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1  ATU gene at the homologous locus in the new macronucleus.
2 n, which produces a transcriptionally active macronucleus.
3 only wild-type genes in the polycopy somatic macronucleus.
4 nucleus and during anlagen formation for the macronucleus.
5 ot completely, eliminated from the polyploid macronucleus.
6 sion of the gene during development of a new macronucleus.
7  cell: a germline micronucleus and a somatic macronucleus.
8 on of polytene chromosomes in the developing macronucleus.
9 eemingly associated with the position of the macronucleus.
10 omial feeding apparatus and a large C-shaped macronucleus.
11 s into a germline micronucleus and a somatic macronucleus.
12 s to eliminate DNA not wanted in the somatic macronucleus.
13 ion of the germline micronucleus and somatic macronucleus.
14 ninterrupted coding sequences in its somatic macronucleus.
15 age in the mitotic micronucleus and amitotic macronucleus.
16 clei: a germ line micronucleus and a somatic macronucleus.
17  and division of the Tetrahymena thermophila macronucleus.
18  mitotic micronucleus and polyploid amitotic macronucleus.
19 s of the 1.8 kb H1 Indel are retained in the macronucleus.
20 the creation of the transcriptionally active macronucleus.
21 ated subunit, p69, from the cytoplasm to the macronucleus.
22 and is located exclusively in the developing macronucleus.
23 ated cells and is absent from the vegetative macronucleus.
24 e efficiently eliminated from the developing macronucleus.
25 ngement during the formation of a functional macronucleus.
26 he formation of the transcriptionally active macronucleus.
27 cesses occur concomitantly in the developing macronucleus.
28 e represented at an average of 45 copies per macronucleus.
29  electron-dense structures in the developing macronucleus.
30  on chromosome 1L that are also found in the macronucleus.
31  those of the Tec elements in the developing macronucleus.
32 ar genome into the somatic genome of the new macronucleus.
33 ring formation of a transcriptionally active macronucleus.
34 e found in markedly different numbers in the macronucleus.
35 d cells, with pronounced localization in the macronucleus.
36  During development of a micronucleus into a macronucleus after cell mating the IESs are excised from
37 estroyed when a micronucleus develops into a macronucleus after each cell mating.
38 sion of a micronucleus to a somatic nucleus (macronucleus) after cell mating, all IESs are excised fr
39                                      The old macronucleus already had been inactivated before most ac
40 ell contains both a transcriptionally active macronucleus and a germline micronucleus.
41 fter, pair separation, resorption of the old macronucleus, and elimination of one of the new micronuc
42 mall RNAs in both the old and the developing macronucleus, and is required for their stability.
43  Results of a parallel mapping effort in the macronucleus, and the correspondence between the two gen
44 ed from the genome of the developing somatic macronucleus, and the old parental macronucleus is degra
45  developmentally regulated excision from the macronucleus are discussed.
46 uences (MDSs), that give rise to the somatic macronucleus are interrupted by internal eliminated sequ
47     They do not form microtubules inside the macronucleus as normal cells do, and there is little or
48  to determine whether genomic mapping in the macronucleus by genetic means is feasible.
49 e are eliminated from the developing somatic macronucleus by specific DNA rearrangements.
50 pears from the centromeres in the developing macronucleus, consistent with centromeric sequences bein
51  nuclei: a somatic, transcriptionally active macronucleus containing hyperacetylated chromatin and a
52 e of the progeny; in contrast, the expressed macronucleus contains many copies of hundreds of small c
53 nthesis when expressed in the P. tetraurelia macronucleus, despite 24% primary sequence divergence of
54  IESs are AT-rich DNA segments that separate macronucleus-destined segments (MDSs) in micronuclear ge
55 have examined the chromatin structure of the macronucleus-destined sequences and Tec transposons, whi
56                                  Whereas the macronucleus-destined sequences show a typical pattern o
57 he parental macronucleus is degraded and new macronucleus develops from a mitotic product of the zygo
58                                          The macronucleus develops from the zygotic nucleus through a
59                                 Instead, the macronucleus divides by amitosis with random segregation
60 amecium IES, the presence of this IES in the macronucleus does not completely inhibit excision of its
61 t a partially functional Cbs retained in the macronucleus does not induce chromosome breakage during
62 n that accompanies breakdown of the parental macronucleus during conjugation, correcting the previous
63 rly in conjugation and in the new developing macronucleus during later developmental stages.
64 ly regulated as it moves into the micro- and macronucleus during the respective S phases.
65                It resides exclusively in the macronucleus during vegetative growth and is asymmetrica
66 res in the micronucleus but is absent in the macronucleus during vegetative growth.
67  CnjBp colocalize with Twi1p in the parental macronucleus early in conjugation and in the new develop
68 ion and segregation, the same markers in the macronucleus fall into coassortment groups (CAGs) under
69 ring the development of a polyploid, somatic macronucleus from a diploid germline micronucleus.
