SBSSBS SSBSBBSS BBBSBBSB BSBBBSBS BBSBSSSB BBSBSBBB SSBSSSBS BSBBBSBB SBSSSBBB BBSBSSSB BBBSBBSS BSSBBBBS
0/94Sftp4 SBSSBS SSBSBBSS BBBSBBSB BSBBBSBS BBSBSSSB BBSBSBBB SSBSSSBS BSBBBSBB SBSSSBBB BBSBSSSB BBBSBBSS BSSBBBBS
x x x x 4/94D14Bir7 SBSBBS SSBSBBSS BBBSBBSB BSBBBSBS BBSBSSSB BBSBSBBB SSBSSSBS BSBBBSSB SBSSSBBB BBSBSBSB BBBSBBSS BSSBBBBB
x 1/88D14Hun8 SBSBBS SSBSBBSS BBBSBBSB BSBBBSBS BBSBSSSB BBBBSBBB SSBSSSBS BSBBBSSB SBSSSBBB xBSBSBSB ..BSBBSS .x.BBBBB
x 1/87D14Hun9 SBSBBS SSBSBBSS BBBSBBSB BSBBBSBS BBSBSSSB BBBBSBBB SSBSSSBS BSBBBSSB SSSSSBBB SBSBSBSB ..BSBBSS .BS.BBBB
x x 2/89D14Hun10 SBSBBS SSBSBBSS BBB.BBSB BSBBBSBS BBSBSSSB BBBBSBBB SSBSSSBS BSBBBSSB SBSSSBBB SBSBSBSB ..BSBBSS BSSBBBBB
0/90
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Mapping with anonymous DNA sequences
✴Simple sequence length polymorphisms (SSLP) also called STS (sequence tagged sites)
✴STRs, short tandem repeats about 100,000 randomly dispersed throughout the genome.
✴SNPs, single nucleotide polymorphisms occur every 500-1000 base pairs.
✴(CA)n repeats isolated by screening a small insert DNA library.
PCR to identify polymorphisms. di, tri or tetra-nucleotide repeats. ★ often polymorphic ★ suitable for typing virtually any mouse cross (interspecific, intersubspecific or between lab substrains)
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Ensembl SNP view page
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Genotyping with SSLPs
1,1 1,2 1,3 3,3 2,3 2,2
GATCACTGTTACGGCACACACACACACACACAAATTGCTAGCTACCGT
GATCACTGTTACGGCACACACACACACACACACACACAAATTGCTAGCTACCGT
GATCACTGTTACGGCACACACACACACACACACACACACACAAAATTGCTAGCTACCGT
123
allele
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Current use of Recombinant Inbred Strains
Cartilage and bone changes during development of post-traumatic osteoarthritis in selected LGXSM recombinant inbred mice.Hashimoto S, Rai MF, Janiszak KL, Cheverud JM, Sandell LJ.Osteoarthritis Cartilage. 2012 Feb 8.
The genome architecture of the collaborative cross mouse genetic reference population.Collaborative Cross Consortium.Genetics. 2012 Feb;190(2):389-401.
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Collaborative Cross (CC)
Multiparental recombinant inbred panel derived from eight laboratory mouse inbred strains
Genome architecture analyzed for 350 genetically independent CC lines
Custom genotyping array with 7500 SNPs
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The mouse tilted mutation ✴ tilted (tlt) is a spontaneous recessive mutation in a
C57B6/J background
✴ The tlt/tlt mutant specifically lacks otoconia and consequently does not sense spatial orientation relative to the force of gravity
✴ The tlt defect is highly penetrant
✴ Exhibits no degeneration of the sensory epithelium
✴ Has no apparent abnormal phenotype in other organ systems (Non-syndromic)
✴ The tlt mutation maps to the proximal region of mouse Chr5
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Phenotyping the tilted mouse
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Anatomy and Histology of the Vestibular System
Semi-circular Canals(angular acceleration)
Cochlea (Hearing)
Saccule & Utricle (linearacceleration + gravity)
OtoconiaGelatin layer
Supporting cellHair cell Type IHair cell Type II
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TLTWT
Histopathology of the tlt mouse
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✴ mergulhador (mlh) is a recessive mutation
✴ The mlh/mlh mutant displays non-swimming behavior
✴ mlh/mlh mice lack otoconia but show no other grossmalformations of the inner ear or of any other organ system
✴ mlh maps to the proximal region of mouse Chr 5
Are tilted and mlh two mutant alleles of the same gene?
