#PAGE_PARAMS# #ADS_HEAD_SCRIPTS# #MICRODATA#

Retrotransposon Activates Ectopic Expression: A Short Tail


article has not abstract


Vyšlo v časopise: Retrotransposon Activates Ectopic Expression: A Short Tail. PLoS Genet 9(2): e32767. doi:10.1371/journal.pgen.1003331
Kategorie: Perspective
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.pgen.1003331

Souhrn

article has not abstract


Zdroje

1. DanforthCH (1925) Hereditary doubling suggesting anomalous chromatin distribution in the mouse. Proc Soc Exp Biol Med 23: 145–147.

2. DanforthCH (1930) Developmental anomalies in a special strain of mice. Am J Anat 45: 275–287.

3. DunnLC, Gluecksohn-SchoenheimerS, BrysonV (1940) A new mutation in the mouse affecting spinal column and urogenital system. J Hered 31: 343–348.

4. MattmanR, ZachgoJ, GosslerA (1997) The Danforth's short tail mutation acts cell autonomously in notochord cells and ventral hindgut endoderm. Development 124: 4019–4028.

5. VlangosCN, SiuniakAN, RobinsonD, ChinnaiyanAM, LyonsRH, et al. (2013) Next generation sequencing identifies the Danforth's short tail mouse mutation as a retrotransposon insertion affecting Ptf1a expression. PLoS Genet 9: e1003205 doi:10.1371/journal.pgen.1003205

6. LuganiF, AroraR, PapetaN, PatelA, ZhengZ, et al. (2013) A retrotransposon insertion in the 5′ regulatory domain of Ptf1a results in ectopic gene expression and multiple congenital defects in Danforth's short tail mouse. PLoS Genet 9: e1003206 doi:10.1371/journal.pgen.1003206

7. SembaK, ArakiK, MatsumotoK, SudaH, AndoT, et al. (2013) Ectopic expression of Ptf1a induces spinal defects, urogenital defects, and anorectal malformations in Danforth's short tail mice. PLoS Genet 9: e1003204 doi:10.1371/journal.pgen.1003204

8. SellickGS, BarkerKT, Stolte-DijkstraI, FleischmannC, ColemanRJ, et al. (2004) Mutations in PTF1A cause pancreatic and cerebellar agenesis. Nat Genet 36: 1301–1305.

9. HoshinoM, NakamuraS, MoriK, KawauchiT, TeraoM, et al. (2005) Ptf1a, a bHLH transcriptional gene, defines GABAergic neuronal fates in cerebellum. Neuron 47: 201–213.

10. GlasgowSM, HenkeRM, MacdonaldRJ, WrightCV, JohnsonJE (2005) Ptf1a determines GABAergic over glutamatergic neuronal cell fate in the spinal cord dorsal horn. Development 132: 5461–5469.

11. AlfredJB, RanceK, TaylorBA, PhillipsSJ, AbbottCM, et al. (1997) Mapping in the region of Danforth's short tail and the localization of tail length modifiers. Genome Res 7: 108–117.

12. HamiltonBA, FrankelWN (2001) Of mice and genome sequence. Cell 107: 13–16.

13. ArakiK, ArakiM, YamamuraK (2002) Site-directed integration of the cre gene mediated by Cre recombinase using a combination of mutant lox sites. Nucleic Acids Res 30: e103.

14. SidowA, BulotskyMS, KerrebrockAW, BirrenBW, AltshulerD, et al. (1999) A novel member of the F-box/WD40 gene family, encoding dactylin, is disrupted in the mouse dactylaplasia mutant. Nat Genet 23: 104–107.

15. KanoH, KurahashiH, TodaT (2007) Genetically regulated epigenetic transcriptional activation of retrotransposon insertion confers mouse dactylaplasia phenotype. Proc Natl Acad Sci U S A 104: 19034–19039.

16. RibetD, DewannieuxM, HeidmannT (2004) An active murine transposon family pair: retrotransposition of “master” MusD copies and ETn trans-mobilization. Genome Res 14: 2261–2267.

17. ZhangY, MaksakovaIA, GagnierL, van de LagemaatLN, MagerDL (2008) Genome-wide assessments reveal extremely high levels of polymorphism of two active families of mouse endogenous retroviral elements. PLoS Genet 4: e1000007 doi:10.1371/journal.pgen.1000007

Štítky
Genetika Reprodukčná medicína

Článok vyšiel v časopise

PLOS Genetics


2013 Číslo 2
Najčítanejšie tento týždeň
Najčítanejšie v tomto čísle
Kurzy

Zvýšte si kvalifikáciu online z pohodlia domova

Aktuální možnosti diagnostiky a léčby litiáz
nový kurz
Autori: MUDr. Tomáš Ürge, PhD.

Všetky kurzy
Prihlásenie
Zabudnuté heslo

Zadajte e-mailovú adresu, s ktorou ste vytvárali účet. Budú Vám na ňu zasielané informácie k nastaveniu nového hesla.

Prihlásenie

Nemáte účet?  Registrujte sa

#ADS_BOTTOM_SCRIPTS#