Редактирование: BTD

Biotinidase precursor (EC 3.5.1.12) (Biotinase)

==Publications==

{{medline-entry
|title=A test of independence of discounting from quality of life.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/22277284
|abstract=The quality-adjusted life-years (QALY) model assumes quality and quantity of life can be multiplied into a single index and requires quality and quantity to be mutually independent, which need not hold empirically. This paper proposes a new test for measuring independence of utility of life duration from quality of life in a riskless setting. We use a large representative sample of Dutch citizens and include two health states generally considered better than dead ([[BTD]]) and one health state considered worse than dead (WTD). Independence cannot be rejected when comparing the [[BTD]] health states, but is rejected when comparing the [[BTD]] states with the WTD state. In particular, utility of life duration becomes more concave for the WTD state. This may suggest that independence holds only for [[BTD]] health states. This has implications for the QALY model and would require using sign-dependent utility of life duration functions.
|mesh-terms=* Health Status
* Humans
* Longevity
* Models, Econometric
* Netherlands
* Quality of Life
* Quality-Adjusted Life Years
* Time Factors

|full-text-url=https://sci-hub.do/10.1016/j.jhealeco.2011.12.001
}}
{{medline-entry
|title=Drosophila melanogaster holocarboxylase synthetase is a chromosomal protein required for normal histone biotinylation, gene transcription patterns, lifespan, and heat tolerance.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/17056793
|abstract=Post-translational modifications of histones play important roles in chromatin structure and genomic stability. Distinct lysine residues in histones are targets for covalent binding of biotin, catalyzed by holocarboxylase synthetase (HCS) and biotinidase ([[BTD]]). Histone biotinylation has been implicated in heterochromatin structures, DNA repair, and mitotic chromosome condensation. To test whether HCS and [[BTD]] deficiency alters histone biotinylation and to characterize phenotypes associated with HCS and [[BTD]] deficiency, HCS- and [[BTD]]-deficient flies were generated by RNA interference (RNAi). Expression of HCS and [[BTD]] decreased by 65-90% in RNAi-treated flies, as judged by mRNA abundance, [[BTD]] activity, and abundance of HCS protein. Decreased expression of HCS and [[BTD]] caused decreased biotinylation of K9 and K18 in histone H3. This was associated with altered expression of 201 genes in HCS-deficient flies. Lifespan of HCS- and [[BTD]]-deficient flies decreased by up to 32% compared to wild-type controls. Heat tolerance decreased by up to 55% in HCS-deficient flies compared to controls, as judged by survival times; effects of [[BTD]] deficiency were minor. Consistent with this observation, HCS deficiency was associated with altered expression of 285 heat-responsive genes. HCS and [[BTD]] deficiency did not affect cold tolerance, suggesting stress-specific effects of chromatin remodeling by histone biotinylation. To our knowledge, this is the first study to provide evidence that HCS-dependent histone biotinylation affects gene function and phenotype, suggesting that the complex phenotypes of HCS- and [[BTD]]-deficiency disorders may reflect chromatin structure changes.
|mesh-terms=* Animals
* Biotinidase
* Biotinylation
* Carbon-Nitrogen Ligases
* Chromosomal Proteins, Non-Histone
* Drosophila melanogaster
* Gene Expression Profiling
* Histones
* Hot Temperature
* Life Expectancy
* RNA Interference
* Transcription, Genetic

|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1626655
}}