IUBio GIL .. BIOSCI/Bionet News .. Biosequences .. Software .. FTP

I was unsuccessfuk with direct mail, Peter

fodoran at LUDENS.ELTE.HU fodoran at LUDENS.ELTE.HU
Sat Mar 25 12:58:00 EST 1995


From:	LUDENS::FODORAN      25-MAR-1995 16:58:37.88
To:	MX%"phunt at chiswick.anprod.CSIRO.AU"
CC:	FODORAN
Subj:	RE: strange patterns of inheritance

Dear Peter,


I dhave received a message of exactly the same text ... but my reply did not go
through. I have forwarded it to you, please let me know if arrived.

Shortly: I got comparable results when I crossed X-linked mutants of different
alleles of the same gene (dpy-8 e130 x dpy-8 e1321(ts).

Also, Dpy progeny segregated WT. Explanation: partial complementation in the
first, intragenic recombination in the second case.

If you use the same alleles, the genetic background of the parents may be
different. Some variations I can imagine (maybe wrong):

1.	An autosomic mutation which may remained in your X-any/X-any homozygous
strain which needed for the 100% expression in XX and X0 animals
homo(hemi)zygous for "any". If this mutation were DOMINANT, when you cross out
your homozygous lady-worms with a WT male, of course all male progeny is of ANY
as being heterozygous for this hypotetic dominant allele, let me call it Some.

So for a 100% penetration you need animals of any/any; Some/+ or
any/any;Some/Some or any/0; Some/+ or any/0; Some/Some genotypes.

When you cross back, half of the B1 progeny will be homozygous for
the recessive allele of Some, and LESS THAN 100% of your any/any; +/+
worms will be of ANY phenotypes.

But you did not mention what was the hermaphrodite/male ratio in your
cross. Neither the phenotypic ratio of the any/0 male progeny.

Can you speak about it?

2.	Mitochondrial gene under an autosomic mutation may also be involved.
What is the results of different reciprocal crosses?

(male progeny of any/any X +/0  cross; any/+ X any/0 male and hermaphrodite
progeny)?

3.	If I were you, I would make several OUTCROSSES first (in order to get
rid of the disturbing genetic background if I were interested only in any) and
then several backcrosses to have the missing data replacing my hypothetical
Some and mit genes.

I were extremely interested to know what wil be your final result and meet in
Madison with you.

Please reply.

		Andras Fodor



die not go thrhough.




More information about the Celegans mailing list

Send comments to us at archive@iubioarchive.bio.net