Erratum to: Mosaic variegated aneuploidy in mouse BubR1 deficient embryos and pregnancy loss in human [Chromosome Research, 10.1007/s10577-014-9432-x];Mosaic variegated aneuploidy in mouse BubR1 deficient embryos and pregnancy loss in human

Chromosome Research

Volumn 22, Issue 3, 2014, Pages 375-392

  Schmid, Michael ^a   Steinlein, Claus ^a   Tian, Qi ^b   Hanlon Newell, Amy E ^b   Gessler, Manfred ^c   Olson, Susan B ^b   Rosenwald, Andreas ^a   Kneitz, Burkhard ^a   Fedorov, Lev M ^a,b  

^a UNIVERSITY OF WÜRZBURG   (Germany)

^b OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

^c UNIVERSITY OF WÜRZBURG   (Germany)

Author keywords

BubR1 deficiency; Mosaic variegated aneuploidy; Pregnancy loss; Spindle assembly checkpoint

Indexed keywords

BUB1 RELATED PROTEIN; BUB1B PROTEIN, MOUSE; CELL CYCLE PROTEIN; PROTEIN SERINE THREONINE KINASE;

ADULT; ANEUPLOIDY; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; APOPTOSIS; ARTICLE; CELL DEATH; CELL PROLIFERATION; CHROMOSOME G BAND; CONTROLLED STUDY; EMBRYO; EMBRYO DEATH; EMBRYO DEVELOPMENT; FLUORESCENCE IN SITU HYBRIDIZATION; GENE MUTATION; GENE TARGETING; GENOMIC INSTABILITY; GENOTYPE; GROWTH RETARDATION; HAPLOINSUFFICIENCY; HUMAN; IN VITRO STUDY; INFANT; KARYOTYPE; M PHASE CELL CYCLE CHECKPOINT; METAPHASE; MOSAIC VARIEGATED ANEUPLOIDY; MOSAICISM; MOUSE; NIDATION; NONHUMAN; PHENOTYPE; PREGNANCY TERMINATION; PRIORITY JOURNAL; RECURRENT PREGNANCY LOSS; SISTER CHROMATID; SPECTRAL KARYOTYPING; ANIMAL; ANIMAL EMBRYO; C57BL MOUSE; CHROMOSOME BANDING PATTERN; CONGENITAL MALFORMATION; DEFICIENCY; EMBRYOLOGY; FEMALE; GENETICS; KNOCKOUT MOUSE; METABOLISM; MITOSIS; PATHOLOGY; PREGNANCY;

MUS;

ANEUPLOIDY; ANIMALS; CELL CYCLE PROTEINS; CHROMOSOME BANDING; EMBRYO LOSS; EMBRYO, MAMMALIAN; FEMALE; GENE TARGETING; HAPLOINSUFFICIENCY; HUMANS; MICE, INBRED C57BL; MICE, KNOCKOUT; MITOSIS; MOSAICISM; PHENOTYPE; PREGNANCY; PROTEIN-SERINE-THREONINE KINASES; SPECTRAL KARYOTYPING;

EID: 84906066935     PISSN: 09673849     EISSN: 15736849     Source Type: Journal    
DOI: 10.1007/s10577-014-9441-9     Document Type: Erratum

References (62)