70 t occurs during differentiation of a somatic macronucleus from a germline micronucleus.
71 he development of a transcriptionally active macronucleus from a transcriptionally inert micronucleus
72 ation accompanies development of the somatic macronucleus from the germ-line micronucleus during the
73            During development of the somatic macronucleus from the germline micronucleus in ciliates,
74 sociated with differentiation of the somatic macronucleus from the germline micronucleus.
75                During the development of the macronucleus, germline chromosomes are rearranged throug
76                 The transcriptionally active macronucleus has about 50 copies of each chromosome.
77 genome shotgun sequencing of the Tetrahymena macronucleus has recently been completed at The Institut
78 th the mitotic micronucleus and the amitotic macronucleus in response to DSBs induced by chemical age
79 onuclear genome into the genome of a somatic macronucleus in Tetrahymena thermophila requires several
80                During the formation of a new macronucleus in the ciliate Euplotes crassus, micronucle
81 IES elements) eliminated from the developing macronucleus in the ciliate Tetrahymena thermophila are
82 us into the transcriptionally active somatic macronucleus in the ciliated protozoan Tetrahymena therm
83 y regulated excision during formation of the macronucleus in the ciliated protozoan TETRAHYMENA: Anal
84 s in the polyploid, transcriptionally active macronucleus, indicating that neither of the two genes i
85                           Development of the macronucleus involves massive genome remodeling, includi
86 d-type DNA content, division of the amitotic macronucleus is both delayed and abnormal.
87 ual reproduction (conjugation), the parental macronucleus is degraded and new macronucleus develops f
88 g somatic macronucleus, and the old parental macronucleus is degraded by an apoptotic mechanism.
89 m distribution of alleles in the Tetrahymena macronucleus is due to the random distribution of the MA
90                                          The macronucleus is transcriptionally active during vegetati
91                  Nucleotide diversity in the macronucleus is very high (SNP heterozygosity is approxi
92                                  The somatic macronucleus (MAC) and germline micronucleus (MIC) of Te
93 nuclei: the transcriptionally active somatic macronucleus (MAC) and the transcriptionally silent germ
94           The gene-sized DNA molecule in the macronucleus (mac) of Oxytricha nova (On) encoding heat-
95 ves as the genetic blueprint for the somatic macronucleus (MAC), which is responsible for all transcr
96 th a germline micronucleus (MIC) and somatic macronucleus (MAC).
97  the same cell--a micronucleus (MIC) and the macronucleus (MAC).
98 separately in the micronucleus (MIC) and the macronucleus (MAC).
99  and the actively expressed somatic nucleus (macronucleus [MAC])-within a common cytoplasm.
100 A copy number is unaffected in the polyploid macronucleus, mechanisms that prevent reinitiation appea
101                        Nonetheless, when the macronucleus of a pawn mutant (pwA/pwA) was injected wit
102 akage occurs during formation of the somatic macronucleus of ciliated protozoa.
103  trait: deletion elements present in the old macronucleus of one partner of a mating pair were suffic
104 fficult to clone since the 800-ploid somatic macronucleus of P. tetraurelia is a formidable obstacle
105  micronucleus and retention of others in the macronucleus of related species suggest an evolutionary
106  of DNA segments from the developing somatic macronucleus of Tetrahymena, yet how specific internal e
107                                          The macronucleus of the binucleate ciliate Tetrahymena therm
108                                          The macronucleus of the ciliate Tetrahymena thermophila cont
109 er of 30%, occurs in the developing amitotic macronucleus of the ciliate Tetrahymena thermophila.
110  50 copies of each chromosome in the somatic macronucleus of the ciliated protozoan TETRAHYMENA: Appr
111                                          The macronucleus of this ciliated protozoan contains 9,000 c
112  by identical sequences are expressed in the macronucleus, only the former undergoes mitochondrial im
113 nscriptional activation and retention in the macronucleus or heterochromatization and elimination.
114            During development of the somatic macronucleus, Oxytricha trifallax destroys 95% of its ge
115 icronucleus and the transcriptionally active macronucleus - provides a powerful means for controlling
116       Knockdown of CNA1 genes in the somatic macronucleus results in micronuclear DNA loss and delaye
117                   While sequences within the macronucleus-retained DNA are known to determine the exc
118 ive transcription products in the developing macronucleus; some even contain free-standing genes.
119 ly transcriptionally inactive, and a somatic macronucleus that contains a reduced, fragmented and rea
120 ventional mitosis and meiosis, and a somatic macronucleus that divides by an amitotic process.
121                    During development of the macronucleus the genome undergoes a series of reorganiza
122 ssive divisions of an initially heterozygous macronucleus, the random distribution of alleles of loci
123 issing sequences, and then allow the zygotic macronucleus to reproduce the same deletions.
124 omic library through microinjection into the macronucleus, we have isolated a DNA fragment that compl
125 s a localized, motile hub that traverses the macronucleus while replicating DNA.

 
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