ライフサイエンスコーパス: sex-determining gene

1 wn to be a duplicate of another Hymenopteran sex-determining gene.

2 ement in the fem-3 3'UTR and repressing this sex-determining gene.

3 tal proof that Sry was the elusive mammalian sex-determining gene.

4 ve linkage of sexually antagonistic genes to sex-determining genes.

5 n animals and fungi is regulated by specific sex-determining genes.

6 genetic programme that involves most of the sex-determining genes.

7 been produced of a plant chromosome carrying sex-determining genes.

8 f the AFLP markers and to locate the mutated sex-determining genes.

9 ution of new regulatory interactions between sex-determining genes and genes that control spatial pat

10 n for the observed preponderance of dominant sex determining genes, and hint that drift-induced selec

11 Thus, WNT-4, a novel sex-determining gene, and DAX1 play a concerted role in

12 ene may be the ancestral precursor of Sry, a sex-determining gene, and Sox3 has been proposed to play

13 tis and are thought to express Sry, the male sex-determining gene, and to play a crucial role in dire

14 on from hermaphroditism to monoecy, multiple sex determining genes are involved, including male-steri

15 tic interactions among FEM1, NOT1, and other sex-determining genes are described.

16 e upregulation of Sox9 in cases where female sex-determining genes are disrupted.

17 animal lineages are inevitably controlled by sex-determining genes, but the genetic basis of sexually

18 orphic sex chromosomes and rapid turnover of sex-determining genes can complicate establishing the se

19 Homeotic and sex-determining genes control a wide range of morphologi

20 Furthermore, X. laevis' sex-determining gene, DM-W, does not exist in X. tropica

21 ome, which initiates from the putative avian sex-determining gene DMRT1 and ends at the pseudoautosom

22 The role played by the sex-determining gene doublesex (dsx) and its influence o

23 tterns of expression of maternal and zygotic sex determining genes expected to result from conflict o

24 st intron of Fem1c, a gene homologous to the sex-determining gene fem-1 of Caenorhabditis elegans.

25 abditis elegans hermaphrodite germ line, the sex-determining gene fem-3 is repressed posttranscriptio

26 Sex-determining genes frequently exhibit sexually dimorp

27 is has also happened in honeybees, where the sex-determining gene has now been shown to be a duplicat

28 sperm families, the actual identification of sex-determining genes has been elusive, and their regula

29 tagonistic loci that are tightly linked to a sex-determining gene have a vastly stronger influence on

30 uences of alleles of the honey bee's primary sex-determining gene have extremely high diversity, with

31 Sex-determining genes have been identified in flies, wor

32 The sex-determining gene her-1 is required for male developm

33 C-2 associates with the promoter of the male sex-determining gene her-1 to repress its transcription.

34 ing a transgene activation system, the human sex-determining gene hSRY is activated in the single-cel

35 ether the expression of SOX9, a central male sex-determining gene in mammals, or three other conserve

36 strate that Dmrt1 is a candidate master male sex-determining gene in this TSD species, consistent wit

37 ggests the possible continued involvement of sex-determining genes in maintaining ovarian function th

38 discovery of many of the now-known mammalian sex-determining genes, including SRY, RSPO1, SOX9, NR5A1

39 indifferent until the transient action of a sex-determining gene initiates gonadal differentiation.

40 In Caenorhabditis elegans, the tra-2 sex-determining gene is regulated at the translational l

41 The fem-3 sex-determining gene is repressed post-transcriptionally

42 stic selection can cause the spread of a new sex-determining gene linked to it.

43 ermine whether interactions between multiple sex-determining genes might be partly responsible for th

44 In some taxa the master sex-determining gene moves frequently between chromosome

45 The tra-1 and tra-2 sex-determining genes promote female fates in Caenorhabd

46 mbination, which surrounds the male-specific sex-determining gene, remains very small, despite ancien

47 he initial expression of the female-specific sex-determining gene Sex-lethal in the blastoderm embryo

48 as a monomer to the regulatory region of the sex-determining gene SF1.

49 embryo in response to the expression of the sex determining gene, Sry, in Sertoli cell precursors.

50 n morphological event downstream of the male sex determining gene, Sry, is the induction of prolifera

51 stis development just downstream of the male sex-determining gene, Sry: (1) for the proliferation of

52 ning loci, the transposition of an ancestral sex-determining gene to an autosome, and the maintenance

53 se results significantly narrow the putative sex-determining gene to the very terminal region of the

54 The C. elegans sex-determining gene tra-2 is subject to multiple forms

55 The Caenorhabditis elegans sex-determining gene tra-2 promotes female development a

56 present in the 3' untranslated region of the sex-determining gene tra-2.

57 inized by a loss-of-function mutation in the sex-determining gene tra-3 results in masculinization of

58 In addition, the sex-determining gene, tra-3, appears to promote female d

59 es with the predicted activity of one of the sex-determining genes, TRANSFORMER5 (TRA5).

60 oogenesis relies on regulation of the fem-3 sex-determining gene via a regulatory element in the fem

61 Here, the locus for an autosomal sex-determining gene was mapped via linkage analysis in