Download presentation
Presentation is loading. Please wait.
1
Janet Berrios March 19, 2009 http://sgc.utoronto.ca/SGC-WebPages/StructureDescription/img/2V1X_400x400.png
2
Extremely rare ~220 cases since 1975 Usually of Ashkenazi Jewish origin Autosomal Recessive Cancer Diagnosis at 24, Death before 30 Characteristics: Slow Growth Proportional Dwarfism Beaked nose, narrow face, prominent ears High pitched voice Pigmentation, redness, and dilated blood vessels in skin Mental retardation Diabetes (Type II) Immune Deficiency Lung Problems Low or no fertility Malignancies: early onset; particularly non-Hodgkin’s lymphoma, leukemias and carcinomas of the breast, gut and skin V.A. Bohr Cell Press Review, 2008; I.D. Hickson Nature Reviews – Cancer, 2003 http://www.bio.davidson.edu/Courses/ Molbio/MolStudents/spring2003/Baxter /BLM.gif
3
I.D. Hickson, Nature Reviews -- Cancer 2003
4
A tumor-suppressor Chromosome 15 Regulated by phosphorylation I.D. Hickson, Nature Reviews -- Cancer 2003
5
Premature Aging Bilateral Cataracts Hoarseness Skin Alterations Thin Limbs Premature graying, Alopecia Short Stature Osteoporosis Hypogonadism Diabetes (Type II) Soft Tissue Calcification Loss of Subcutaneous Fat Malignancies: early onset; primarily sarcomas and mesenchymal tumors, some melanoma and thyroid cancers V.A. Bohr Cell Press Review, 2008; I.D. Hickson Nature Reviews – Cancer, 2003 http://www.scripps.edu/~jjperry/research.html
6
C.Z. Bacharati, I.D. Hickson. Chormosoma - Review (2008) http://www.nature.com/ncb/journal/v6/n3/images/ncb0304-184a-i1.jpg Holliday Junction G-quadruplex
7
First thought to be lethal BLM deficient mice have: Cancers of different cellular origins But... Lack other Bloom’s syndrome characteristics What about heterozygotes? Haploinsufficiency? Needed Loss of Heterozygosity? Predisposition to cancers? BLM +/- mice did have enhanced tumor formation indicating haploinsufficiency
8
Two main mutation features: Founder effects Full range of mutation types which impairs protein expression Nature Reviews - Cancer, 2003 BLM ASH
9
Highly conserved throughout evolution Bloom’s syndrome is autosomal recessive BLM is an ATP-dependent helicase that works in a 3’ 5’ direction that affects genomic stability BLM is active at replication sites where the replication fork has arrested Many different mutations can occur but all impair protein expression Biallelic mutation is only correlative to cancer
Similar presentations
© 2025 SlidePlayer.com. Inc.
All rights reserved.