1. Angell RR, Aitken RJ, van Look PF et al (1983) Chromosome abnormalities in human embryos after in vitro fertilization. Nature 303:336-338 (Pubitemid 13081907)
2. Baker DJ, Jeganathan KB, Cameron JD et al (2004) BubR1 insufficiency causes early onset of aging-associated phenotypes and infertility in mice. Nat Genet 36:744-749 (Pubitemid 38886637)
3. Baranov VS, Dyban AP, Chebotar NA (1980) Preimplantation development of mouse embryos with monosomy of autosome No. 17. Ontogenez 11:148-159 (Pubitemid 10118770)
4. Bishop CE, Boursot PB, Baron F et al (1985) Most classical Mus musculus domesticus laboratory mouse strains carry a Mus musculus musculus Y chromosome. Nature 315:70-72 (Pubitemid 15064903)
5. Boue J, Bou A, Lazar P (1975) Retrospective and prospective epidemiological studies of 1500 karyotyped spontaneous human abortions. Teratology 12:11-26
6. Bowen P, Lee CS (1969) Spontaneous abortion. Chromosome studies on 41 cases and an analysis of maternal age and duration of pregnancy in relation to karyotype. Am J Obstet Gynecol 104:973-983
7. Braude P, Bolton V, Moore S (1988) Human gene expression first occurs between the four- and eight-cell stages of preimplantation development. Nature 332:459-461 (Pubitemid 18090251)
8. Burds AA, Lutum AS, Sorger PK (2005) Generating chromosome instability through the simultaneous deletion of Mad2 and p53. Proc Natl Acad Sci U S A 102:11296-11301 (Pubitemid 41153814)
9. Chen CP, Lee CC, Chen WL et al (2004) Prenatal diagnosis of premature centromere division-related mosaic variegated aneuploidy. Prenat Diagn 24:19-25
10. Chin CF, Yeong FM (2010) Safeguarding entry into mitosis: the antephase checkpoint. Mol Cell Biol 30:22-32
11. Cleveland DW, Mao YK, Sullivan F (2003) Centromeres and kinetochores: from epigenetics to mitotic checkpoint signaling. Cell 112:407-421 (Pubitemid 36263076)
12. Coonen E, Harper JC, Ramaekers FC et al (1994) Presence of chromosomal mosaicism in abnormal preimplantation embryos detected by fluorescence in situ hybridisation. Hum Genet 94:609-615 (Pubitemid 24351516)
13. Dai W, Wang Q, Liu T et al (2004) Slippage of mitotic arrest and enhanced tumor development in mice with BubR1 haploinsufficiency. Cancer Res 64:440-445 (Pubitemid 38120879)
14. Daphnis DD, Fragouli E, Economou K et al (2008) Analysis of the evolution of chromosome abnormalities in human embryos from Day 3 to 5 using CGH and FISH. Mol Hum Reprod 14:117-125 (Pubitemid 351321172)
15. de Bruin RA, Wittenberg C (2009) All eukaryotes: before turning off G1-S transcription, please check your DNA. Cell Cycle 8:214-217
16. Dobles M, Liberal V, Scott ML et al (2000) Chromosome missegregation and apoptosis in mice lacking the mitotic checkpoint protein Mad2. Cell 101:635-645
17. Eiben B, Bartels I, Bahr-Porsch S et al (1990) Cytogenetic analysis of 750 spontaneous abortions with the direct-preparation method of chorionic villi and its implications for studying genetic causes of pregnancy wastage. Am J Hum Genet 47:656-663
18. Epstein CJ, Travis B (1979) Preimplantation lethality of monosomy for mouse chromosome 19. Nature 280:144-145 (Pubitemid 9221738)
19. Evsikov S, Verlinsky Y (1998) Mosaicism in the inner cell mass of human blastocysts. Hum Reprod 13:3151-3155 (Pubitemid 28521867)
20. Garcia-Castillo H, Vasquez-Velasquez AI, Rivera H et al (2008) Clinical and genetic heterogeneity in patients with mosaic variegated aneuploidy: delineation of clinical subtypes. Am J Med Genet A 146A:1687-1695 (Pubitemid 351975479)
