ライフサイエンスコーパス: multicellularity

1 nd was necessary for the evolution of animal multicellularity.

2 in basic processes associated with metazoan multicellularity.

3 pmental changes relevant to the evolution of multicellularity.

4 not cause potassium leakage failed to induce multicellularity.

5 ve played roles in the evolution of metazoan multicellularity.

6 rst the eukaryotic cell and later eukaryotic multicellularity.

7 ecological context during the transition to multicellularity.

8 ng the evolution of cell differentiation and multicellularity.

9 y have contributed to the advent of metazoan multicellularity.

10 tural novelties in Eukarya perhaps linked to multicellularity.

11 rons and ectopic expression at the origin of multicellularity.

12 for a long time was considered a hallmark of multicellularity.

13 ehavior during the earliest experiments with multicellularity.

14 Xdh gene in eukaryotes, before the origin of multicellularity.

15 ts that they are associated with the rise of multicellularity.

16 one of the early steps in the development of multicellularity.

17 ultrastructure when examining the origins of multicellularity.

18 erefore be an early step in the evolution of multicellularity.

19 e worm may have contributed to the advent of multicellularity.

20 during the initial step in the evolution of multicellularity.

21 s to have had an impact during the origin of multicellularity.

22 ther mechanistic studies on the emergence of multicellularity.

23 ms for understanding the evolution of animal multicellularity.

24 ping clusters may often be the first step to multicellularity.

25 not necessarily alongside, the emergence of multicellularity.

26 e challenges in how to organize and maintain multicellularity.

27 ulatory systems and the evolution of complex multicellularity.

28 organism, and this acts as a gating step for multicellularity.

29 ts, and rarer metazoan innovations linked to multicellularity.

30 key factor underlying the diverse origins of multicellularity.

31 l roles in the generation and maintenance of multicellularity.

32 ich evolved in tandem with the transition to multicellularity.

33 pression is essential for the maintenance of multicellularity.

34 oviding a necessary step in the evolution of multicellularity.

35 ic mechanisms, facilitated the transition to multicellularity.

36 y during the transition from single cells to multicellularity.

37 teria are a beautiful example of prokaryotic multicellularity.

38 select for the evolution of undifferentiated multicellularity.

39 PCD in microbes, including the evolution of multicellularity.

40 s was already in place at the dawn of animal multicellularity.

41 aiming to better understand genomic basis of multicellularity.

42 atterns as genomic and evolutionary basis of multicellularity.

43 cine algae coevolved with the acquisition of multicellularity.

44 ve demarcated the genetic toolkit for animal multicellularity, a select set of a few hundred genes fr

45 emical, and mechanistic basis of prokaryotic multicellularity, a topic that has garnered considerable

46 ment, expression pattern diversification and multicellularity, aiming to better understand genomic ba

47 Coming together amplifies the benefits of multicellularity and allows social clusters to collectiv

48 Volvox, a model system for the evolution of multicellularity and cellular differentiation.

49 entally responsive molecular determinants of multicellularity and contribute to the natural morpholog

50 ework for investigating the origin of animal multicellularity and development.

51 ed for the investigation of the evolution of multicellularity and development.

52 veal the importance of TFs to the origins of multicellularity and embryonic development.

53 including the emergence of eukaryotic cells, multicellularity and eusociality.

54 and facilitating evolutionary transitions to multicellularity and germ-soma differentiation in the vo

55 he major evolutionary transition to obligate multicellularity and had more cell types, a higher likel

56 al control mechanism governing the switch to multicellularity and raises the possibility that YlbF, Y

57 cadherins, which are essential for metazoan multicellularity and restricted to metazoans and their c

58 at differ only in the presence or absence of multicellularity and somatic differentiation, permitting

59 ion of orthologs of genes known to establish multicellularity and tissue architecture in metazoans.

60 to the understanding of natural evolution of multicellularity and to manipulating cell sedimentation

61 ordinated expression of strongly interacting multicellularity and unicellularity processes was lost i

62 complex RNA-silencing systems evolved before multicellularity and were a feature of primitive eukaryo

63 ation, the evolution of the eukaryotic cell, multicellularity, and the origin of human groups with la

64 s, the Palmophyllales, with a unique form of multicellularity, and typically found in deep water.

65 ful independent solutions to the problems of multicellularity - animals and higher plants.

66 Multicellularity appeared early and repeatedly in life's

67 Evolution of multicellularity appears to have been accompanied by a s

68 of living myocardium that retain the native multicellularity, architecture and physiology of the hea

69 nges that ultimately led to the evolution of multicellularity are not known.

70 lular relatives indicate that transitions to multicellularity are typically associated with increases

71 Multicellularity arose as a result of adaptive advantage

72 d of modular domains have evolved along with multicellularity as a method to facilitate increasing in

73 ns must be key players in the development of multicellularity because they are well positioned to for

74 nscription factors are key players in animal multicellularity, being members of the T-box family that

75 verge to control complex processes including multicellularity, biofilm formation, and virulence.

76 Integrin-mediated adhesion is as ancient as multicellularity, but it was not always as complex as it

77 tions have been identified in the context of multicellularity, but they have been treated very simila

78 gg, the social amoeba Dictyostelium achieves multicellularity by the aggregation of approximately 10(

79 With increasing specialization and multicellularity, C3 evolved a secretory capacity that a

80 We argue that multicellularity can prevent the victory of such mutants

81 ife histories, including social behavior and multicellularity, can only be understood in the appropri

82 The advent of complex multicellularity (CM) was a pivotal event in the evoluti

83 has been to understand how the evolution of multicellularity conferred fitness advantages.