The mergulhador (diver) mice
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Complementation test:
tlt/tlt x mlh/mlh
Result: tlt/mlh mice do not swim normally
Conclusion: tlt and mlh are allelic
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The tilted locus was originally mapped to mousechromosome 5 by establishing linkage to Hm and Kit.
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Mouse Chr 5
tlt(40 cM)
Hm
Kit
Lane, (1986, 1987)
Hammertoe locus
c-Kit proto-oncogene
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Positional Cloning Strategy
Genetic MappingMIT Markers (non-coding)
Genes (coding)
F2 intercross C57BL/6J- tlt x Mus castaneous (500 mice)
T3 Mouse-Hamster Radiation Hybrid panel (100 cell lines)
Synteny with human
Physical Mapping
Candidate Gene
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Strategy for mapping the tlt locus (T)
G1
parental strains
B6 X M. castaneus (TT) (tt)
....100-500
Save all TT progeny (can’t swim)
X
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Haplotype analysis - intersubspecific crossF2 (C57BL6/J-tlt x M. m. castaneus) x (C57BL6/J-tlt x M. m. castaneus)
tlt
D5Dmo1 BB BC BC BC BC BC BC BC BB BB
D5Mit182 BB BB BC BC BC BC BC BC BB BB
D5Mit421 BB BB BB BC BC BC BC BC BB BB
D5Dmo2 BB BB BB BB BC BC BC BC BB BB
D5Dmo3 BB BB BB BB BB BB BC BC BB BB
D5Dmo4 BB BB BB BB BB BB BB BC BB BB
D5Mit77 BB BB BB BB BB BB BB BC BB BB
D5Mit353 BB BB BB BB BB BB BB BC BC BB
D5Dmo5 BB BB BB BB BB BB BB BC BC BC
D5Dmo6 BB BB BB BB BB BC BB BC BC BC
Total: 487 456 1 2 1 2 1* 3 1 8 12
STS marker Genotype
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Mouse Chr 5
tlt(40 cM)
Hm
Kit
tlt(1.1 cM)
Dmo3D5Mit353
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Genetic Map
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Synteny between Human Chr 4 and Mouse Chr 5
Human Chr 4 Mouse Chr 5
tlt
4p16.3-4p15.1
4p
4q
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Human-Mouse Comparative Mapping of the tlt Locus
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Positional Cloning Strategy
✴ Genetic Mapping
✴ Physical Mapping
Chromosome Walking (BAC clones)
Genomic sequence
✴ Candidate Gene
✓
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Positional Cloning Strategy
✴ Genetic Mapping
✴ Physical Mapping
✴ Candidate Gene
✓
✓
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Preliminary Expression Study 1. Extract RNA from mouse otocyst (E16.5 and P0 stages) 2. Determine the gene expression of 4 candidate genes ( RT-PCR assay)
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Novel gene (26795 bp)
1 kb
Exon Exon length Splice donor Splice acceptor Intron Intron length1?2 407 cggggaccag ACTGG TCGCG gtgagtggcta 2 100723 137 tcccgtccag GAAGC TGCAG gtaaactcct 3 64554 59 ttccatctag GTGTA GAAAG gtaaaaaact 4 33095 131 gctttttcag GTTTG CATCG gtgaggaagc 5 1635
6 908 actgccctag TTTTG TCTCG gtaatcttca 6 2192
7 1490 tctctttcag CTTTG
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Point Mutation --
--
NDND
tlt
mlh--Point Mutation
268D19376E18
115A12426E16
Drd5 Glut9 Wdr1
tlt
Otopetrin KIAA1729
(450 kb)
Otis: EarPetra: Stone
Mutation screening test (sequencing) 1. Draft sequence 4 mouse BACs 2. Determine the gene structure of 4 candidate genes (total of 37 exons)