21. Grande M, Borrell A, Garcia-Posada R et al (2012) The effect of maternal age on chromosomal anomaly rate and spectrum in recurrent miscarriage. Hum Reprod 27:3109-3117
22. Gropp A (1982) Value of an animal model for trisomy. Virchows Arch A Pathol Anat Histol 395:117-131 (Pubitemid 12100698)
23. Gropp A, Kolbus U, Giers D (1975) Systematic approach to the study of trisomy in the mouse. II. Cytogenet Cell Genet 14:42-62
24. Guttenbach M, Steinlein C, Engel W et al (2001) Cytogenetic characterization of the TM4 mouse Sertoli cell line. I. Conventional banding techniques, FISH and SKY. Cytogenet Cell Genet 94:71-78 (Pubitemid 33036047)
25. Handyside AH, Xu K (2012) Preimplantation genetic diagnosis comes of age. Semin Reprod Med 30:255-258
26. Hanks S, Coleman K, Reid S et al (2004) Constitutional aneuploidy and cancer predisposition caused by biallelic mutations in BUB1B. Nat Genet 36:1159-1161 (Pubitemid 41288963)
27. Harper JC, Coonen E, Handyside AH et al (1995) Mosaicism of autosomes and sex chromosomes in morphologically normal, monospermic preimplantation human embryos. Prenat Diagn 15:41-49
28. Hassold T, Chen N, Funkhouser J et al (1980) A cytogenetic study of 1000 spontaneous abortions. Ann Hum Genet 44:151-178 (Pubitemid 11215107)
29. Hodes-Wertz B, Grifo J, Ghadir S et al (2012) Idiopathic recurrent miscarriage is caused mostly by aneuploid embryos. Fertil Steril 98:675-680
30. Ioffe E, Liu Y, Bhaumik M et al (1995) WW6: an embryonic stem cell line with an inert genetic marker that can be traced in chimeras. Proc Natl Acad Sci U S A 92:7357-7361
31. Jeganathan K, Malureanu L, Baker DJ et al (2007) Bub1 mediates cell death in response to chromosome missegregation and acts to suppress spontaneous tumorigenesis. J Cell Biol 179:255-267 (Pubitemid 350004890)
32. Karess RE, Wassmann K, Rahmani Z (2013) New insights into the role of BubR1 in mitosis and beyond. Int Rev Cell Mol Biol 306:223-273
33. Katsumata M, Lo CW (1988) Organization of chromosomes in the mouse nucleus: analysis by in situ hybridization. J Cell Sci 90(Pt 2):193-199
34. Kneitz B, Cohen PE, Avdievich E et al (2000) MutS homolog 4 localization to meiotic chromosomes is required for chromosome pairing during meiosis in male and female mice. Genes Dev 14:1085-1097 (Pubitemid 30324422)
35. Koot YE, Boomsma CM, Eijkemans MJ et al (2011) Recurrent pre-clinical pregnancy loss is unlikely to be a 'cause' of unexplained infertility. Hum Reprod 26:2636-2641
36. Lebedev IN, Ostroverkhova NV, Nikitina TV et al (2004) Features of chromosomal abnormalities in spontaneous abortion cell culture failures detected by interphase FISH analysis. Eur J Hum Genet 12:513-520 (Pubitemid 39077158)
37. Lobrich M, Jeggo PA (2007) The impact of a negligent G2/M checkpoint on genomic instability and cancer induction. Nat Rev Cancer 7:861-869 (Pubitemid 350006255)
38. Macklon NS, Geraedts JP, Fauser BC (2002) Conception to ongoing pregnancy: the 'black box' of early pregnancy loss. Hum Reprod Update 8:333-343 (Pubitemid 34919248)
39. Mantzouratou A, Delhanty JD (2011) Aneuploidy in the human cleavage stage embryo. Cytogenet Genome Res 133:141-148
40. Marquard K, Westphal LM, Milki AA et al (2010) Etiology of recurrent pregnancy loss in women over the age of 35 years. Fertil Steril 94:1473-1477
41. Matsuura S, Matsumoto Y, Morishima K et al (2006) Monoallelic BUB1B mutations and defective mitotic-spindle checkpoint in seven families with premature chromatid separation (PCS) syndrome. Am J Med Genet A 140:358-367 (Pubitemid 43227649)