84 lar, soma-producing strains, suggesting that multicellularity confers evolutionary stability to somat

85 In this way, multicellularity could have originated.

86 These results suggest that multicellularity could have played a key role in trigger

87 nities do not satisfy the strict criteria of multicellularity developed by multi-level selection theo

88 Here it is suggested that multicellularity discourages selection against weak muta

89 and possible interplay between the origin of multicellularity, diversification of cyanobacteria, and

90 The evolution of multicellularity enabled specialization of cells, but re

91 The transition to multicellularity enabled the evolution of large, complex

92 ism has become a model for understanding how multicellularity evolved in the animal lineage.

93 We do not know how or why multicellularity evolved.

94 The primitive 'multicellularity' exhibited by certain cellulolytic micr

95 genes and their corresponding tRNAs, and in multicellularity genes and their tRNAs, suggesting the e

96 s enriched among the cell-autonomous and the multicellularity genes, respectively.

97 ot in laboratory strains, an indication that multicellularity has been lost during domestication of B

98 iridiplantae comprise unicellular algae, and multicellularity has evolved independently in the two cl

99 Multicellularity has evolved multiple times, but animals

100 The transition to multicellularity has occurred numerous times in all doma

101 Studies on the origin of animal multicellularity have increasingly focused on one of the

102 l amoebas (Dictyostelia) display conditional multicellularity in a wide variety of forms.

103 The evolution of multicellularity in animals required the production of e

104 mergence of BMs coincided with the origin of multicellularity in animals, suggesting that they were e

105 ernal" transitions, such as the evolution of multicellularity in animals.

106 ria might also have influenced the origin of multicellularity in animals.

107 ibed quorum-sensing mechanism for triggering multicellularity in Bacillus subtilis.

108 osetta as a model system for studying simple multicellularity in choanoflagellates and provide an exp

109 s of the developmental pathway that leads to multicellularity in Dictyostelium.

110 nd how they have adapted to the emergence of multicellularity in eukaryotes.

111 genes may have some relation to the rise of multicellularity in green plants.

112 en suggested that they evolved together with multicellularity in separate plant and animal lineages.

113 h a comparative study, comparing the form of multicellularity in species where groups are clonal (r =

114 (+)], governs the acquisition of facultative multicellularity in the budding yeast Saccharomyces cere

115 l resource in understanding the evolution of multicellularity in the fungi.

116 Among the best-studied ETIs is the origin of multicellularity in the green alga Volvox, a model syste

117 ystem for understanding the genetic basis of multicellularity including the initial formation of coop

118 ants and animals are thought to have evolved multicellularity independently.

119 Multicellularity inherently involves a number of coopera

120 The transition to multicellularity is a key feature of the Dictyostelium l

121 llularity overlaps with the GOE, and whether multicellularity is associated with significant shifts i

122 An obvious requirement for successful multicellularity is communication between different part

123 Together, these data show that rudimentary multicellularity is deeply rooted in the Ascomycota.

124 Their complex multicellularity is inconsistent with a phylogenetic aff

125 Amongst eukaryotes, this form of multicellularity is mainly studied in the social amoeba

126 This ability to shift between uni- and multicellularity makes the group ideal for studying the

127 y and frequently, the selective advantage of multicellularity may be large.

128 s, the organizational principles of metazoan multicellularity may be more ancient than previously rec

129 The origin of animal multicellularity may be reconstructed by comparing anima

130 elated to halogen metabolism, oxylipins, and multicellularity (microRNA processing and transcription

131 l-autonomous functions and genes involved in multicellularity obey distinct codon usage.

132 n ccs52A1 mutations dramatically enhance the multicellularity of sim mutants trichomes in double muta

133 s harbor features important in sexuality and multicellularity once believed to have originated in met

134 ransitions can be recursive (e.g., plastids, multicellularity) or limited (transitions that share the

135 We tested whether the evolution of multicellularity overlaps with the GOE, and whether mult

136 peration and competition for the benefits of multicellularity promote the stable coexistence of unice

137 ll biology, we reason that the transition to multicellularity required modification of pre-existing m

138 The evolution of multicellularity required novel mechanisms for intercell

139 We conclude that the transition to multicellularity required novel signals and sensors rath

140 Aggregative multicellularity, resulting in formation of a spore-bear

141 omonas reinhardtii to conditions that favour multicellularity, resulting in the evolution of a multic

142 The independent instances of multicellularity reviewed indicate that advantages in fe

143 may constitute a barrier to the evolution of multicellularity since cell differentiation requires sen

144 ty that likely relate to the requirements of multicellularity such as the need to establish faithful

145 tonomous timing allows a trial commitment to multicellularity that external signals could extend.

146 The transition to multicellularity that launched the evolution of animals

147 early and formative step in the evolution of multicellularity, the evolution of cell cycle regulation

148 However, as the transition proceeds to multicellularity, the group level trade-offs depart from

149 isiae to an environment in which we expected multicellularity to be adaptive.

150 mechanisms evolved during the transition to multicellularity to control fundamental cellular process

151 to diverse biological phenomena ranging from multicellularity to mutualism.

152 Here we report the evolution of multicellularity via two distinct mechanisms of group fo

153 in normal tissues, the evolution of complex multicellularity was not accompanied by reductions in mu

154 Multicellularity was one of the most significant innovat

155 Small-molecule-induced multicellularity was prevented by the addition of potass

156 It has been a decade since multicellularity was proposed as a general bacterial tra

157 hanisms underlying the evolution of metazoan multicellularity, we sequenced and analysed the genome o

158 , reproductive division of labor, and clonal multicellularity while maintaining sufficient generality

159 g between cells accompanies the evolution of multicellularity with cell differentiation.