3. Sequence exons and splice site junctions in tlt mutant
4. Compare with WT sequence
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RP23-426E16: full sequence and annotation
1 50
10051
101 150
151
Lyar
Drd5
Glut9
Otopetrin (Otop)2810021O14RIK
BI697072
195
T7
Sp6
1 2 3 45 678 9 10 1 2
3 4 5 32 4 5 6 7
12 11
78910
tlt mlh
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Mutation Screening of the tlt mutant
C57B6/J +/+
C57B6/J tlt/tlt
T C G CA G C G
T C G AA G C T
TaqI
+/+ tlt/tlt +/tlt
–391bp–230bp–161bp
GSITLFAFITVVLGCLKVAYFIGFSECLSATEGVFPVTHAVHTLLQ GSITLFAFITVVLGCLKVEYFIGFSECLSATEGVFPVTHAVHTLLQ
+/+tlt/tlt
TM
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Mutation Screening of the mlh mutant
542bp481bp
B
+/+mlh/mlh
DLLVATGSGSWLLSWGSILAIACAETRPPYTWYNLPYSVLVIVEKYVQNIFDLLVATGSGSWLLSWGSIQAIACAETRPPYTWYNLPYSVLVIVEKYVQNIF
Balb/c mlh/mlh
Balb/c +/+
T G G C C AA C C G G T
MscI
A
A G G C C AT C C G G T
C
Balb/c mlh/mlh
Balb/c+/ +
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Time line for mouse genetic engineering
Development of chimeras between embryos with different genotypes
Transgenic mice first derived by infecting embryos with retroviruses
First DNA injection into mouse eggs
First embryonic stem cells developed
Germline contribution of ES cells
First genetic modification of an ES cell (HPRT gene)
Improved vectors for homologous recombination
1960s
1974, 1976
1980 1981
1981
1984
1987
1987
Tarkowski, Mintz, Gardner
Jaenisch and Mintz
Gordon, Brinster, Constantini, Lacy, Wagner Martin, Evans, Kaufman
Bradley
Smithies
Thomas and Capecchi.
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Time line for mouse genetic engineering - cont.
Phenotypic consequences of targeted genes
Conditional gene targeting-cre/lox
Conditional gene targeting-flip/FRT
Multiple conditional alleles, cre, flip
Somatic cloning of mice
Lentiviral vectors for transgenesis
RNAi in mice
Sleeping Beauty transposon mutagenesis
Conditional Mouse Knockout Project
Genomic editing
1990+
1992/1993
1996
1998-
1998
2002
2002
2005
2006 -
2010 -
Marth, Rajewsky
Dymecki
Martin
Wakayama et al
Lois, Baltimore
Conklin,Rosenquist
Jenkins,Copeland
EUCOMM, KOMP
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The Nobel Prize in Physiology or Medicine 2007
"for their discoveries of principles for introducing specific gene modifications in mice by the use of embryonic stem cells"
Mario R. Capecchi Sir Martin J. Evans Oliver Smithies
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How do we analyze gene function in mice?
Gene addition (transgenic approach)Permits GOF and DN experimentsEctopic (spatial or temporal) expressionAllows gene regulatory elements to be testedAllows populations of cells to be marked with a reporter gene
Targeted mutationsSpecific genes can be targetedUnexpected phenotypes (lethal phenotype may result prior to the spatial and temporal site of interest)Must be very careful to make a null allele
Tissue-specific targeted mutationsProvides some of the best features of gene targeting and transgenic approachesMay be combined with enhancer trap and gene trap experiments.
Conditional gene targetingAn effective method to circumvent embryonic lethality.