42. Menasha J, Levy B, Hirschhorn K et al (2005) Incidence and spectrum of chromosome abnormalities in spontaneous abortions: new insights from a 12-year study. Genet Med 7:251-263 (Pubitemid 40638071)
43. Mertzanidou A, Wilton L, Cheng J et al (2013) Microarray analysis reveals abnormal chromosomal complements in over 70% of 14 normally developing human embryos. Hum Reprod 28:256-264
44. Michel LS, Liberal V, Chatterjee A et al (2001) MAD2 haplo-insufficiency causes premature anaphase and chromosome instability in mammalian cells. Nature 409:355-359 (Pubitemid 32151241)
45. Munne S, Grifo J, Cohen J et al (1994) Chromosome abnormalities in human arrested preimplantation embryos: a multiple-probe FISH study. Am J Hum Genet 55:150-159 (Pubitemid 24242395)
46. Musacchio A, Salmon ED (2007) The spindle-assembly checkpoint in space and time. Nat Rev Mol Cell Biol 8:379-393 (Pubitemid 46643240)
47. Park I, Lee HO, Choi E et al (2013) Loss of BubR1 acetylation causes defects in spindle assembly checkpoint signaling and promotes tumor formation. J Cell Biol 202:295-309
48. Plaja A, Vendrell T, Smeets D et al (2001) Variegated aneuploidy related to premature centromere division (PCD) is expressed in vivo and is a cancer-prone disease. Am J Med Genet 98:216-223 (Pubitemid 32118984)
49. Plaja A, Mediano C, Cano L et al (2003) Prenatal diagnosis of a rare chromosomal instability syndrome: variegated aneuploidy related to premature centromere division (PCD). Am J Med Genet A 117A:85-86 (Pubitemid 37059327)
50. Santos MA, Teklenburg G, Macklon NS et al (2010) The fate of the mosaic embryo: chromosomal constitution and development of Day 4, 5 and 8 human embryos. Hum Reprod 25:1916-1926
51. Siegel JJ, Amon A (2012) New insights into the troubles of aneuploidy. Annu Rev Cell Dev Biol 28:189-214
52. Snape K, Hanks S, Ruark E et al (2011) Mutations in CEP57 cause mosaic variegated aneuploidy syndrome. Nat Genet 43:527-529
53. Suijkerbuijk SJ, van Dam TJ, Karagöz GE et al (2012) The vertebrate mitotic checkpoint protein BUBR1 is an unusual pseudokinase. Dev Cell 22(6):1321-1329
54. Tian Q, Hanlon Newell AE, Wang Y et al (2011) Complex cytogenetic analysis of early lethality mouse embryos. Chromosome Res 19:567-574
55. van Echten-Arends J, Mastenbroek S, Sikkema-Raddatz B et al (2011) Chromosomal mosaicism in human preimplantation embryos: a systematic review. Hum Reprod Update 17:620-627
56. Vanneste E, Voet T, Caignec CLE et al (2009) Chromosome instability is common in human cleavage-stage embryos. Nat Med 15:577-583
57. Vleugel M, Hoogendoorn E, Snel B et al (2012) Evolution and function of the mitotic checkpoint. Dev Cell 23:239-250
58. Vorsanova SG, Kolotii AD, Iourov IY et al (2005) Evidence for high frequency of chromosomal mosaicism in spontaneous abortions revealed by interphase FISH analysis. J Histochem Cytochem 53:375-380 (Pubitemid 40344079)
59. Wang Q, Liu T, Fang Y et al (2004) BUBR1 deficiency results in abnormal megakaryopoiesis. Blood 103:1278-1285 (Pubitemid 38168638)
60. Warburton D, Anyane-Yeboa K, Taterka P et al (1991) Mosaic variegated aneuploidy with microcephaly: a new human mitotic mutant? Ann Genet 34:287-292
61. White BJ, Tjio JH, Van de Water LC et al (1974) Trisomy 19 in the laboratory mouse. I. Frequency in different crosses at specific developmental stages and relationship of trisomy to cleft palate. Cytogenet Cell Genet 13:217-231
62. Wijshake T, Malureanu LA, Baker DJ et al (2012) Reduced life- and healthspan in mice carrying a mono-allelic BubR1 MVA mutation. PLoS Genet 8:e1003138