ライフサイエンスコーパス: mitochondrial inheritance

1 itochondrial partitioning into growing buds (mitochondrial inheritance).

2 ernal inheritance, a pattern consistent with mitochondrial inheritance.

3 r mutant (mmr1Delta gem1Delta) with impaired mitochondrial inheritance.

4 hat GEM1, MMR1, and YPT11 each contribute to mitochondrial inheritance.

5 e most consistent with a biparental model of mitochondrial inheritance.

6 e maternal lineage with a pattern indicating mitochondrial inheritance.

7 ty of Rsp5p is essential for its function in mitochondrial inheritance.

8 which are suppressed by artificially forcing mitochondrial inheritance.

9 ugh the HOG pathway to control the timing of mitochondrial inheritance.

10 er generation" rule and three other rules of mitochondrial inheritance.

11 for rare early-onset forms with monogenic or mitochondrial inheritance.

12 sociation is essential for Ypt11 function in mitochondrial inheritance.

13 features of Ypt11 function and regulation in mitochondrial inheritance.

14 iparental disomy, unusual characteristics of mitochondrial inheritance also have been found that defy

15 Ypt11, bind Myo2 and have been implicated in mitochondrial inheritance, although their specific roles

16 tion of a yeast mutant, mdm20, in which both mitochondrial inheritance and actin cables (bundles of a

17 cking MDM20 function display defects in both mitochondrial inheritance and actin organization, specif

18 usly implicated in endoplasmic reticulum and mitochondrial inheritance and for a COPI coatomer subuni

19 nfiltration of this mistake into concepts of mitochondrial inheritance and human evolution.

20 e first evidence of a role for prohibitin in mitochondrial inheritance and in the regulation of mitoc

21 ay temperature-sensitive growth and aberrant mitochondrial inheritance and morphology at the nonpermi

22 These results indicate that Mgm1p is a mitochondrial inheritance and morphology component that

23 ith an mgm1-null mutation displayed aberrant mitochondrial inheritance and morphology.

24 tin cables, mutations in these genes disrupt mitochondrial inheritance and nuclear segregation to dif

25 sses, including secretory vesicle transport, mitochondrial inheritance, and nuclear orientation.

26 mediated by Rsp5p plays an essential role in mitochondrial inheritance, and reveal a novel function f

27 In the case of mitochondrial inheritance, anterograde movement drives t

28 Thus quantity and quality of mitochondrial inheritance are ensured by two opposing pr

29 tin-dependent force generators contribute to mitochondrial inheritance: Arp2/3 complex and the myosin

30 findings indicate that Mmr1p contributes to mitochondrial inheritance as a mediator of anchorage of

31 ission; Class II alleles displayed defective mitochondrial inheritance but had no effect on nuclear m

32 atase, has previously been shown to regulate mitochondrial inheritance by an unknown mechanism.

33 lta double mutants correlated with defective mitochondrial inheritance by large buds.

34 licative segregation, and threshold effects, mitochondrial inheritance can allow for the apparent spo

35 mitochondrial nucleoid, the genetic unit of mitochondrial inheritance, can contain a single copy of

36 showing no evidence of a proposed cell-cycle mitochondrial inheritance checkpoint.

37 hen combined with a mutation in any of three mitochondrial inheritance components of the mitochondria

38 cue temperature-sensitive growth defects and mitochondrial inheritance defects and partially restore

39 lament-binding protein tropomyosin, suppress mitochondrial inheritance defects and partially restore

40 The mitochondrial inheritance delay in the ptc1 mutant is no

41 lly controlled and provide new evidence that mitochondrial inheritance does not depend on a physical

42 restrictive temperature, cells defective in mitochondrial inheritance give rise to dead buds that go

43 As a result, much of what we know regarding mitochondrial inheritance has been uncovered using yeast

44 ant inactivation of Slt2p is also needed for mitochondrial inheritance; however, in this case, the re

45 hibits cytokinesis in response to defects in mitochondrial inheritance in budding yeast.

46 have been identified as the genetic units of mitochondrial inheritance in yeast and man, little is kn

47 emonstrates that multiple pathways influence mitochondrial inheritance in yeast and that Miro GTPases

48 ese results provide compelling evidence that mitochondrial inheritance in yeast is an actin-mediated

49 Proteins reported to influence mitochondrial inheritance include the mitochondrial rho

50 Thus, active mitochondrial inheritance is an essential process and a

51 Mitochondrial inheritance is essential for cell division

52 When mitochondrial inheritance is inhibited, Num1 clusters ar

53 We show that yeast mitochondrial inheritance is not required for inheritanc

54 Mitochondrial inheritance is tightly coupled with bud em

55 ence of sex chromosomes, obligate sexuality, mitochondrial inheritance linked to the mating type, and

56 tion causes temperature-dependent defects in mitochondrial inheritance, mitochondrial morphology, and

57 In wild-type yeast mitochondrial inheritance occurs early in the cell cycle

58 have a specific and severe defect in active mitochondrial inheritance, revealing mitochondrial trans

59 c pair was used to investigate three traits: mitochondrial inheritance, the effect of the MAT alleles

60 Mitochondrial inheritance, the transfer of mitochondria

61 Inhibiting mitochondrial inheritance to buds, by deletion of MMR1,

62 uggesting a role for both Num1p and Dnm1p in mitochondrial inheritance, we find that num1 dnm1 double